Multiple-Choice Questions in Organic Chemistry
Multiple choice questions
usually include a phrase or stem followed by three to five
options/choices.
Test strategies :
• Read the directions carefully
• Know if you are penalized for guessing
• Answer easy questions first
Answering options
:
• Improve your odds, think critically
• Hide the options, read the stem, and try to answer
Select the option that most closely
matches your answer
• Read the stem with each option
Treat each option
as a true-false question, and choose the “most true”
Strategies to answer difficult questions :
• Eliminate options you know to be incorrect
• Question options that are totally
unfamiliar to you
• Question options that contain negative
or absolute words
• “All of the above”
If you know two of the
three options seem correct, “all of the above”
is a strong possibility
• Number answers :
Toss out the high and low and consider
the middle range
numbers
• “Look alike options”
Probably one is correct; choose the best but eliminate
choices that mean basically the same thing, and thus
cancel each other out
• Echo options :
If two options are opposite
each other , chances are one of them is correct
• If two alternatives seem correct,
compare them for differences,
then refer to the stem to find your best answer
Guessing :
• Always guess when there is no penalty
for guessing
or you can eliminate options
• Don’t guess if you are penalized
for guessing
and if you have no basis for your choice
• Don’t change your answer
unless you are sure
of the correction
When taking a test you are demonstrating
your ability to understand your course material. Successful test taking avoids
carelessness. Stay relaxed and confident. Remind yourself that you are
well-prepared and going to do well. If you find yourself anxious, take several
slow, deep breaths to relax. Don’t talk about the tests to other students just before it; anxiety is contagious.
This unit includes 1000 multiple choice
questions. The purpose is to assess the breadth of student’s
knowledge and understanding of the basic concepts of organic chemistry. Remember that the
multiple choice questions :
1.
are not simply
definitions.
2. require application of recalled information, not simple recall.
3.
require fine distinctions between correct and nearly-correct statements.
4. emphasize conceptual understanding
These questions have been
especially designed to cover all the important concepts of organic chemistry.
Solve them carefully. You will be
glad that you did !
1. Which of the following
is not a characteristic of organic compounds?
(a) They usually
have low melting
points.
(b) They usually
are only slightly soluble or insoluble in water.
(c) If water soluble they seldom conduct an electric current.
(d) Bonds which bind
the atoms together are nearly always ionic.
Answer. (d)
2. The element least
likely to be found in an organic compound is
(a) oxygen
(b) sulfur
(c) nitrogen
(d) silicon
Answer. (d)
3. One of the major sources of organic compounds is
(a) Natural gas
(b) Fermentation
(c)
Sea water
(d) Atmosphere
Answer. (a)
4. Catenation is a property
of the carbon atom which describes its ability to
(a) bond with other carbon atoms
(b) form double
and triple bonds
(c) exist in plant and animal form
(d) form bonds
in its ground state
Answer. (a)
5. In stable organic compounds, carbon will always form
(a) 2 bonds
(b) 4 bonds
(c) 3 bonds
(d) 5 bonds
Answer. (b)
6. Carbon-carbon double
bonds consist of :
(a) one σ bond, one
Ï€ bond
(b) two σ bonds, one π bond
(c)
one σ bond, two π bonds
(d) two σ bonds, two π bonds
Answer. (a)
7. Acetylene has a total of :
(a) one σ bond, two π
bonds
(b) two σ bonds, four π
bonds
(c)
three σ bonds, two π bonds
(d) one σ bond, four π bonds
Answer. (c)
8. In propene
there are
(a) eight σ bonds and one π bond
(b) seven σ bonds and two π bonds
(c) six σ bonds and three π bonds
(d) nine σ bonds
Answer. (a)
9. In propyne
there are
(a) six σ bonds and two π bonds
(b) seven σ bonds and one π bond
(c) six σ bonds and one π bond
(d) eight σ bonds
Answer. (a)
10. 1-Buten-3-yne has
(a) six σ and four π
bonds
(b) seven σ and three π bonds
(c)
eight σ and two π bonds
(d) nine σ and one π bond
Answer. (b)
11. Compound in which carbons
use only sp3 hybrid orbitals
for bond formation
is
(a) CH3CH2CH3
(b) CH3C≡CH
(c) CH3CH=CH2
(d) CH2=CH—CH=CH2
Answer. (a)
12. Compound
in which carbon uses sp3 hybrid
orbitals for bond formation is (a)
(b)
(c)
(d) (CH3)3COH
Answer. (d)
13. When the carbon atom is sp2 hybridized in a compound,
it is bonded to
(a) 2 other atoms
(b) 4 other atoms
(c)
3 other atoms
(d) 5 other atoms
Answer. (c)
14. Compound in which carbons use only sp2 hybrid orbitals for bond formation is
(a)
(b)
(c)
CH2=CH–CH=CH2
(d) CH3CH=C=CH2
Answer. (c)
15. Which of the following
is a planar molecule?
(a) Formaldehyde
(b) Acetone
(c) Formic acid
(d) Acetic acid
Answer. (a)
16. What is bond angle between the hybrid orbitals
in methane?
(a) 180°
(b) 120°
(c) 109.5°
(d) 115.5°
Answer. (c)
17. The H–C–C bond angle in ethane is
(a) 60°
(b) 109.5°
(c) 120°
(d) 118°28′
Answer. (b)
18. The H–C–H bond angle in ethylene
is
(a) 60°
(b) 120°
(c)
90°
(d) 180°
Answer. (b)
19. What is the bond length of a carbon-carbon double bond?
(a) 1.20 Ã…
(b) 1.34 Ã…
(c)
1.54 Ã…
(d) 1.68 Ã…
Answer. (b)
20. The carbon-carbon bond lengths in rank of increasing bond length is :
(a) triple, double, single
(b) single, double, triple
(c)
single, triple, double
(d) triple, single,
double
Answer. (a)
21. Which of the following
is the correct order of bond lengths :
(a) C–C < C=C <
C≡C
(b) C–C > C≡C >
C=C
(c) C≡C > C–C >
C=C
(d) C≡C < C–C >
C=C
Answer. (a)
22. Which of the following
hydrocarbons has the shortest C–C bond
length?
(a) CH2=CH2
(b) CH3CH3
(c) HC≡CH
(d)
Answer. (c)
23. The carbon-carbon bond length is maximum in
(a) CH2=CH2
(b) CH3CH3
(c)
HC≡CH
(d)
Answer. (b)
24.
What is the hybridization of the
carbon atoms numbered 1 and 2 respectively in
the following structure?
(a) sp3, sp2
(b) sp2, sp2
(c) sp, sp
(d) sp2, sp
Answer. (d)
25. How many atoms are attached to an atom having
a sp hybridization?
(a) 0
(b) 1
(c) 2
(d) 3
Answer. (c)
26. Which statement
is true?
(a) Resonance hybrids are inherently unstable.
(b) Resonance hybrids are more stable than any individual resonance form.
(c)
Resonance hybrids are averages
of all resonance forms resembling the less stable forms.
(d)
Resonance hybrids are averages
of all resonance forms resembling
the more stable forms.
Answer. (d)
27. Resonance
structures of a molecule have
(a) same arrangement of atoms
(b) different arrangement of atoms
(c) same number
of paired electrons
(d) different number
of paired electrons
Answer. (a) and (c)
28. Which of the
following compounds have planar molecules?
(a) ethyl alcohol
(b) formaldehyde
(c)
diethyl ether
(d) 1,3-butadiene
Answer. (b) and (d)
29. Which of the following
compounds will show dipole moment?
(a) cis-1,2-dichloroethylene
(b) o-dichlorobenzene
(c) trans-1,2-dichloroethylene
(d) p-dichlorobenzene
Answer. (a) and (b)
30. Which molecule
has a nonzero dipole moment?
(a) Cl2
(b) CO2
(c) CCl4
(d) CHCl3
Answer. (d)
31. Which of the following
compounds have lowest
dipole moment?
(a) carbon tetrachloride
(b) chloromethane
(c) dichloromethane
(d) chloroform
Answer. (a)
32. Which molecule
has the greatest dipole moment
(a) CH3Cl
(b) CH3Br
(c)
CH3F
(d) CH3I
Answer. (c)
33. Which of the following
compounds have highest
dipole moment?
(a) dichloromethane
(b) chloroform
(c) chloromethane
(d) carbon tetrachloride
Answer. (a)
34. Homolytic fission
of C–C bond leads to the formation
of :
(a) Free radicals
(b) Carbonium ions
(c) Carbanions
(d) None of these
Answer. (a)
35. Homolytic fission
of covalent bond between carbon
atoms will produce :
(a) Two carbonium
ions
(b) Two molecules
(c) Free radicals
(d) Carbonium ion and carbanion
Answer. (c)
36. The order of stability
of carbonium ions is
(a) tertiary > secondary > primary
(b) secondary > tertiary > primary
(c)
primary > secondary
> tertiary
(d) primary > tertiary > secondary
Answer. (a)
37. The order of stability of carbanions is
(a) primary > secondary > tertiary
(b) secondary > tertiary > primary
(c)
tertiary > secondary
> primary
(d) tertiary > primary > secondary
Answer. (a)
38. Which of the following carbonium ions will
be most stable? (a)
(b)
(c)
(d)
Answer. (d)
39. The least stable carbanion
is :
(a)
(b)
(c)
(d)
Answer. (b)
40. Which alkyl free radical is the most stable?
(a) methyl
(b) primary
(c) secondary
(d) tertiary
Answer. (d)
41. Which of the following is an electrophile?
(a)
(b)
(c)
(d)
Answer. (b)
42. Which of the following
is not an electrophile?
(a) NH3
(b) Br+
(c) AlCl3
(d) NO2+
Answer. (a)
43. Which of the following
statements is correct
regarding nucleophiles?
(a) They have an overall
positive charge
(b) They have a lone-pair
of electrons
(c) They have an unpaired
electron
(d) They have empty orbitals
Answer. (b)
44. Which of the following
is a nucleophile?
(a) AlCl3
(b) H3O+
(c)
BF3
(d) CN–
Answer. (d)
45. Which of the following
is not a nucleophile?
(a) NH3
(b) HSO3–
(c) AlCl3
(d) HO–
Answer. (c)
46. Which of the
following is not a nucleophile? (a)
(b) BF3
(c)
(d) NH3
Answer. (b)
47. Which of the following
is a Lewis acid?
(a) AlCl3
(b) CH3OH
(c)
NH3
(d) CH3OCH3
Answer. (a)
48. Which of the
following ranges best represents the strength of a hydrogen
bond?
(a) 5-10 kcals
(b) 60-80 kcals
(c) 80-100 kcals
(d) 100-120 kcals
Answer. (a)
49. Which describes
the bond strength
or bond dissociation energy?
(a) energy required
to break a bond
(b) energy released
when a bond breaks
(c)
energy released when a bond is formed
(d) (a) and (c)
Answer. (d)
50. Which statement
is correct?
(a) Energy is released when a bond breaks.
(b) A sigma bond results
from attraction of protons and electrons.
(c) Energy is released when a bond forms.
(d) A carbanion is positively charged.
Answer. (c)
51. Which of the following
is incorrect?
(a)
Resonance stabilization is the extra stability
a compound gains from
having delocalized electrons.
(b) Delocalized electrons
destabilize a compound.
(c)
The greater the number of
relatively stable resonance contributors, the greater is the resonance stabilization.
(d) (a) and (c)
Answer. (b)
52. Which of the following
is correct?
(a)
Curved arrows are always
drawn from an electron poor center to an
electron rich center.
(b) A doubled headed arrow means one electron has been moved.
(c)
Curved arrows are always drawn from an
electron rich center
to an electron poor center.
(d) A single
headed arrow means two electrons
have been moved.
Answer. (c)
53. What does a “curved”
arrow represent?
(a) that two structures are resonance structures
(b) the movement
of two electrons
(c)
a link between
reactants and products
(d) that two structures are equivalent
Answer. (b)
54. What is the predicted shape, bond angle, and hybridization for CH3+?
(a) trigonal planar,
120°, sp2
(b) trigonal planar,
120°, sp3
(c) trigonal planar, 109.5°, sp2
(d) trigonal pyramidal, 120°, sp2
Answer. (a)
55. What
is the name given for a species that
contains a positively charged carbon
atom?
(a) carbanion
(b) carbocation
(c)
methyl radical
(d) free radical
Answer. (c)
56. What orbitals
overlap to create the H–C bond in CH3+?
(a) sp3–sp3
(b) sp2–sp3
(c) s–p
(d) s–sp2
Answer. (d)
57. The lone-pair
electrons of the methyl anion occupy a orbital.
(a) s
(b) sp
(c) sp2
(d) sp3
Answer. (d)
58.
An increase in which of the following results in a decrease in the
rate of the chemical reaction?
(a) temperature
(b) concentration
(c)
collision frequency
(d) energy of activation
Answer. (d)
59. The
reaction step that has its transition state at the highest point
on the reaction coordinate is the
called the .
(a) rate-determining step
(b) activation energy
(c)
transition step
(d) product favored
step
Answer. (a)
60. An electrophile acts as a when it reacts with a nucleophile.
(a) Bronsted-Lowry base
(b) Arrhenius base
(c)
Lewis acid
(d) Lewis base
Answer. (c)
61. A nucleophile acts as a when it reacts with an electrophile.
(a) Bronsted-Lowry acid
(b) Arrhenius base
(c) Lewis acid
(d) Lewis base
Answer. (d)
62. Which of the following
is not normally considered to be a nucleophile?
(a) NH3
(b) CH3NH2
(c) HC≡C:–
(d) CH3CH2+
Answer. (d)
63. Which of the following
is not a nucleophile?
(a) FeBr3
(b) Br–
(c) NH3
(d) CH3OCH3
Answer. (a)
64. Which of the following
is the strongest interaction?
(a) a covalent
bond
(b) dipole-dipole interactions
(c)
hydrogen bonding
(d) van der Waals
Answer. (a)
65. Which of the
following statements is incorrect?
(a) Electrons move toward positively charged locations.
(b) An electron-rich atom is called an electrophile.
(c) An electrophile is electron loving.
(d) A nucleophile has a a pair of electrons it can share.
Answer. (b)
66. Which of the following
is a nonpolar molecule?
(a) HCl
(b) CH3Cl
(c) H2
(d) NH3
Answer. (c)
67. Which is defined as a species
that accepts a proton?
(a) Lewis acid
(b) Lewis base
(c)
Bronsted-Lowry acid
(d) Bronsted-Lowry base
Answer. (d)
68. Which statement
is correct about
acid-base chemistry?
(a) the larger
the Ka, the stronger
the acid
(b) a small pKa correspond to a large Ka
(c)
the smaller the pKa, the stronger the acid
(d) all of the above
Answer. (d)
69. Which of the following
statements is correct?
(a) The stronger the acid, the weaker its conjugate base.
(b) The stronger
the acid, the stronger its conjugate base.
(c) The stronger
the base, the stronger its conjugate base.
(d) The stronger the acid, the weaker its conjugate acid.
Answer. (a)
70. What is the
conjugate acid of CH3NH2?
(a) CH3NH3+
(b) CH3NH–
(c) NH4+
(d) NH2–
Answer. (a)
71. What is the conjugate base of CH3NH2?
(a) CH3NH3+
(b) CH3NH–
(c)
NH4+
(d) NH2–
Answer. (b)
72. The stronger the
acid .
(a) the less stable its conjugate base
(b) the larger
the pKa
(c)
the weaker its conjugate base
(d) the larger
the pH
Answer. (c)
73. Which of the following
is the strongest acid?
(a) HI
(b) H2O
(c) CH4
(d) CH3OH
Answer. (a)
74. Which of the following
are Lewis bases?
(a) NF3
(b) BF3
(c) CH3OCH3
(d) (a) and (c)
Answer. (d)
75.
Two compounds have the same
composition and also have the same atoms attached to the same atoms, although
with different orientations in space. These compounds are
(a) Identical
(b) Position isomers
(c) Structural isomers
(d) Stereoisomers
Answer. (d)
76. The isomers of a substance must have
(a) same chemical properties
(b) same molecular
weight
(c) same structural formula
(d) same functional groups
Answer. (b)
77.
Compounds with the same molecular formula but different
structural formulas are called
(a) Alkoxides
(b) Iso compounds
(c) Isomers
(d) Ortho compounds
Answer. (c)
78. Ethanol (CH3CH2OH) and dimethyl
ether (CH3OCH3)
are best considered :
(a) structural isomers
(b) stereoisomers
(c) enantiomers
(d) diastereomers
Answer. (a)
79. The compounds CH3CH2OCH2CH3
and CH3OCH2CH2CH3 are
(a) Enantiomers
(b) Conformational isomers
(c) Metamers
(d) Optical isomers
Answer. (c)
80. Which of the following
statements is false about tautomers?
(a) Tautomers are structural isomers
(b) Tautomers are structural isomers which exist in dynamic equilibrium
(c) Tautomerism involves movement of atoms
(d) Tautomers have independent existence
Answer. (d)
81.
How many isomers are possible for the compound
with molecular formula C4H8?
(a) 2
(b) 4
(c) 6
(d) 8
Answer. (c)
82. How many structural isomers
are possible for C4H9Br?
(a) 2
(b) 3
(c) 4
(d) 5
Answer. (c)
83. How many isomeric aromatic
hydrocarbons are possible
for C8H10?
(a) 3
(b) 4
(c) 5
(d) 6
Answer. (b)
84. Which compound
is not an isomer of the other
three?
(a) n-Pentane
(b) 2,2-Dimethylpropane
(c)
2-Methylbutane
(d) 2,3-Dimethylbutane
Answer. (d)
85. Alkenes show geometrical isomerism
due to :
(a) Asymmetry
(b) Rotation around a
single bond
(c) Resonance
(d) Restricted rotation
around a double bond
Answer. (d)
86. Which of the following
compounds exhibit geometrical isomerism?
(a) 1-Pentene
(b) 2-Methyl-2-pentene
(c) 2-Pentene
(d) 2-Methyl-2-butene
Answer. (c)
87. Which of the following
compounds may exist as cis-trans isomers?
(a) 1-Butene
(b) 2-Butene
(c) Cyclopropane
(d) Acetone
Answer. (b)
88. Geometrical isomerism is shown by
(a) Lactic acid
(b) Maleic acid
(c)
1-Butene
(d) 1,1-Dichloroethylene
Answer. (b)
89. Which of the following
compounds show geometrical isomerism
(a) (CH3)3N
(b) CH3CH=CH2
(c) (CH3)2NH
(d) CH3CH=CHCH3
Answer. (d)
90. Which of the following
compounds will show geometrical isomerism?
(a) CH2=CHCl2
(b) ClCH=CHBr
(c) CH2=CHCl
(d) Cl2C=CBr2
Answer. (b)
91. Which of the following
compounds will not show geometrical isomerism?
(a) BrCH=CHBr
(b) BrCH=CHCl
(c)
(d)
Answer. (d)
92. A molecule
is said to be chiral
(a) if it contains plane of symmetry
(b) if it contains centre of symmetry
(c) if it cannot be superimposed on its mirror image
(d) if it can
be superimposed on its mirror image
Answer. (c)
93. Which of the statements is false regarding
chiral compounds?
(a) rotate the plane of polarized light
(b) have cis and trans isomers
(c) exist as enantiomers
(d) can be detected with a polarimeter
Answer. (b)
94. An optically
active compound
(a) must contain
atleast four carbons
(b) when in solution rotate
the plane of polarized light
(c)
must always contain an asymmetric carbon atom
(d) in solution
always give a negative reading
in polarimeter.
Answer. (b)
95. Plane-polarized light is
affected by
(a) Identical molecules
(b) All polymers
(c) Chiral molecules
(d) All biomolecules
Answer. (c)
96. It is possible to distinguish between
optical isomers
(a) by using
chemical tests
(b) by mass spectrometry
(c) by IR
spectroscopy
(d)
by polarimetry
Answer. (d)
97. Optical isomers that are mirror images are called :
(a) Tautomers
(b)
Diastereomers
(c) Enantiomers
(d) Metamers
Answer. (c)
98. Optical isomers that are not mirror images are called
(a) Diastereomers
(b)
Enantiomers
(c) Metamers
(d)
Meso compounds
Answer. (a)
99. Enantiomers have which of the following
characteristics?
(a)
rotate ordinary light
(b) have the same melting
point
(c) are superimposable mirror images
(d)
react with optically
active molecules at the same rate
Answer. (b)
100. Which of the following
statements is false about enantiomers?
(a) rotate plane-polarized light
(b) are superimposable mirror images
(c)
are nonsuperimposable mirror images
(d) have the same melting
point
Answer. (b)
101. A meso compound :
(a) is an achiral molecule
which contains chiral carbons
(b)
contains a plane
of symmetry or a
centre of symmetry
(c) is optically inactive
(d) is characterized by all of the above
Answer. (d)
102. What is the possible
number of optical isomers for a compound containing n
dissimilar asymmetric carbon
atoms?
(a)
n2
(b) 2n
(c)
n + 1
(d)
n + 2
Answer. (b)
103.
What is the possible number of
optical isomers for a compound containing 2
dissimilar asymmetric carbon atoms?
(a) 2
(b) 4
(c) 6
(d) 8
Answer. (b)
104. meso-Tartaric acid is
(a) sometimes optically
active
(b) always optically active
(c)
sometimes optically inactive
(d) always optically inactive
Answer. (d)
105. Which of the following
compounds will be optically active?
(a) Propanoic acid
(b)
3-Chloropropanoic
acid
(c) 2-Chloropropanoic acid
(d) 3-Chloropropene
Answer. (c)
106. Which of the following
compounds will be optically active?
(a) Succinic acid
(b)
meso-Tartaric acid
(d) Lactic acid
(d) Chloroacetic acid
Answer. (c)
107. Which of the following
isomeric compounds show optical isomerism
:
(a)
1-Aminopentane
(b) 2-Aminopentane
(c) 3-Aminopentane
(d)
2,2-Dimethylpropylamine
Answer. (b)
108. 2-Butanol is optically active because it contains :
(a)
an asymmetric carbon
(b) a plane of symmetry
(c)
a hydroxyl group
(d)
a centre of symmetry
Answer. (a)
109. Optical isomerism is shown by
(a) n-Butyl chloride
(b)
sec-Butyl chloride
(c) tert-Butyl chloride
(d) Isobutyl chloride
Answer. (b)
110. Which of the
following compounds is an optically
active compound? (a)
(b)
CHCl3
(c)
CH3CH2COOH
(d) CH3CH2OH
Answer. (a)
111. Lactic acid, ,
is a molecule which shows
(a) Geometrical isomerism
(b)
Tautomerism
(c) Optical isomerism
(d) Metamerism
Answer. (c)
112. How many optical isomers
are possible for lactic acid?
(a) 2
(b) 4
(c) 6
(d) 8
Answer. (a)
113. Which of the following
represents a racemic
mixture?
(a)
75% (R)-2-butanol, 25% (S)-2-butanol
(b) 25% (R)-2-butanol, 75% (S)-2-butanol
(c) 50% (R)-2-butanol, 50% (S)-2-butanol
(d)
none of the above
Answer. (c)
114.
Consider (R)- and (S)-2-butanol.
Which physical property distinguishes the two
compounds?
(a)
melting point
(b)
solubility in common solvents
(c) Rotation of plane-polarized light
(d)
Infrared spectrum
Answer. (c)
115. Which of the following
is capable of exhibiting cis-trans isomerism?
(a) 1-butene
(b) 1-pentene
(c)
ethene
(d) 2-butene
Answer. (d)
116. Which of the following
is a true statement?
(a) All chiral molecules possess a plane of symmetry.
(b)
All achiral molecules
are meso.
(c)
All molecules which possess a single asymmetric center of the
S configuration are levorotatory.
(d)
A mixture of achiral compounds
will be optically inactive.
Answer. (d)
117. Which of the statements below correctly describes
an achiral molecule?
(a) The molecule has a nonsuperimposable mirror image.
(b)
The molecule exhibits optical
activity when it interacts with
plane-polarized light.
(c)
The molecule has an enantiomer.
(d) The molecule
might be a meso form.
Answer. (d)
118.
How many asymmetric centers are present in a molecule of 2,4,6- trimethylheptane?
(a) 0
(b) 1
(c) 2
(d) 3
Answer. (a)
119. Which of the following
compounds is never chiral?
(a) 2,3-dibromobutane
(b)
1,3-dibromobutane
(c) 1,2-dichlorobutane
(d) 1,4-dibromobutane
Answer. (d)
120.
Which of the following statements is correct concerning a pair of enantiomers?
(a)
They rotate the plane of polarized light by exactly
the same amount
and in opposite directions.
(b)
They rotate the plane of polarized
light by differing amounts and in opposite directions.
(c)
They rotate the plane of polarized light by differing amounts and in the same direction.
(d)
They have different melting points.
Answer. (a)
121. Which of the following
is not true of enantiomers?
(a)
They have the same melting
point.
(b) They have the
same boiling point.
(c) They have the same density.
(d)
They have the same
specific rotation.
Answer. (d)
122.
A and B are stereoisomers. They are
nonsuperimposable and are mirror images of one another. Which of the following
best describes the relationship between A and B?
(a)
structural isomers
(b) enantiomers
(c)
cis-trans isomers
(d) diastereomers
Answer. (b)
123. Which of the
statements is correct about diastereomers?
(a) They are stereoisomers that are not enantiomers.
(b)
They are a pair of identical isomers.
(c) They are a pair of isomers
that are mirror images.
(d) All their asymmetric centers are the same.
Answer. (a)
124. Which of the following
is/are optically inactive?
(a)
a 50-50 mixture
of R and S enantiomers
(b) a meso compound
(c) a racemic mixture
(d)
all the above
Answer. (d)
125. Hydrocarbons are
(a) Composed of carbon and hydrogen
(b) Composed of carbon, hydrogen,
and oxygen
(c)
Composed of carbon
and oxygen
(d) Composed of carbon and nitrogen
Answer. (a)
126. Hydrocarbons are
(a) insoluble in
water
(b) composed of carbon and hydrogen
(c) both (a) and (b)
(d) None of these
Answer. (c)
127. Which of following statements is false about propane?
(a) all bond angles are 109.5°
(b) each carbon
is sp3 hybridized
(c) the compound
is combustible
(d) the compound
undergoes polymerization to give polypropylene.
Answer. (d)
128. Which of the
following is a correct name according to the IUPAC rules?
(a) 2-Methylcyclohexane
(b) 2-Ethyl-2-methylpentane
(c)
3,4-Dimethylpentane
(d) 3-Ethyl-2-methylpentane
Answer. (d)
129. A tertiary
carbon is bonded directly to :
(a) 2 hydrogens
(b) 3 carbons
(c)
2 carbons
(d) 4 carbons
Answer. (b)
130. What type of an alkyl group is
an isobutyl group?
(a) primary
(b) secondary
(c) tertiary
(d) none of these
Answer. (a)
131. Which molecular formula indicates 2-methylpentane?
(a) C5H12
(b) C6H14
(c) C5H10
(d) C6H12
Answer. (b)
132. Which molecular
formula indicates 2,2,4-trimethylhexane?
(a) C9H20
(b) C9H18
(c)
C8H18
(d) C8H16
Answer. (a)
133. How many isomers are possible for butane?
(a) 2
(b) 3
(c) 4
(d) 5
Answer. (a)
134. How many isomers are possible for 2-methylpropane?
(a) 2
(b) 3
(c) 4
(d) 5
Answer. (a)
135. How many isomers are possible for pentane?
(a) 2
(b) 3
(c) 4
(d) 5
Answer. (b)
136. How many isomers are possible for hexane?
(a) 4
(b) 5
(c) 6
(d) 7
Answer. (b)
137. How many isomers are possible for heptane?
(a) 9
(b) 10
(c) 11
(d) 12
Answer. (a)
138. Marsh gas mainly contains
(a) CH2=CH2
(b) CH4
(c) H2S
(d) CHCl3
Answer. (b)
139. Which statement
is false?
(a) Many alkanes are soluble in water.
(b) All alkanes have a lower density
than water.
(c)
At room temperature some alkanes are liquids, some solids, some gases.
(d) All alkanes
burn.
Answer. (a)
140.
As
the molecular weight of
alkanes increases, how do the boiling point and melting point
change?
(a) boiling point increases ; melting point
increases.
(b) boiling point increases ; melting point
increases.
(c) boiling point
increases ; melting
point decreases
(d)
boiling point increases ; melting
point increases sequentially for alkanes over
four carbons.
Answer. (d)
141. The branching of alkanes that produces symmetrical structures :
(a) raises the boiling point ; raises the melting
point
(b) raises the boiling point ; lowers the melting
point
(c) lowers the boiling point ; lowers the melting
point
(d) lowers the boiling point ; raises the melting
point
Answer. (a)
142. How does the
melting point of propane and ethane
compare?
(a) the melting point of propane
is greater.
(b) the melting
point of ethane is greater.
(c) the melting
points are within 5°C of one another.
(d) no relationship exists among these alkanes and their melting
points.
Answer. (b)
143. How do the
boiling points of butane, propane,
and ethane compare?
(a) the boiling point of ethane is greatest.
(b) the boiling point of butane is greatest.
(c) the boiling
point of propane is greatest.
(d) there is no relationship
among these three alkanes and their boiling points.
Answer. (b)
144. Which of the following
alkanes will have the highest boiling point?
(a) n-Octane
(b) Isopentane
(c)
n-Butane
(d) Neopentane
Answer. (a)
145. Which of the following
alkanes will have the lowest boiling point?
(a) n-Heptane
(b) Isopentane
(c) n-Hexane
(d) Neopentane
Answer. (d)
146. Methane can be prepared
by :
(a) the reaction
of iodomethane with sodium in dry ether
(b) the reaction
of methanol with concentrated H2SO4
(c) the reaction
of sodium methanoate with soda-lime
(d) the reaction
of sodium ethanoate with soda-lime
Answer. (d)
147. Which of the following
reactions can be used to prepare alkanes?
(a) Corey-House synthesis
(b) Williamson synthesis
(c) Friedel-Crafts reactions
(d) None of these
Answer. (a)
148. Which of the following
reactions can be used to prepare alkanes?
(a) Wurtz reaction
(b) Wolf-kishner reduction
(c)
Kolbe's electrolysis
(d) All of these
Answer. (d)
149. Kolbe's electrolysis of sodium butyrate gives
(a) C8H16
(b) C6H14
(c)
C8H18
(d) C6H12
Answer. (b)
150.
Which of the following classes of
compounds is unreactive toward sulfuric acid?
(a) Alkanes
(b) Alcohols
(c)
Alkenes
(d) Alkynes
Answer. (a)
151.
Which of the following compounds
does not dissolve in concentrated H2SO4
on warming?
(a) n-Hexane
(b) Diethyl ether
(c) 1-Butene
(d) Aniline
Answer. (a)
152. 2,3-Dimethyl-2-butene undergoes
catalytic hydrogenation to give
(a) 2,3-Dimethylbutane
(b) 2-Methylpentane
(c)
2,2-Dimethylbutane
(d) 3-Methylpentane
Answer. (a)
153. Why is the halogenation of alkanes considered a chain reaction?
(a) it occurs quickly.
(b) it occurs without the generation of intermediates.
(c) each step generates the reactive intermediate that causes the next step to
occur.
(d) the reaction
allows long chains of halogenated alkanes to be formed.
Answer. (c)
154. The chlorination of methane
to give CCl4 is an example of
(a) an electrophilic addition
(b) a free-radical substitution
(c) a nucleophilic addition
(d) an electrophilic substitution
Answer. (b)
155.
In
the chlorination of alkanes, the first step in which chlorine free radicals
are produced is called :
(a) initiation
(b) activation
(c)
propagation
(d) deactivation
Answer. (a)
156. Chlorine free radicals react with methane
by :
(a) donating their free-radical electron
to methane to form chloromethane.
(b)
abstracting a hydrogen atom from
methane, and producing HCl and a
methyl radical.
(c)
forming a carbanion intermediate that rapidly dissociates to produce
chloromethane.
(d)
forming a carbonium ion intermediate that rapidly
dissociates to form chloromethane.
Answer. (b)
157.
Which halogen does not appreciably react with methane
in a free-radical substitution reaction?
(a) chlorine
(b) bromine
(c) iodine
(d) fluorine
Answer. (c)
158. What product
is formed in the free-radical bromination of methane?
(a) bromomethane
(b) dibromomethane
(c) tribromomethane
(d) all of these
Answer. (d)
159. Chlorination of an alkane
as compared to bromination proceeds
(a) at a slower rate
(b) at a faster rate
(c)
with equal rates
(d) with equal or different
rate depending upon the source of alkane.
Answer. (b)
160.
How many monochlorinated isomers
would result from the reaction
of chlorine with n-butane in
the presence of UV light?
(a) 2
(b) 4
(c) 6
(d) 8
Answer. (a)
161.
How many monochlorination products
are possible in the reaction
of 2,2- dimethylbutane with
chlorine in the presence of ultraviolet light?
(a) 2
(b) 3
(c) 4
(d) 5
Answer. (a)
162.
A
compound of formula
C3H8 does not react with bromine in CCl4 in the dark. The compound could be
(a) Alkane
(b) Cycloalkane
(c) Alkene
(d) Cycloalkene
Answer. (a)
163. The combustion of Pentane produces
:
(a) Pentene
(b) HCl + H2O
(c)
Pentyne
(d) CO2 + H2O
Answer. (d)
164.
The combustion of one
mole of propane, C3H8,
produces how many moles of H2O?
(a) 2
(b) 3
(c) 4
(d) 5
Answer. (c)
165.
The major carbon compound formed from
the incomplete combustion of a
hydrocarbon in air is
(a) carbon dioxide
(b) carbon monoxide
(c) water
(d) alkyl chains
Answer. (b)
166. The thermal decomposition of alkanes in the absence
of air is called :
(a) Combustion
(b) Oxidation
(c) Cracking
(d) Hydrogenation
Answer. (c)
167. LPG (Household cooking gas) is mainly
a mixture of
(a) Methane + Ethane
(b) Acetylene + O2
(c) Butane + Isobutane
(d) Acetylene + H2
Answer. (c)
168. What type of bonding
is most important in CH3CH2CH2CH2CH2CH3?
(a) ionic
(b) hydrogen
(c)
covalent
(d) polar
Answer. (c)
169.
What is the name given to a compound
containing only carbons
and hydrogens and having the
maximum number of hydrogens in the molecule?
(a) alkene
(b) unsaturated hydrocarbon
(c) saturated hydrocarbon
(d) alkyne
Answer. (c)
170.
Which of the following
is the best description of propane,
CH3CH2CH3, at room temperature?
(a) liquid, soluble
in H2O
(b) gas, soluble in gasoline
(c) liquid, soluble in gasoline
(d) gas, soluble in water
Answer. (b)
171.
Choose the correct hybridization for the atom indicated in the molecule below.
(a) sp
(b) sp2
(c) sp3
(d) none of these
Answer. (c)
172. Which of the following
has the greatest solubility in CH3CH2CH2CH3?
(a) CH3OH
(b) CH3NH2
(c)
CH3OCH3
(d) (CH3)3CH
Answer. (d)
173.
Consider the three isomeric alkanes
n-hexane, 2,3-dimethylbutane, and 2-
methylpentane. Which of the following correctly
lists these compounds in order
of increasing boiling point?
(a) 2,3-dimethylbutane < 2-methylpentane < n-hexane
(b) 2-methylpentane < n-hexane < 2,3-dimethylbutane
(c) 2-methylpentane < 2, 3-dimethylbutane < n-hexane
(d) n-hexane < 2-methylpentane < 2,3-dimethylbutane
Answer. (a)
174. The eclipsed
and staggered forms of ethane are said to differ in .
(a) molecular formula
(b) configuration
(c)
conformation
(d) constitution
Answer. (c)
175. Octane number is
related to
(a) Gasoline
(b) Kerosene oil
(c)
Diesel oil
(d) Lubricating oil
Answer. (a)
176. A knocking
sound is produced
in the engine when the
fuel
(a) Burns fast
(b) contains lubricating oil
(c) Burns slow
(d) contains water
Answer. (a)
177. The octane rating of gasoline provides information on
(a) its antiknock properties
(b) its ignition
properties
(c)
its percentage proportion
of octane
(d) its percentage content of isooctane
Answer. (a)
178.
In any fuel, the percentage by
volume of isooctane in a mixture of isooctane and n-heptane which will knock under same conditions as the fuel being
tested, is called :
(a) Cracking
(b) Iodine number
(c) Aromatization
(d) Octane number
Answer. (d)
179. Which of the following
compounds is assigned the Octane Number of zero :
(a) n-Octane
(b) 2,3,3-Trimethylpentane
(c)
n-Heptane
(d) 2,2,4-Trimethylpentane
Answer. (c)
180. Which of the following
compounds is assigned the Octane Number of 100 :
(a) n-Heptane
(b) 2,3,3-Trimethylpentane
(c) n-Octane
(d) 2,2,4-Trimethylpentane
Answer. (d)
181.
Gasoline with an octane number of 90 is equivalent in knocking characteristics to a mixture
of heptane and isooctane of the following
composition
:
(a) 20% heptane + 80% isooctane
(b) 90% heptane + 10% isooctane
(c) 80% heptane + 20% isooctane
(d) 10% heptane + 90% isooctane
Answer. (d)
182. A fuel with octane
number 90 means it is as good as a mixture of :
(a) 90% Isooctane
+ 10% n-heptane
(b) 90% n-Heptane + 10% isooctane
(c) 2 Litre of 90% isooctane + 2 litre of benzene
(d) 2 Litre of 90% n-heptane + 2 litre of benzene
Answer. (a)
183.
Which hydrocarbon molecule with eight carbons would produce the lowest
octane number (i.e., the most knocking) when
used as a fuel in automobile?
(a) 2-Methyl-3,3-dimethylpentane
(b) n-Octane
(c) 2-Isopropylpentane
(d) 2-Methylheptane
Answer. (b)
184. Which of the
following compounds is used as an antiknock compound?
(a) Ethyllithium
(b) Tetraethyllead
(c)
Ethyl acetate
(d) Lead acetate
Answer. (b)
185.
Which of the following methods can
be used to increase the octane rating of gasoline?
(a) Adding branched-chain alkanes
(b) Adding tetraethyllead
(c) Adding aromatic
hydrocarbons
(d) All of these
Answer. (d)
186. The carbon atoms involved in the double bond of an alkene are
(a) sp hybridized
(b) sp2 hybridized
(c)
sp3 hybridized
(d) None of these
Answer. (b)
187. Which of the following
compounds will show geometrical isomerism?
(a) Propene
(b) 2-Butene
(c)
Propyne
(d) 2-Butyne
Answer. (b)
188. Which of the following compounds is most stable?
(a) Ethylene
(b) 2,3-Dimethyl-1-butene
(c)
Propylene
(d) 2-Butene
Answer. (b)
189. In which
solvent are alkenes most soluble?
(a) water
(b) ethyl alcohol
(c) ammonia
(d) carbon tetrachloride
Answer. (d)
190.
Which statements about alkenes and
alkanes of corresponding chain lengths is
true?
(I)
Alkenes have slightly
lower melting points than alkanes
(II)
Alkenes have slightly
higher melting points
than alkanes
(III)
Alkenes have higher
boiling points than alkanes
(IV)
Alkenes have lower boiling points
than alkanes
(a) I and III
(b) II and IV
(c)
I and IV
(d) II and
III
Answer. (a)
191.
How do the melting points of trans isomers compare to the cis isomers for alkenes?
(a) cis isomers have
higher melting points
(b) trans isomers have higher melting points
(c) both have similar melting
points
(d) no consistent trend is observed
Answer. (b)
192. Why do trans isomers of alkenes have lower boiling
points than cis isomers?
(a) trans isomers have better symmetry
(b) cis isomers have better symmetry
(c) trans isomers are less polar
(d) cis isomers are less polar
Answer. (c)
193. The major product of acid-catalyzed dehydration of 3-pentanol is :
(a) 1-Pentene
(b) 2-Methyl-1-butene
(c)
2-Pentene
(d) 3-Methyl-1-butene
Answer. (c)
194. Ethylene is obtained from ethyl bromide
by :
(a) Simple heating
(b) Hydrolysis
(c) Dehydrohalogenation
(d) Nucleophilic substitution
Answer. (c)
195.
The dehydrohalogenation of 2-bromobutane with alcoholic KOH gives
mainly
(a) 2-Butene
(b) 2-Butyne
(c)
1-Butene
(d) 1-Butyne
Answer. (a)
196. In the reaction of propene with HCl, H+ ion acts as the :
(a) electrophile
(b) carbonium ion
(c) nucleophile
(d) carbanion
Answer. (a)
197.
When bromine attacks the double bond in propene, which of the following
ions is formed in the first stage of the attack?
(a)
(b)
(c)
(d)
Answer. (a)
198.
In the reaction of ethylene with
H2O in the presence of sulfuric acid, which one adds
across the double bond first?
(a) H+
(b) H.
(c) HO–
(d) sulfate ion
Answer. (a)
199.
Why does a H+ ion attacking a
carbon-carbon double bond add to the carbon with the least number of
substituents?
(a) the reaction
is resonance stabilized.
(b) the hybrid
geometry favors this process.
(c) nucleophile tends to
attack stable centers of negative
charge.
(d) a more stable carbonium
ion is generated.
Answer. (d)
200.
Propene reacts with bromine
to form 1,2-dibromopropane. This is an example of
(a) Nucleophilic addition
(b) Electrophilic addition
(c)
Nucleophilic substitution
(d) Electrophilic substitution
Answer. (b)
201. Baeyer's reagent
is
(a) dilute KMnO4
(b) HCl + ZnCl2
(c) Br2 in CCl4
(d) NH2NH2
Answer. (a)
202.
In the addition of HX to a double
bond, the hydrogen goes to the carbon that already has more hydrogens is a
statement of
(a) Hund's rule
(b) Markovnikov's rule
(c)
Huckel rule
(d) Saytzeff rule
Answer. (b)
203. Markovnikov's addition
of HBr is not applicable to
(a) Propene
(b) 1-butene
(c) 1-pentene
(d) 2-butene
Answer. (d)
204.
In the reaction of CH3CH2CH=CH2
with HCl, the H of the HCl will become attached to which carbon?
(a) C-1
(b)
C-2
(c) C-3
(d)
C-4
Answer. (a)
205.
Which of the following compounds will react most readily with bromine in CCl4?
(a)
CH3CH2CH3
(b)
(CH3)3CH
(c) CH3CH=CH2
(d)
(CH3)4C
Answer. (c)
206.
The disappearance of the purple
color of KMnO4 in its reaction with alkene is known as
(a)
Markovnikov test
(b) Grignard test
(c)
Baeyer test
(d) Wurtz test
Answer. (c)
207.
Which of the following will give a negative test when treated with bromine in carbon tetrachloride?
(a)
Butane
(b) 2-Butene
(c)
1,3-Butadiene
(d) 2-Butyne
Answer. (a)
208. Ethylene reacts with HI to give
(a) Iodoethane
(b) 2,2-Diiodoethane
(c)
1,1-Diiodoethane
(d) None of these
Answer. (a)
209. Which of the following
reagents will react with propene?
(a) Hot alkaline
KMnO4
(b)
Sodium metal
(c) Cold dilute HNO3
(d) LiAlH4
Answer. (a)
210. Which of the following
compounds will have zero dipole moment?
(a) cis-1,2-dibromoethylene
(b)
1,1-dibromoethylene
(c) trans-1,2-dibromoethylene
(d)
all of these
Answer. (c)
211. 2-Methylpropene reacts with HBr to give
(a)
tert-Butyl bromide
(b) Isobutane
(c) n-Butyl bromide
(d)
None of these
Answer. (a)
212. 2-Butene reacts with HBr to give
(a) 1-Bromobutane
(b) 2,3-Dibromobutane
(c)
2-Bromobutane
(d) 2,2-Dibromobutane
Answer. (c)
213.
Which of the following alkenes
reacts with HBr in the presence of a peroxide to give anti-Markovnikov's product?
(a)
1-Butene
(b) 2,3-Dimethyl-2-butene
(c) 2-Butene
(d)
3-Hexene
Answer. (a)
214. Propene reacts with HBr in the presence of a peroxide to give
(a)
n-Propyl bromide
(b) Allyl bromide
(c)
Isopropyl bromide
(d) Vinyl bromide
Answer. (a)
215. 2-Methylpropene reacts with HBr in the presence of peroxide to give
(a) A primary
alkyl bromide
(b) A secondary alkyl bromide
(c)
A tertiary alkyl bromide
(d) A vicinal
dibromide
Answer. (a)
216. 2-Methyl-2-butene reacts with HBr in the presence of peroxide to give
(a) A primary
alkyl bromide
(b)
A secondary alkyl bromide
(c) A tertiary
alkyl bromide
(d)
A vicinal dibromide
Answer. (b)
217. Hydration of 2-methyl-1-propene (with H2O/H2SO4) gives :
(a)
CH3CH2CH2OH
(b) (CH3)3COH
(c) CH3CH2CH2CH2OH
(d)
(CH3)2CHOH
Answer. (b)
218.
A
compound reacts with steam in the
presence of concentrated H2SO4 to give isopropyl alcohol.
The compound could be
(a)
Alkane
(b)
Alkyne
(c) Alkene
(d)
Allene
Answer. (c)
219. Propene reacts with Cl2 in H2O to give
(a)
1-Chloro-2-propanol
(b) 2-Chloro-2-propanol
(c) 1-Chloro-1-propanol
(d)
2-Chloro-1-propanol
Answer. (a)
220. 1-Butene reacts with Cl2 in H2O to give
(a)
1-Chloro-2-butanol
(b) 2-Chloro-2-butanol
(c)
1-Chloro-1-butanol
(d) 2-Chloro-1-butanol
Answer. (a)
221. Catalytic hydrogenation of 3-methyl-1-butene gives :
(a) Isobutane
(b) 2,2-Dimethylbutane
(c)
2-Methylbutane
(d) 2,3-Dimethylbutane
Answer. (c)
222.
Which of the following alkenes gives
only acetic acid on oxidation with hot concentrated KMnO4.
(a)
Ethylene
(b) 1-Butene
(c)
Propene
(d) 2-Butene
Answer. (d)
223.
Which of the following
compounds will give only acetaldehyde on ozonolysis?
(a)
1-Butene
(b) Acetylene
(c) 2-Butene
(d)
Ethylene
Answer. (c)
224.
Which of the following alkenes will give a mixture of acetone and formaldehyde on ozonolysis?
(a)
2-butene
(b)
2-methyl-2-butene
(c) 1-butene
(d) 2-methylpropene
Answer. (d)
225.
Which of the following alkenes will give a mixture of acetone and acetaldehyde an ozonolysis?
(a)
1-butene
(b) 2-methyl-2-butene
(c)
2-butene
(d) 2-methylpropene
Answer. (b)
226.
A
hydrocarbon, C6H12,
on ozonolysis gives only one product which does not give silver mirror with
Tollens' reagent. The hydrocarbon is
(a)
2,3-Dimethyl-2-butene
(b) 2-Hexene
(c) 2-Methyl-2-pentene
(d)
3-Hexene
Answer. (a)
227. Combustion of an alkene with sufficient oxygen will produce
(a) carbon dioxide
and water
(b)
carbon monoxide and
water
(c) only carbon
dioxide
(d)
only carbon monoxide
Answer. (a)
228.
Which of the following
are correct statements concerning unsaturated
hydrocarbons?
(a)
All unsaturated hydrocarbons are insoluble in water.
(b)
All unsaturated hydrocarbons are soluble in nonpolar solvents.
(c) All unsaturated hydrocarbons are more dense than water.
(d)
(a) & (c)
Answer. (d)
229. How many electrons are involved in a carbon-carbon double bond?
(a) 1
(b) 2
(c) 3
(d) 4
Answer. (d)
230. Which of the following statements about ethene,
C2H4, is incorrect?
(a) The H–C–H bond angles are approximately 109.5°.
(b) There is a total of five sigma bonds.
(c)
The carbon atoms are sp2 hybridized.
(d) The H–C–H bond angles are approximately 120°.
Answer. (a)
231. Which of the following
statements about propene,
CH3CH=CH2, is
correct?
(a) All nine atoms
lie in the same plane.
(b) The compound has a
cis and trans isomer.
(c)
There is a
total of eight sigma bonds.
(d) All the carbon atoms are sp2 hybridized.
Answer. (c)
232. Which of the following
is capable of exhibiting cis-trans isomerism?
(a) 1-butene
(b)
1-pentene
(c) ethene
(d) 2-butene
Answer. (d)
233. Which of the following
is the most stable alkene?
(a)
trans-3-hexene
(b)
cis-3-hexene
(c) 1-hexene
(d)
(Z)-3-hexene
Answer. (a)
234.
Which of the alkyl chlorides listed
below undergoes dehydrohalogenation in the presence of a strong base to give 2-pentene as the only alkene product?
(a)
1-chloropentane
(b)
2-chloropentane
(c) 3-chloropentane
(d)
1-chloro-2-methylbutane
Answer. (c)
235.
What is the major product from the
acid-catalyzed hydration of 2-methyl-2- pentene?
(a)
2-methylpentane
(b) 2-methyl-1-pentanol
(c)
2-methyl-2-pentanol
(d) 2-methyl-3-pentanol
Answer. (c)
236. 1,2-Butadiene has
(a) only sp hybridized carbon atoms
(b)
only sp2 hybridized carbon atoms
(c) only sp3 hybridized carbon atoms
(d) sp, sp2, sp3 hybridized carbon atoms
Answer. (d)
237. How many σ (sigma)
bonds are there in CH2=CH—CH=CH2?
(a) 3
(b) 6
(c) 9
(d) 12
Answer. (c)
238. Propadiene, CH2=C=CH2, is
(a)
a planar compound
(b) a cumulated diene
(c)
an isolated diene
(d) a conjugated diene
Answer. (b)
239. Which of the following compounds have planar molecules?
(a)
1,3-Butadiene
(b) Dimethyl ether
(c)
1-Butene
(d) Allene
Answer. (a)
240.
Which of the following
molecular formulas will correspond to an alkene with two double bonds?
(a)
C4H10
(b) C5H12
(c)
C6H10
(d) C8H16
Answer. (c)
241. 1,3-Butadiene reacts with bromine
to mainly give
(a) 3,4-Dibromo-1-butene
(b) 4-Bromo-1-butene
(c)
1,4-Dibromo-2-butene
(d) 1-Bromo-2-butene
Answer. (c)
242.
What descriptive term is applied to the type of diene represented by 1,5-
octadiene?
(a)
conjugated diene
(b) cumulated diene
(c) isolated diene
(d)
alkynyl diene
Answer. (c)
243.
What descriptive term is applied to the type of diene represented by 2,4-
hexadiene?
(a)
conjugated diene
(b)
cumulated diene
(c) isolated diene
(d)
alkynyl diene
Answer. (a)
244.
Which of the following
statements are correct
concerning delocalized electrons?
(a)
Electrons do not belong to a single atom.
(b) Electrons are not confined
to a bond between two atoms
(c)
Electrons are shared by three or more atoms.
(d)
(a), (b) and (c)
Answer. (d)
245. What is the hybridization of the central carbon of allene (1,2-propadiene)?
(a) sp
(b)
sp2
(c) sp3
(d) p
Answer. (a)
246.
What compound results from the
1,4-addition of one equivalent of HBr to 1,3-butadiene?
(a)
1-bromo-1-butene
(b) 2-bromo-2-butene
(c)
4-bromo-1-butene
(d) 1-bromo-2-butene
Answer. (d)
247. Rank the following dienes in order of increasing stability :
trans-1, 3-pentadiene, cis-1,3-pentadiene,
1,4-pentadiene and 1,2-pentadiene. Answer. 1,2-pentadiene < 1,4-pentadiene < cis-1,3-pentadiene < trans-1,3- pentadiene
248. A triple bond consists of
(a) 2 sigma bonds
and 1 pi bond
(b)
3 sigma bonds
(c) 1 sigma bond
and 2 pi bonds
(d) 3 pi bonds
Answer. (c)
249.
The bond angles associated with the hybrid orbitals of a carbon involved in a triple bond is
(a)
180°
(b) 120°
(c)
109°
(d) 45°
Answer. (a)
250. How many electrons are involved in a carbon-carbon triple bond?
(a) 1
(b) 2
(c) 3
(d) 6
Answer. (d)
251.
Which of the following improperly
describes the physical
properties of an alkyne?
(a)
relatively nonpolar
(b)
nearly insoluble in water
(c) less dense than water
(d) insoluble in most organic
solvents
Answer. (d)
252.
Which of the following statements
correctly describes the general reactivity of alkynes?
(a)
An alkyne is an electron-rich molecule and therefore
reacts as a nucleophile.
(b)
The σ bonds of alkynes are higher
in energy than the bonds and are
thus more reactive.
(c)
Unlike alkenes, alkynes
fail to undergo electrophilic addition
reactions.
(d)
Alkynes are generally
more reactive than alkenes.
Answer. (d)
253. Which of the following describes
a triple bond?
(a)
two sigma bonds and two pi bonds
(b) one sigma
bond and one pi bond
(c) two sigma bonds
and one pi bond
(d)
one sigma bond and two pi bonds
Answer. (d)
254.
What two atomic orbitals
or hybrid atomic orbitals overlap
to form the carbon-carbon σ bond in ethyne?
(a)
sp3–sp3
(b)
sp2–sp2
(c) s–s
(d) sp–sp
Answer. (d)
255. Which of the following statements is not true
about propyne, HC–C≡CH3?
(a)
It contains six sigma bonds.
(b) It contains
three pi bonds.
(c) The H–C–H bond angle
is about 109.5°.
(d)
The C–C–C bond
angle is 180°.
Answer. (b)
256. How many distinct terminal
alkynes exist with a molecular formula
of C5H8?
(a) 1
(b) 2
(c) 3
(d) 4
Answer. (b)
257. How many distinct internal
alkynes exist with a
molecular formula of C6H10?
(a) 1
(b) 2
(c) 3
(d) 4
Answer. (c)
258. Which is the correct
order of decreasing acidity
in the following compounds?
A. H2O B. CH3CH3 C. NH3 D. CH2=CH2 E. HC≡CH
(a)
A > E > C > D >
B
(b) A > E > D >
B > C
(c) E > A > C
> B > D
(d)
A > C > E > D > B
Answer. (a)
259.
Which of the following compounds is the major product
when 1-hexyne is treated with
excess HBr?
(a)
1,1-dibromohexane
(b)
1,1-dibromohexene
(c) 1,2-dibromohexene
(d) 2,2-dibromohexane
Answer. (d)
260. The reagent
needed to convert
2-butyne to cis-2-butene is :
(a) H2/Pt
(b)
H2/Lindlar’s catalyst
(c) Li/NH3
(d)
Na/NH3
Answer. (b)
261.
Among the compounds water, 1-butyne, 2-butyne,
and ethane, which are
stronger acids than ammonia?
(a)
1-butyne and ethane
(b)
water and 1-butyne
(c) water and ethane
(d) 1-butyne and 2-butyne
Answer. (b)
262. What is the product
when 3-heptyne reacts
with the Lindlar
catalyst?
(a) 2-methyl-2-heptene
(b)
trans-3-heptene
(c) cis-2-methyl-3-hexene
(d)
cis-3-hexene
Answer. (d)
263.
In
the addition of hydrogen bromide
to alkynes, which of the following
species is believed to be an intermediate?
(a)
vinyl anion
(b)
vinyl cation
(c) vinyl radical
(d) carbene
Answer. (b)
264.
Starting with 2-butene, which of the following is the best method for preparing
2-butyne?
(a)
HBr; H2/Ni; Zn/H+
(b) HBr; Zn/H+; H2/Ni
(c)
Br2/CCl4;
Zn/H+; H2/Ni
(d)
Br2/CCl4; 2NaNH2
Answer. (d)
265.
In the following hydrogenation reactions ;
The hybrid state of the
carbon atom changes from (a)
(b)
(c)
(d)
Answer. (b)
266. Which of the following
hydrocarbons has acidic hydrogens?
(a) 1-Butene
(b)
1-Butyne
(c) 2-Butene
(d) 2-Butyne
Answer. (b)
267. Lindlar's catalyst is
(a)
LiAlH4
(b) Pd/BaSO4 in Quinoline
(c)
NH2NH2
(d) HCl/ZnCl2
Answer. (b)
268.
The higher reactivity of an alkene or alkyne, as compared to an alkane, is due to
(a)
sigma bonds
(b) pi bonds
(c)
hydrogen bonds
(d) None of these
Answer. (b)
269. Which of the following statements about alkenes
and alkynes is correct?
(a) Alkynes are reduced more readily than alkenes.
(b) Alkynes are reduced less readily than alkenes.
(c)
Alkynes and alkenes are reduced with equal speed.
(d) Alkynes and alkenes can not be reduced.
Answer. (a)
270. Which of the following
sequences regarding acid-strength is correct?
(a) HC≡CH > CH3CH2OH > CH3COOH
(b)
HC≡CH > CH3COOH > CH3CH2OH
(c) CH3COOH > HC≡CH > CH3CH2OH
(d) CH3COOH > CH3CH2OH > HC≡CH
Answer. (d)
271. 1,2-Dichloroethane reacts with excess
of NaNH2 to form
(a) Vinyl chloride
(b)
Ethylene
(c) Ethyl chloride
(d)
Acetylene
Answer. (d)
272. Propyne is formed
by
(a)
Polymerization of acetylene
(b) Reaction of acetylene with methane
(c) Reaction of acetylene with methyl chloride
(d)
Reaction of sodium
acetylide with methyl
chloride
Answer. (d)
273. Which of the following compounds on hydrolysis gives acetylene?
(a)
CaC2
(b) Mg2C3
(c)
Al4C3
(d) Cu2Cl2
Answer. (a)
274. Which of the
following compounds on hydrolysis gives propyne?
(a) CaC2
(b)
Mg2C3
(c) Al4C3
(d) Cu2Cl2
Answer. (c)
275.
Which one of the following
compounds will (a) decolorizes dilute
cold KMnO4 ; (b)
decolorizes bromine water ; and (c)
gives a white precipitate with ammoniacal AgNO3 solution.
(a)
1-Hexene
(b) 1-Hexyne
(c)
2-Hexene
(d) 2-Hexyne
Answer. (b)
276. Ethylene and acetylene can be distinguished by using
(a) Bromine in CCl4
(b)
Tollens' reagent
(b) Baeyer's reagent
(d) Phenylhydrazine
Answer. (b)
277. 1-Butyne can be distinguished from 2-butyne by using
(a) potassium permanganate
(b)
bromine in CCl4
(c) Tollens' reagent
(d)
chlorine in CCl4
Answer. (c)
278. 1-Butyne reacts
with
(a)
NaNH2
(b) Dil H2SO4 and HgSO4
(c) HBr
(d)
All of these
Answer. (d)
279. Propyne can be converted
to propene by using
(a) H2 + Lindlar's
catalyst
(b)
NH2NH2
(c) H2 + Pt catalyst
(d)
NH2NH2 + KOH
Answer. (a)
280.
2-Butyne undergoes catalytic hydrogenation in the presence
of Lindlar's catalyst to give
(a)
2-Butene
(b)
Butane
(c) 1-Butene
(d) 2-Methylpropene
Answer. (a)
281. Addition of two moles of HCl to propyne gives :
(a) 2,2-Dichloropropane
(b)
1,3-Dichloropropane
(c) 1,2-Dichloropropane
(d)
None of these
Answer. (a)
282. Propyne reacts with aqueous
H2SO4 in the presence
of HgSO4 to form
(a)
acetone
(b) 1-propanol
(c) acetaldehyde
(d)
2-propanol
Answer. (a)
283.
Acetylene reacts with water in the presence of sulfuric acid and mercuric sulfate to give
(a)
Acetone
(b)
Acetic acid
(c) Formaldehyde
(d) Acetaldehyde
Answer. (d)
284.
Which of the following
compounds will react with ammoniacal silver nitrate?
(a)
1-Butene
(b) 1-Butyne
(c)
2-Butene
(d)
2-Butyne
Answer. (b)
285.
Which of the following compounds
does not react with ammoniacal AgNO3 solution?
(a)
Acetylene
(b) 1-Butyne
(c) Propyne
(d)
2-Butyne
Answer. (d)
286.
Which of the following compounds
reacts with ammoniacal cuprous
chloride to give a precipitate?
(a)
1-Butene
(b)
1-Butyne
(c) 2-Butene
(d) 2-Butyne
Answer. (b)
287. Ozonolysis of 2-butyne gives
(a)
Formic acid
(b) Propanoic acid
(c) Acetic acid
(d)
Butanoic acid
Answer. (c)
288.
Which alkyne yields propanoic acid
as the only product upon treatment with ozone followed by hydrolysis?
(a)
1-Butyne
(b)
2-Hexyne
(c) 1-Pentyne
(d) 3-Hexyne
Answer. (d)
289. When acetylene
is passed through
hot iron tube at 400°C, it gives
(a)
Benzene
(b) Toluene
(c) o-Xylene
(d)
Mesitylene
Answer. (a)
290. When propyne
is passed through hot iron tube at 400°C, it gives
(a)
Benzene
(b)
Toluene
(c) m-Xylene
(d)
Mesitylene
Answer. (d)
291. The monomer
for Neoprene is
(a) Isoprene
(b) acrylonitrile
(c)
Chloroprene
(d) 1,3-butadiene
Answer. (c)
292.
A compound, C4H6,
reacts with bromine and forms a white precipitate with ammoniacal silver
nitrate solution. It reacts with dilute H2SO4
in the presence of mercuric sulfate to form 2-butanone. The compound could be
(a)
1-Butyne
(b) 1-Butene
(c) 2-Butyne
(d)
2-Butene
Answer. (a)
293.
Which of the following correctly
ranks the cycloalkanes in order of increasing ring strain per methylene?
(a)
cyclopropane < cyclobutane < cyclohexane < cycloheptane
(b)
cyclohexane < cyclopentane < cyclobutane < cyclopropane
(c) cyclopentane < cyclobutane < cyclopentane < cyclopropane
(d) cyclopentane < cyclopropane < cyclobutane < cyclohexane
Answer. (b)
294.
Which of the following
has two equatorial alkyl substituents in its most stable
conformation?
(a)
1,1-dimethylcyclohexane
(b) cis-1,2-dimethylcyclohexane
(c)
cis-1,3-diethylcyclohexane
(d) cis-1,4-diethylcyclohexane
Answer. (c)
295.
Which one of the following is not
a metal catalyst for the
hydrogenation of an alkene?
(a) Pd
(b) Pt
(c) Na
(d) Ni
Answer. (c)
296.
What is(are) the product(s) in the Pd-catalyzed hydrogenation of 1,2- dimethylcyclopentene?
(a)
trans-1,2-dimethylcyclopentane
(b) cis-1,2-dimethylcyclopentane
(c) a mixture of trans and cis-1,2-dimethylcyclopentane
(d)
1,1-dimethylcyclopentane
Answer. (b)
297. Which of the following
is not a possible reaction
of a carbocation?
(a) addition of a nucleophile
(b) rearrangement to a
more stable carbocation
(c)
addition of a proton to form an alkane
(d) loss of a β-hydrogen
to form an alkene
Answer. (c)
298.
Addition of HCl to 3-methyl-1-pentene gives
two products. One of
these is 2-chloro-3-methylpentane.
What is the other product?
(a)
1-Chloro-3-methylpentane
(b) 3-Chloro-3-methylpentane
(c) 3-Chloro-2-methylpentane
(d)
2-Chloro-2-methylpentane
Answer. (b)
299. Predict which
of the following alkenes reacts the fastest with HCl?
(a)
CH3CH2CH2CH2CH=CH2
(b) cis-CH3CH2CH=CHCH2CH3
(c)
trans-CH3CH2CH=CHCH2CH3
(d) (CH3)2C=CHCH2CH3
Answer. (d)
300. The hydroboration-oxidation reaction can be characterized as the
to an alkene.
(a) anti-Markovnikov
syn addition of water
(b)
anti-Markovnikov anti addition of water
(c) Markovnikov syn addition of water
(d)
Markovnikov anti addition of water
Answer. (a)
301.
A
compound, C15H24,
is reacted with excess hydrogen using a
metal catalyst. One equivalent of the compound
consumed three equivalents of hydrogen. How
many rings did the original compound
have?
(a) 1 only
(b)
2 only
(c) 3 only
(d)
None of these
Answer. (a)
302.
The reaction of 1-butene
with bromine, Br2, in aqueous solution
gives primarily
1- bromo-2-butanol.
Identify the nucleophilic species in the reaction.
(a) Br2
(b)
Br–
(c)
H2O
(d) HOBr
Answer. (c)
303.
Which brief statement most
accurately describes why alkenes react the
way they do?
(a)
C=C double bonds are weak.
(b)
A π bond is lost but a stronger σ bond is gained.
(c) C=C double bonds are unstable.
(d) C=C π bonds are attacked by nucleophiles.
Answer. (b)
304.
Which of the following poisonous
gas is formed when chloroform is exposed to light and air?
(a)
Mustard gas
(b) Carbon monoxide
(c)
Phosgene
(d) Chlorine
Answer. (c)
305. Freon-12, CCl2F2, is used as a
(a) Local anesthetic
(b)
Dry-cleaning agent
(c) Refrigerant
(d) Disinfectant
Answer. (c)
306.
Which of the following compounds
has been suggested as causing depletion of the ozone layer in the upper
stratosphere?
(a)
CH4
(b)
CCl2F2
(c) CF4
(d)
CH2Cl2
Answer. (b)
307.
Which of the following reagents
cannot be used to prepare an alkyl chloride from an alcohol?
(a)
HCl + ZnCl2
(b)
SOCl2
(c) NaCl
(d)
PCl5
Answer. (c)
308. 2-Propanol reacts with KBr and concentrated H2SO4 to give
(a)
1-Bromopropane
(b) 1,2-Dibromopropane
(c) 2-Bromopropane
(d)
2,2-Dibromopropane
Answer. (c)
309. The best way to prepare 1,2-Dibromoethane is to treat :
(a) Ethylene with Br2
(b) Acetylene with excess of HBr
(c)
Ethylene with excess of HBr
(d) 1,2-Dichloroethane with Br2
Answer. (a)
310. Alkyl halides
undergo
(a) Electrophilic substitution reactions
(b) Electrophilic addition
reactions
(c)
Nucleophilic substitution reactions
(d) Nucleophilic addition
reactions
Answer. (c)
311. n-Propyl iodide reacts with sodium
ethoxide to give :
(a) CH3CH2OCH2CH3
(b)
CH3CH2OCH2CH2CH3
(c) CH3CH2OCH3
(d) CH3OCH2CH2CH3
Answer. (b)
312. 1-Bromobutane reacts with alcoholic
KOH to mainly give
(a)
1-Butene
(b)
2-Butene
(c) 1-Butanol
(d)
2-Butanol
Answer. (b)
313. 2-Bromobutane reacts alcoholic KOH to
mainly give
(a) 1-Butene
(b) 2-Butene
(c)
1-Butanol
(d) 2-Butanol
Answer. (b)
314. Isopropyl bromide reacts with alcoholic KOH to give
(a) Propene
(b)
Isopropyl alcohol
(c) Propane
(d) n-Propyl alcohol
Answer. (a)
315. 2,2-Dichloropropane reacts with aqueous KOH to give
(a) 2,2-Propanediol
(b)
Propanal
(c) Acetone
(d)
Propene
Answer. (c)
316. 1,1-Dichloropropane reacts with aqueous KOH to give
(a)
1,1-Propanediol
(b) Acetaldehyde
(c) Propanone
(d)
Propyne
Answer. (b)
317.
Which of the following
compounds will not give a white precipitate with alcoholic AgNO3.
(a)
Bromobenzene
(b)
1-Bromopropane
(c) Ethyl bromide
(d)
2-Bromopropane
Answer. (a)
318.
Which of the following
compounds will give a white precipitate with alcoholic AgNO3?
(a)
Vinylbenzene
(b) Chlorobenzene
(c) Vinyl chloride
(d)
Allyl chloride
Answer. (d)
319. Carbylamine test involves heating
a mixture of
(a) alcoholic KOH, methyl iodide, and sodium
metal
(b) alcoholic KOH, methyl iodide,
and primary amine
(c)
alcoholic KOH, chloroform, and primary amine
(d) alcoholic KOH, methyl alcohol, and primary amine
Answer. (c)
320. When chloroform is heated with aqueous NaOH, it gives
(a) Formic acid
(b)
Sodium formate
(c) Acetic acid
(d) Sodium acetate
Answer. (b)
321. Which alkyl halides react most readily by nucleophilic substitution?
(a) CH3CH2Cl
(b)
CH3CH2I
(c) CH3CH2Br
(d) CH3CH2F
Answer. (b)
322.
Which of the following factors
influence whether a reaction will proceed by
an SN1, SN2, E1, or E2 mechanism?
(a)
Structure of the alkyl halide
(b) Solvent
(c)
Concentration of reagents
(d) Nature of the nucleophile
(e)
All of these
Answer. (e)
323. Which compound
reacts most rapidly
by an SN1 mechanism?
(a)
Methyl chloride
(b)
Isopropyl chloride
(c) Ethyl chloride
(d)
tert-Butyl chloride
Answer. (d)
324.
Which of the following
compounds would react most rapidly
in an SN2 reaction?
(a)
CH3CH2I
(b)
CH2=CH–I
(c) (CH3)2CHI
(d)
(CH3)3CI
Answer. (a)
325.
There are 8 isomers that have the
molecular formula C5H11Br.
How many of these are tertiary alkyl
bromides?
(a) 1
(b) 2
(c) 3
(d) 8
Answer. (a)
326. Which of the following
statements is correct for a saturated
alkyl halide?
(a)
the C–X bond results from overlap
of the s orbital of carbon and the p orbital of the halogen
(X)
(b)
the C–X bond results from overlap of the p orbital of carbon and
the p orbital of the halogen (X)
(c) the C–X bond results
from overlap of the sp3 orbital of carbon
and the p
orbital of the halogen (X)
(d) the C–X bond results
from overlap of the sp2 orbital of carbon
and the p
orbital of the halogen (X)
Answer. (c)
327.
Which of the following best describes the carbon-chlorine bond of an alkyl chloride?
(a)
nonpolar; no dipole
(b) polar; δ+ at carbon and δ– at chlorine
(c) polar; δ– at carbon and δ+ at chlorine
(d)
ionic
Answer. (b)
328. Which of the following
is a secondary alkyl halide?
(a) CH3Br
(b)
(CH3)3CBr
(c) (CH3)2CHBr
(d)
(CH3)2CHCH2Br
Answer. (c)
329. How should
CH3CHClCH2CH3 be classified?
(a) primary alkyl halide
(b) secondary alkyl halide
(c)
tertiary alkyl halide
(d) quarternary alkyl halide
Answer. (b)
330. Which of the following
will have the lowest boiling
point?
(a) CH3Cl
(b)
CH4
(c) CH2Cl2
(d) CHCl3
Answer. (b)
331.
Which of the following is not correct concerning substitution and
elimination reactions of alkyl halides?
(a)
The electrophile replaces
the leaving group.
(b)
Compounds containing
electron-donating groups bonded to an sp3 hybridized carbon undergo substitution and elimination
reactions.
(c)
The electronegative atom is
replaced by another atom or group in substitution reactions.
(d)
(a) and (b)
Answer. (d)
332.
Which of the following statements
concerning SN2 reactions of alkyl halides is not correct?
(a)
The rate of reaction depends
on the concentration of the nucleophile.
(b)
The rate of reaction depends
on the concentration of the alkyl halide.
(c)
The rate of reaction
of a particular alkyl bromide
depends on the steric
accessibility of the carbon of the C-Br bond.
(d)
All alkyl iodides react more rapidly than all alkyl chlorides.
Answer. (d)
333. Which of the following
correctly reflects relative
stabilities of carbocations?
(a) 3° allylic > 2° > 1° benzylic
(b)
methyl > 2° benzylic > 3°
(c) 3° benzylic > vinyl > 1°
(d)
2° allylic > 2° > vinyl
Answer. (d)
334. Which of the following
species is most reactive in a SN2 reaction?
(a) CH3CH2Cl
(b)
CH3CH2Br
(c) CH3CH2I
(d) CH3CH2F
Answer. (c)
335. Which of the following
is the best leaving group?
(a) F–
(b)
Cl–
(c) Br–
(d)
I–
Answer. (d)
336. Which of the following
is the strongest nucleophile in an aqueous solution?
(a)
HO–
(b) Cl–
(c) Br–
(d)
I–
Answer. (d)
337. Which of the following
is the best nucleophile in water?
(a) I–
(b) CH3SCH3
(c)
CH3OCH3
(d) Cl–
Answer. (a)
338.
Which of the following
compounds will undergo
an SN2 reaction
most readily?
(a)
(CH3)3CCH2I
(b) (CH3)3CCl
(c) (CH3)2CHI
(d)
(CH3)2CHCH2CH2CH2I
Answer. (d)
339. Which of the following
is the rate law for SN1 mechanisms?
(a)
Rate = k[Alkyl
Halide] [Nucleophile]
(b) Rate = k[Nucleophile]
(c)
Rate = k[Alkyl
Halide]
(d)
Rate = k1[Alkyl Halide] + k2[Nucleophile]
Answer. (c)
340. Which of the following
factors has no effect on the rate of SN1 reactions?
(a) the nature
of the alkyl halide
(b)
the nature of the leaving
group
(c) the concentration of the alkyl
halide
(d) the concentration of the nucleophile
Answer. (d)
341. Which is the most reactive alkyl halide in a SN1 reaction?
(a) CH3F
(b)
CH3Br
(c) CH3I
(d)
CH3Cl
Answer. (c)
342.
Which of the following
halides is most reactive in an E2 reaction with sodium
methoxide?
(a)
(CH3)3CCH2I
(b) (CH3)2CHCHICH3
(c) (CH3)2CHCH2Br
(d)
(CH3)2CHCH2Cl
Answer. (b)
343.
Which of the following
halides is least reactive in an E2 reaction with sodium methoxide?
(a)
(CH3)3CCH2I
(b)
(CH3)2CHCHICH3
(c) (CH3)2CHCH2Br
(d) (CH3)2CHCH2Cl
Answer. (a)
344.
Dehydrohalogenation of 2-bromobutane in the presence
of a strong base proceeds via which of the following mechanistic pathways?
(a)
SN1
(b) SN2
(c)
E1
(d) E2
Answer. (d)
345. Which of the alkyl chlorides listed below undergoes dehydrohalogenation in
the presence
of a strong base to give 2-pentene
as the only alkene product?
(a) 1-chloropentane
(b)
2-chloropentane
(c) 3-chloropentane
(d)
1-chloro-2-methylbutane
Answer. (c)
346.
Predict the two most likely mechanisms for the reaction of 2-iodohexane
with sodium ethoxide.
(a)
SN2 and SN1
(b)
E1 and E2
(c) SN2 and E2
(d) E1 and SN1
Answer. (c)
347.
Predict the two most likely
mechanisms which occur when 2-iodohexane is heated in ethanol.
(a)
SN2 and SN1
(b) E1 and E2
(c)
SN2 and E2
(d) E1 and SN1
Answer. (d)
348. Grignard reagents
do not show any reaction with
(a) Alkoxyalkanes
(b) Alkanones
(c)
Alkyl alkanoates
(d) Acyl halides
Answer. (a)
349. The Grignard
reagent, CH3CH2MgBr, can be used to prepare
(a) Ethane
(b)
3-Ethyl-3-pentanol
(c) Propanoic acid
(d) All of these
Answer. (d)
350.
Which is the best reagent to accomplish the following conversion?
(a)
Conc. H2SO4
(b) Na
(c)
Conc. HCl
(d)
Mg, then H2O
Answer. (d)
351.
What is the major product of the following
reaction?
(a)
1-Butanol
(b) Butanal
(c)
2-Butanol
(d) Butanone
Answer. (c)
352.
Ethylmagnesium iodide reacts with formaldehyde to give a
product which on acid-hydrolysis forms :
(a)
an aldehyde
(b) a primary
alcohol
(c) a ketone
(d)
a secondary alcohol
Answer. (b)
353.
Ketones react with Grignard reagents to form
an addition product which on hydrolysis gives a
(a)
Primary alcohol
(b)
Tertiary alcohol
(c) Secondary alcohol
(d) Ketal
Answer. (b)
354.
n-Propylmagnesium
bromide on treatment with carbon
dioxide and further hydrolysis gives :
(a)
Acetic acid
(b) Propanoic acid
(c)
Butanoic acid
(d) Formic acid
Answer. (c)
355.
Which of the following compounds
will react with methylmagnesium iodide followed by acid-hydrolysis to give
ethyl alcohol?
(a)
Ethylene
(b) Acetaldehyde
(c) Formaldehyde
(d)
Acetone
Answer. (c)
356.
Which of the following gives a tertiary alcohol when treated with
Grignard reagents?
(a)
(b)
(c)
(d) None of these
Answer. (c)
357.
Which of the following
compounds will react with methylmagnesium bromide to give tert-butyl alcohol?
(a)
Acetyl chloride
(b) Acetone
(c) Isopropyl alcohol
(d)
Acetaldehyde
Answer. (b)
358.
Phenylmagnesium bromide
reacts with acetaldehyde to form an addition product which undergoes acid-hydrolysis to
give
(a)
Diphenylcarbinol
(b)
Benzyl alcohol
(c) Methylphenylcarbinol
(d) Benzoic acid
Answer. (c)
359. Which of the following
is the strongest base?
(a) HOMgBr
(b)
H2O
(c) CH3OH
(d)
CH3MgBr
Answer. (d)
360. Which of the following
is correct?
(a)
When a Grignard reagent
reacts with a ketone, the addition product
is a primary alcohol.
(b)
When a Grignard reagent
reacts with a ketone, the addition product
is a secondary alcohol.
(c)
When a Grignard reagent
reacts with a aldehyde, the addition product
is a tertiary alcohol.
(d)
None of the above are correct.
Answer. (d)
361.
Which of the following alcohols can be prepared by the reaction
of methyl formate with excess
Grignard reagent?
(a)
1-pentanol
(b)
2-pentanol
(c) 3-pentanol
(d)
2-methyl-2-pentanol
Answer. (c)
362.
The number of structural isomers of alcohols
with molecular formula C3H7OH
is
(a) 5
(b) 4
(c) 3
(d) 2
Answer. (d)
363.
The number of structural isomers of alcohols
with molecular formula C4H9OH
is
(a) 5
(b) 4
(c) 3
(d) 6
Answer. (b)
364.
Why do alcohols have boiling points much higher than hydrocarbons of similar molecular
weight?
(a)
Alcohols have greater van der Waals attraction
forces.
(b) Alcohol molecules
have greater molecular
symmetry.
(c) Hydrogen bonds must be broken in the process of volatilization.
(d)
Alcohols must overcome
greater ionic forces in the process of volatilization.
Answer. (c)
365.
The high boiling points
of alcohols, as compared to the corresponding alkanes, are due to
(a)
Hydrogen bonding
(b)
Heavy oxygen atom
(c) Water solubility
(d)
None of these
Answer. (a)
366. Which of the
following has the highest boiling point?
(a) diethyl ether
(b)
n-Butyraldehyde
(c) n-propyl chloride
(d) n-Butyl alcohol
Answer. (d)
367. Which of the
following has the highest boiling point?
(a) CH3CH2CH2CH2Cl
(b)
HOCH2CH2CH2CH2OH
(c) CH3CH2CH2CH2OH
(d)
CH3CH2OCH2CH3
Answer. (b)
368.
Which of the following compounds has the highest boiling
point? (a)
(b)
CH3CH2CH2OH
(c)
(d)
CH3CH2OCH3
Answer. (b)
369. Which of the
following has the highest boiling point?
(a) CH3CH2OH
(b)
CH3CH2CH2CH2OH
(c) CH3OH
(d) CH3CH2CH2OH
Answer. (b)
370.
Rank the following substances in
order of increasing boiling point (lowest → highest):
(1) CH3CH2CH2CH2OH, (2) (CH3)2CHOCH3, (3) (CH3)3COH
(a) (1) < (2) < (3)
(b)
(2) < (1) < (3)
(c) (2) < (3) < (1)
(d)
(3) < (2) < (1)
Answer. (c)
371. Which of the following
compounds is the least soluble
in water?
(a) HOCH2CH2OH
(b)
CH3CH2CH2OH
(c) CH3CH2OH
(d)
CH3CH2CH2CH2OH
Answer. (d)
372. Methanol is known as :
(a)
Rubbing alcohol
(b) Grain alcohol
(c) Wood alcohol
(d)
Denatured alcohol
Answer. (c)
373. Rectified spirit
is
(a) 100% Ethanol
(b) 90% Ethanol
(c)
100% Methanol
(d) 95% Ethanol
Answer. (d)
374. Grain alcohol
is another name for
(a) Methyl alcohol
(b)
Isopropyl alcohol
(c) Ethyl alcohol
(d) n-Propyl alcohol
Answer. (c)
375. Lucas reagents
is
(a) HCl/NaNO2
(b)
H2/Pd
(c) HCl/ZnCl2
(d)
H2/Pd/BaSO4
Answer. (c)
376. Lucas test is used to determine the type of
(a)
alcohols
(b) acids
(c) amines
(d)
carbohydrates
Answer. (a)
377. Which of the following
gives positive Iodoform
test :
(a)
1-Propanol
(b) 2-Propanol
(c)
3-Propanol
(d) None of these
Answer. (b)
378. Which of the following
reagents will replace
–OH group by a halogen atom?
(a) HOCl
(b)
Br2
(c) SOCl2
(d) I2
Answer. (c)
379. The compound
which reacts most readily with Lucas reagent
is
(a)
CH3CH2Cl
(b) (CH3)2CHOH
(c) CH3CH2OH
(d)
(CH3)3COH
Answer. (d)
380.
Which of the following
compounds reacts slowest
with Lucas reagent
at room temperature?
(a)
1-butanol
(b)
2-propanol
(c) 2-butanol
(d) 2-methyl-2-propanol
Answer. (a)
381. Which of the following
compounds will react fastest with Lucas reagent?
(a) 1-propanol
(b)
2-methyl-1-propanol
(c) 2-propanol
(d)
2-methyl-2-propanol
Answer. (d)
382. Which of the following
compounds reacts fastest
with HBr?
(a)
1-propanol
(b) 2-methyl-1-propanol
(c) 2-propanol
(d)
2-methyl-2-propanol
Answer. (d)
383. When ethanol is treated
with sodium metal :
(a)
Sodium ethoxide is formed
(b) The sodium is oxidized
(c)
The acidic hydrogen
in reduced
(d) All these occur
Answer. (d)
384.
Which of the following alcohols will give a yellow
precipitate of iodoform with
iodine and dilute NaOH solution?
(a)
1-Propanol
(b) 2-Propanol
(c)
1-Butanol
(d) 2-Methyl-2-propanol
Answer. (b)
385. Ethyl alcohol can react with concentrated H2SO4 to give
(a) Ethylene
(b) Diethyl ether
(c)
Ethyl hydrogen sulfate
(d) All of these
Answer. (d)
386. Ethanol on heating with concentrated H2SO4 at 170°C gives
(a) ethylene
(b)
ethyl hydrogen sulfate
(c) diethyl ether
(d) diethyl sulfate
Answer. (a)
387. The major product of acid-catalyzed dehydration of 2-butanol is :
(a) 2-Butene
(b)
2-Butyne
(c) 1-Butene
(d)
1-Butyne
Answer. (a)
388.
Which is the best reagent for carrying out the following
conversion?
(a)
LiAlH4
(b) Conc H2SO4
(c)
H2/Ni
(d) NaOH
Answer. (b)
389.
Which of the following reaction
mixtures will give an organic product which is ionic?
(a)
CH3CH2OH + PCl5
(b) CH3CH2OH + KBr + H2SO4
(c)
CH3CH2OH + Na
(d) CH3CH2OH + SOCl2
Answer. (c)
390. Hydroboration-oxidation of propene gives :
(a) Isopropyl alcohol
(b)
n-Propyl alcohol
(c) Isobutyl alcohol
(d) tert-Butyl alcohol
Answer. (b)
391. Hydroboration-oxidation of 2-Methylpropene gives
(a)
2-Methyl-2-propanol
(b) 1,2,3-Propanetriol
(c) 2-Methyl-1-propanol
(d)
1,2-Propanediol
Answer. (c)
392. Which of the following
compounds will not be easily oxidized?
(a)
Primary alcohol
(b) Secondary alcohol
(c) Tertiary alcohol
(d)
Aldehyde
Answer. (c)
393. Which of the following
is most resistant to oxidation?
(a) CH3CH2OH
(b) (CH3)2CHOH
(c)
HOCH2CH2OH
(d) (CH3)3COH
Answer. (d)
394. Oxidation of a primary
alcohol with produces
(a) a carboxylic acid
(b)
an ether
(c)
a ketone
(d) an ester
Answer. (a)
395. Oxidation of a secondary
alcohol with K2Cr2O7/H+ produces
(a)
a carboxylic acid
(b) a ketone
(c) an aldehyde
(d)
an ester
Answer. (b)
396. Isopropyl alcohol reacts with acidic sodium dichromate to give
(a)
Acetaldehyde
(b) Acetic acid
(c)
Propionic acid
(d) Acetone
Answer. (d)
397. Isopropyl alcohol
can be converted to acetone
by treatment with
(a) HCl/ZnCl2
(b) Na2Cr2O7/H2SO4
(c)
NaOH
(d) LiAlH4
Answer. (b)
398.
Which of the bonds in Ethyl alcohol
(CH3CH2OH) will
undergo heterolytic bond fission most
readily?
(a)
O–H
(b) C–H
(c) C–O
(d)
C–C
Answer. (a)
399.
The mechanism of dehydration of an alcohol
to give an alkene involves formation of :
(a)
Carbonium ions
(b)
Carbanions
(c) Free radicals
(d)
Carbenes
Answer. (a)
400.
The mechanism of dehydration of an alcohol
to give an ether involves formation of :
(a)
Carbonium ions
(b) Carbanions
(c)
Free radicals
(d) Carbenes
Answer. (a)
401.
The acid-catalyzed dehydration
mechanism for alcohols is best described as a(n) :
(a)
E1
(b) E2
(c)
SN1
(d) SN2
Answer. (a)
402.
When ethanol is heated with concentrated H2SO4, a gas
is produced. Which of the following
compounds is formed when this gas is treated with bromine in CCl4?E2
(a)
Bromomethane
(b)
1,2-Dibromoethane
(c) Bromoethane
(d)
1,1,2,2-Tetrabromoethane
Answer. (b)
403. What is the functional group in an alcohol?
(a)
Carbon-carbon double bond
(b) NH2
(c) OH
(d)
COOH
Answer. (c)
404. What is the IUPAC name for the following
structure?
CH3CH(CH3)CH2CH(OH)CH3
(a) 4-methyl-2-pentanol
(b)
2-methyl-2-hexanol
(c) 2-methyl-4-pentanol
(d) 2-methyl-3-pentanol
Answer. (a)
405.
Explain why the water molecule has
a bent shape and a bond angle less than 109.5°.
Answer. The electron
repulsion between the two lone pairs of electrons on the
oxygen of water causes the O–H bonds to squeeze close together.
406.
Which of the following
compounds does not have
the molecular formula C6H14O?
(a)
2-hexanol
(b) 3-methyl-2-pentanol
(c)
3-methyl-3-pentanol
(d) cyclohexanol
Answer. (d)
407. Which of the following
is a secondary alcohol?
(a) 3-ethyl-2-methyl-1-pentanol
(b)
3-ethyl-2-methyl-2-heptanol
(c) 3-methyl-2-hexanol
(d) 1-hexanol
Answer. (c)
408. Which of the following
is sec-butyl alcohol?
(a) CH3CH2CH2CH2OH
(b)
CH3CH(OH)CH2CH3
(c) (CH3)2CHCH2OH
(d)
(CH3)2CHOH
Answer. (b)
409. What is the hybridization of the oxygen
atom in CH3CH2OH?
(a)
sp
(b) 4sp3
(c) sp2
(d)
sp3
Answer. (d)
410.
Where are the two lone pairs of
electrons of the oxygen atom in an alcohol molecule
located?
(a)
in two p orbitals
(b)
in two sp orbitals
(c) in two sp2 orbitals
(d) in two sp3 orbitals
Answer. (d)
411. What is the strongest
intermolecular force present in liquid
ethanol?
(a)
induced dipole-induced dipole
(b) dipole-dipole, specifically hydrogen bonding
(c) dipole-dipole, but not hydrogen
bonding
(d)
ion-dipole
Answer. (b)
412. Which of the following
is the best method for preparing CH3Br?
(a)
CH3OH
+ Br–
(b) CH3OH + HBr
(c)
CH3OH
+ Br2
(d) CH3OH + NaBr
Answer. (b)
413.
Which of the following
reagents can be used to oxidize 1° alcohols to aldehydes?
(a)
KMnO4
(b) MnO2
(c) K2Cr2O7
(d)
PCC
Answer. (d)
12.
What is the major product from the
acid-catalyzed hydration of
2-methyl-2- pentene?
(a) 2-methylpentane
(b) 2-methyl-1-pentanol
(c)
2-methyl-2-pentanol
(d)
2-methyl-3-pentanol
Answer. (c)
414.
In
cold countries ethylene
glycol is added to water in car radiators. This helps to
(a)
Reduce the viscosity
(b) Make water a better lubricant
(c)
Lower the freezing
point
(d) Lower the boiling point
Answer. (c)
415. Ethylene oxide undergoes acid-hydrolysis to form
(a) Ethylene glycol
(b)
Formic acid
(c) Ethyl alcohol
(d) Acetic acid
Answer. (a)
416. Ethylene glycol undergoes oxidation
with hot acidic
KMnO4 to form :
(a) Formic acid
(b)
Formaldehyde
(c)
Acetic acid
(d) Acetaldehyde
Answer. (a)
417. Ethylene glycol reacts with excess of PCl5 to give
(a)
Chloroethane
(b) 1,2-Dichloroethane
(c) Hexachloroethane
(d)
1,3-Dichloroethane
Answer. (b)
418. 1,2-Ethanediol reacts with anhydrous
zinc chloride to form
(a)
Ethylene
(b) Acetaldehyde
(c)
Acetylene
(d) Ethyl chloride
Answer. (b)
419. When ethylene
glycol is heated
with concentrated HNO3, it forms
(a) Oxalic acid
(b) Ethylene oxide
(c)
Dioxane
(d) Diethylene glycol
Answer. (a)
420. Which of the following
is used as an antifreeze?
(a) Ethylene glycol
(b)
Glycerol
(c) Diethyl ether
(d) Picric acid
Answer. (a)
421. When glycerol
is heated with oxalic acid at 260°C, it gives
(a)
1,2-Propanediol
(b) Vinyl alcohol
(c) 1,3-Propanediol
(d)
Allyl alcohol
Answer. (d)
422. When glycerol
is heated with potassium hydrogen sulfate (KHSO4), it forms
(a)
Acrolein
(b) Acetic acid
(c)
Allyl alcohol
(d)
Propionic acid
Answer. (a)
423.
Glycerol on warming with a small amount of hydriodic acid gets converted to
(a)
Propene
(b) 3-Iodopropene
(c) 1,3-Diiodopropane
(d)
2-Iodopropane
Answer. (b)
424.
When glycerol is treated with a mixture of concentrated HNO3 + H2SO4, it forms
(a)
Nitroethane
(b)
1-Nitropropane
(c) Nitroglycerine
(d) 2-Nitropropane
Answer. (c)
425. In the manufacture of dynamite, one of the chemicals used is
(a)
Glycerol
(b) Glycerol triacetate
(c) Glycerol trinitrate
(d)
Glycerol triiodide
Answer. (c)
426. Which of the following
compounds is least soluble in water?
(a)
Glycerol
(b) Ethyl alcohol
(c)
Ethylene glycol
(d) Ethyl chloride
Answer. (d)
427.
Compound (A) reacts with sodium metal to form one mole of H2. The compound (A) can be
(a)
CH3CH2CH=CH2
(b) HOCH2CH2CH2CH2OH
(c) CH=CH–CH=CH2
(d)
CH3CH2CH2CH2OH
Answer. (b)
428. Ethers are
(a)
Lewis acids
(b)
Neutral
(c) Lewis bases
(d)
Can not be predicted
Answer. (c)
429. Ethanol is isomeric with
(a) Dimethyl ether
(b) Ethanal
(c)
Diethyl ether
(d) Propanone
Answer. (a)
430. Diethyl ether and methyl propyl ether are
(a) Conformational isomers
(b)
Metamers
(c) Geometrical isomers
(d) Enantiomers
Answer. (b)
431. The reaction
of a sodium alkoxide with an alkyl halide is called
(a) Wurtz-Fittig reaction
(b)
Perkin reaction
(c) Williamson's synthesis
(d)
Aldol condensation
Answer. (c)
432. Ethyl bromide reacts with sodium
methoxide to form
(a)
Diethyl ether
(b) Ethyl methyl ether
(c) Dimethyl ether
(d)
n-Propyl alcohol
Answer. (b)
433. Ethyl alcohol reacts with concentrated H2SO4 at 140°C
to form
(a) Acetone
(b) Ethylene
(c)
Diethyl ether
(d) Acetic acid
Answer. (c)
434. Ethers are kept in brown bottles
because
(a) Brown bottles
are cheaper than colorless clear bottles
(b)
Ethers absorb moisture
(c)
Ethers evaporate readily
(d) Ethers are oxidized to explosive peroxides
Answer. (d)
435.
Ethers are stored in brown bottles.
This is because on exposure
to air and light ethers are converted to
(a)
Peroxides
(b) Oxonium ions
(c)
Ozonides
(d) Electrophiles
Answer. (a)
436. Ethers can be freed from peroxides by treatment with
(a) Ferrous salt
(b)
Sodium carbonate
(c) Ferric salt
(d) Sodium bicarbonate
Answer. (c)
437. Which of the
following statements is false?
(a)
Diethyl ether has been used as a general
anesthetic
(b) Ethyl alcohol is present
in all alcoholic beverages
(c) Methyl alcohol is produced
by fermentation of sugars
(d)
Ethylene glycol is a common
antifreeze for automobiles
Answer. (c)
438. Ethers react with cold concentrated H2SO4 to form
(a)
Oxonium salts
(b) Alkenes
(c) Alkoxides
(d)
Zwitterions
Answer. (a)
439. Which of the following
reagents readily react with ethyl methyl ether?
(a) NaOH
(b) Conc HI
(c)
KMnO4
(d) H2O
Answer. (b)
440. Diethyl ether reacts with sodium metal
to give
(a) Ethanol
(b)
Sodium ethoxide
(c)
Ethanal
(d) Nothing happens
Answer. (d)
441. Diethyl ether on heating
with excess concentrated HI gives
(a)
Methyl iodide
(b) Isopropyl iodide
(c) Ethyl iodide
(d)
n-Propyl iodide
Answer. (c)
442. Diethyl ether reacts with excess of hot concentrated HI to form
(a)
CH3CH2I + CH3CH2OH
(b) Only CH3CH2OH
(c)
CH3CH2OH + CH2=CH2
(d) Only CH3CH2I
Answer. (d)
443. Which is the best reagent to accomplish the following conversion?
CH3CH2OCH2CH3 CH3CH2Br
(a)
Br2 in CCl4
(b) NaBr
(c) Br2 in H2O
(d)
Conc HBr
Answer. (d)
444.
Which of the following pairs of compounds will not form hydrogen bonds with each other?
(a)
CH3OH and CH3CH2OH
(b)
CH3SH and CH3CH2SH
(c) CH3OCH3 and CH3CH2OCH2CH3
(d) CH3COOH and H2O
Answer. (c)
445. The compound
with the lowest boiling point
is
(a)
H2O
(b) CH3CH2OH
(c) CH3OCH3
(d)
CH3CH2CH3
Answer. (d)
446. Which of the following
would have the highest boiling
point?
(a)
1-Butanol
(b)
Butane
(c) 1-Butene
(d)
1-Butyne
Answer.
(a). Alcohols
of the same chain length as alkanes, alkenes, and alkynes
have higher boiling points due to their ability to hydrogen bond.
447. Which of the following
would have the highest boiling
point?
(a) Dimethyl ether
(b)
Diethyl ether
(c) Ethyl methyl ether
(d)
Diisopropyl ether
Answer. (d). Ethers follow the same trend as alkanes, so diisopropyl ether will
have the highest boiling point because it has the highest molecular weight.
448.
Which of the following
functional group series is ranked according to increasing boiling points?
(a)
diethyl ether, ethane,
ethanol, ethanethiol
(b) ethane, ethanol,
diethyl ether, ethanethiol
(c) ethane, diethyl
ether, ethanethiol, ethanol
(d)
diethyl ether, ethane,
ethanethiol, ethanol
Answer. (c)
449.
The following compounds have identical
molecular weights. Which would have the lowest boiling point?
(a)
1-Methoxypropane
(b)
1-Butanol
(c) 1,1-Dimethylethanol
(d) 2-Butanol
Answer. (a)
450. Cyclic ethers with three-membered ring are called
(a) Lactones
(b)
Oxiranes
(c) Alkoxides
(d)
Epoxy resins
Answer. (b)
451.
Ethylene reacts with oxygen
in the presence of silver catalyst at 300°C to form
(a)
Diethyl ether
(b)
Ethylene glycol
(c) Ethyl alcohol
(d)
Ethylene oxide
Answer. (d)
452. Ethylene oxide reacts with HBr to give
(a) 1-Bromoethanol
(b)
Ethyl bromide
(c) 2-Bromoethanol
(c) Ethylene glycol
Answer. (c)
453. Acid-catalyzed hydrolysis of ethylene oxide yields
(a) CH3CH2OH
(b)
HOCH2CH2OH
(c) CH3CH2CH2OH
(d)
HOCH2CH2CH2OH
Answer. (b)
454. The product
of the reaction of ethylene
oxide with acidic methanol is
(a)
CH3OCH2CH2OH
(b) CH3CH2CH2CH2OH
(c) HOCH2CH2OH
(d)
CH3CH2OCH2CH3
Answer. (a)
455. Ethylene oxide reacts with ammonia to give
(a) 1-Aminoethanol
(b) Ethylamine
(c)
2-Aminoethanol
(d) Acetamide
Answer. (c)
456. Which of the following
is closest to the C–O–C bond angle in CH3–O–CH3?
(a) 180°
(b)
120°
(c) 109.5°
(d) 90°
Answer. (c)
457.
When dipentyl ether is treated with excess HI, through what type of mechanism(s) does the major product
result?
(a)
SN2
(b) SN1
(c)
E1
(d)
E2
Answer. (a)
458. Which of the following
is not a property
of thiols (RSH)?
(a) They are all solids
(b)
They can be oxidized to disulfides
(c) They have foul odors
(d) They are weak acids
Answer. (a)
459.
Thiols are alcohol analogs in which
the oxygen has been replaced by sulfur (e.g., CH3SH). Given the fact
that the S–H bond is less polar than the O–H bond, which of the following
statements comparing thiols and alcohols is correct?
(a)
Hydrogen bonding forces are weaker in thiols.
(b) Hydrogen bonding
forces are stronger
in thiols.
(c)
Hydrogen bonding forces would be the same.
(d) No comparison can be made without additional information.
Answer. (a)
460. Which of the following
has the lowest boiling point?
(a) CH3CH2OH
(b) CH3CH2CH2SH
(c)
HOCH2CH2OH
(d) CH3CH2CH2OH
Answer. (b)
461. Which of the following
is least soluble in water?
(a) CH3OH
(b)
CH3CH2OH
(c) CH3SH
(d) HOCH2CH2OH
Answer. (c)
462. n-Butyl bromide reacts with NaSH to give
(a)
CH3CH2CH2SH
(b) CH3SCH3
(c) CH3CH2CH2CH2SH
(d)
CH3CH2SCH2CH3
Answer. (c)
463. The carbon atom of a carbonyl
group is
(a)
sp hybridized
(b) sp2 hybridized
(c)
sp3 hybridized
(d) None of these
Answer. (b). Whenever carbon
is bonded to three other atoms or groups, it uses
sp2 hybrid orbitals
to form its bonds.
464. Which statement
about the carbonyl
group is NOT true?
(a) The carbonyl
carbon is sp2 hybridized.
(b)
The bond angles among the
three atoms attached
to the carbonyl carbon are 120°.
(c)
The three atoms
attached to the carbonyl carbon form a nonplanar
geometry.
(d)
The carbonyl group forms resonance
structures.
Answer. (c)
465. Acetone contains
(a)
nine σ bonds plus one π bond
(b) ten σ bonds
(c) eight σ bonds plus two π bonds
(d)
nine π bonds plus one σ bond
Answer. (a)
466. Formalin is
(a) 10% solution
of formaldehyde in water
(b) 20% solution
of formaldehyde in water
(c)
40% solution of formaldehyde in water
(d) 80% solution
of formaldehyde in water
Answer. (c)
467. Which of the following
will have the highest boiling
point?
(a) Propanone
(b) 2-Pentanone
(c)
Butanone
(d) 2-Hexanone
Answer. (d). Boiling points increase with molecular weight. The higher the
molecular weight, the higher is the boiling point. All of the given compounds
are ketones. 2-Hexanone has the highest molecular weight.
468. Which of the following
will have the highest boiling
point?
(a)
Methanal
(b) Ethanal
(c) Propanal
(d)
Butanal
Answer. (d). The boiling points increase
with molecular weight.
All of the given
compounds are aldehydes. Butanal
has the highest molecular weight.
469.
What property of low-molecular
weight aldehydes and ketones accounts for the magnitude of their boiling
points?
(a)
The ability to form strong
H-bonds between their molecules.
(b)
The ability of the carbonyl oxygen
to form H-bonds
with other carbonyl groups.
(c)
The ability of the polar carbonyl group to attract
other polar molecules.
(d)
The ability of the carbonyl
group to attract electrophiles and form bonds.
Answer. (c)
470.
Primary alcohols have boiling points that are the corresponding aldehydes.
(a)
Lower than
(b)
Higher than
(c) About the same
Answer. (b). For compounds of similar molecular weights, boiling points increase with the degree of
hydrogen bonding. Remember : Alcohols
form strong hydrogen bonds and will
boil at a higher temperature than the corresponding aldehydes.
471. The melting
points of aldehydes and ketones tend to :
(a)
decrease with increasing molecular weight.
(b) increase with increasing molecular weight.
(c) remain unchanged
with increasing molecular weight.
(d)
be unpredictable due to resonance.
Answer. (b)
472.
Which action best accounts
for the solubility of aldehydes
and ketones in water?
(a)
Polar interactions between solute molecules.
(b)
H-bonding between solute molecules.
(c) Van der waals forces
(d) H-bonding between
solute and solvent molecules
Answer. (d)
473. Ketones are prepared by the oxidation
of
(a)
Primary alcohol
(b) Secondary alcohol
(c) Tertiary alcohol
(d)
None of these
Answer. (b)
474. Which of the following do you consider
to be suitable for obtaining
acetone
(CH3COCH3)?
(a) Heating CH3CH2CH2OH with acidic Na2Cr2O7
(b)
Passing over heated copper
(c) Oxidation of CH3CH2CH3
with concentrated HNO3
(d)
Heating CH3CH=CH2 with
dilute H2SO4
Answer. (b)
475. Cyclopentanol
undergoes oxidation to give :
(a) Cyclopentene
(b) Cyclopentanone
(c)
Cyclopentane
(d) Cyclopentanal
Answer. (b)
476. Which statement
about the carbonyl
group of ketones
and aldehydes is true?
I.
It can attract
nucleophiles.
II.
It can attract
electrophiles.
III.
It tends to undergo addition
reactions.
IV. It tends to undergo
substitution reactions.
(a) I and III
(b)
II and IV
(c)
I, II, and III
(d) I, III, and IV
Answer. (c)
477.
Which of the following compounds reacts with sodium bisulfite and ammoniacal silver nitrate solution?
(a)
(b)
(c)
(d)
Answer. (b)
478. Acetone reacts with HCN to form
a cyanohydrin. It is an example of
(a) Electrophilic addition
(b)
Electrophilic substitution
(c) Nucleophilic addition
(d)
Nucleophilic substitution
Answer. (c)
479.
Which of the following reagents will react readily with both aldehydes and ketones?
(a)
Grignard reagent
(b) Fehling's reagent
(c) Tollens' reagent
(d)
Schiff's reagent
Answer. (a)
480.
Boiling acetaldehyde (CH3CHO) reacts
with chlorine gas to give (a)
(b)
(c)
CH3CHCl2
(d)
CHCl3
Answer. (b)
481.
The reaction of ethanal
with one equivalent of methanol and a trace of an acid will give
(a)
Acetal
(b) Hemiacetal
(c)
Ketal
(d) Hemiketal
Answer. (b)
482.
Acetone undergoes reduction with hydrazine in the presence
of NaOH to form propane. This reaction is known as
(a)
Clemmensen reduction
(b) Wolf-Kishner reduction
(c) Rosenmund reduction
(d)
Reformatsky reaction
Answer. (b)
483. Acetone undergoes reduction with zinc amalgam in HCl to form propane.
This reaction
is known as
(a) Clemmensen reduction
(b)
Wolf-Kishner reduction
(c) Rosenmund reduction
(d)
Aldol condensation
Answer. (a)
484. Cannizzaro reaction
is not given by
(a) Formaldehyde
(b)
Trimethylacetaldehyde
(c) Acetaldehyde
(d) Benzaldehyde
Answer. (c)
485. When formaldehyde is treated with 50% NaOH solution, it undergoes
(a) Cannizzaro reaction
(b)
Wurtz reaction
(c) Aldol condensation
(d)
Hydrolysis
Answer. (a)
486. The reduction
of a ketone
(a)
always gives a primary alcohol
(b) always gives a secondary
alcohol
(c) always gives a carboxylic acid
(d)
always gives a ketal
Answer. (b)
487. Reduction of acetaldehyde with H2/Ni gives
(a) Ethyl alcohol
(b) Acetic acid
(c)
Ethylene
(d) Ethane
Answer. (a)
488.
On
reduction with LiAlH4,
which of the following compounds could yield an optically active compound?
(a)
Propanal
(b) Propanone
(c) Butanal
(d)
Butanone
Answer. (d)
489. The reduction
of cyclohexanone with LiAlH4 (or NaBH4) will give
(a)
an alcohol
(b) an organic
acid
(c)
an aldehyde
(d)
a hemiketal
Answer. (a)
490. Aldehydes undergo
oxidation with KMnO4/H+ to give
(a) Alcohols
(b)
Acetals
(c) Ketones
(d) Acids
Answer. (d)
491. Oxidation of acetaldehyde with Na2Cr2O7/H+ gives
(a) Ethylene glycol
(b)
Acetic acid
(c) Ethanol
(d)
Acetone
Answer. (b)
492. A hydrazone will result from
the reaction of hydrazine with
(a)
a phenol
(b) an aldehyde
(c) an alcohol
(d)
an acid
Answer. (b)
493. Aldehydes can be
distinguished from ketones
by using
(a) Ammoniacal AgNO3 solution
(b) Phenylhydrazine
(c)
Saturated NaHSO3 solution
(d) Thionyl chloride
Answer. (a)
494. The appearance
of a silver mirror in Tollens' test indicates the presence of :
(a) an aldehyde
(b)
a ketone
(c) an alcohol
(d) an alkene
Answer. (a)
495. Acetaldehyde on treatment with Tollens' reagent gives a precipitate of
(a) Ag
(b)
AgNO3
(c) Cu2O
(d)
None of these
Answer. (a)
496.
Which of the following
compounds will give a positive
test with Fehling's solution?
(a)
Formaldehyde
(b)
Acetone
(c) Ethyl acetate
(d) Acetic acid
Answer. (a)
497. Acetaldehyde on treatment with Fehling's solution
gives a precipitate of
(a)
Cu
(b) Cu2O
(c) CuO
(d)
None of these
Answer. (b)
498.
Which of the following
will react with Fehling's solution
giving a red precipitate?
(a)
CH3CH2CHO
(b)
CH3CH2OCH2CH3
(c) CH3CH2CH2OH
(d)
Answer. (a)
499. Which of the following
compounds will give an iodoform
test?
(a)
Benzoic acid
(b) Ethanol
(c) Benzyl chloride
(d)
Methanol
Answer. (b)
500. Which of the following
compounds does not give a positive iodoform
test :
(a) Ethanol
(b) Ethanal
(c)
Methanol
(d) Propanone
Answer. (c)
501.
Which of the following compounds
does not give iodoform test on
treatment with
I2/NaOH?
(a)
Ethanol
(b) Propanone
(c)
2-Propanol
(d) Butanone
Answer. (d)
502. Which of the following
compounds will give a positive iodoform test?
(a) Benzaldehyde
(b)
2-Pentanone
(c) 3-Hexanone
(d) 3-Pentanone
Answer. (b)
503.
An
organic compound (A), C3H8O, on oxidation gives (B), C3H6O. The compound
(A) could be
(a)
an aldehyde
(b) a ketone
(c)
an alcohol
(d) an ester
Answer. (c)
504.
An
organic compound (A), C3H8O, on oxidation gives (B), C3H6O. The compound
(B) could be
(a)
a carbonyl compound
(b) an alcohol
(c) a carboxylic acid
(d)
an ether
Answer. (a)
505.
An unknown compound gave a positive
Tollens' test. Treatment of the unknown with I2/NaOH
gave a solid which was identified as iodoform. The unknown was?
(a)
Ethanal
(b)
Acetone
(c) Propanal
(d) Acetophenone
Answer. (a)
506. A compound (A) gave a positive iodoform test, but did not reduce silver nitrate in ammonia solution. Compound (A) could be
507. Which of the following
characterizes the reactions
of aldehydes and ketones?
(a)
electrophilic addition
(b) electrophilic substitution
(c) nucleophilic acyl substitution
(d)
nucleophilic addition; free radical addition
Answer. (d)
508.
Why do aldehydes undergo
nucleophilic addition reactions
while esters undergo
nucleophilic acyl substitution reactions?
(a)
The carbonyl carbon of an ester is more electrophilic than that of an aldehyde.
(b)
Aldehydes are more sterically hindered
than esters.
(c)
Once the nucleophile adds to
an aldehyde, the tetrahedral intermediate is too sterically
hindered to eliminate one of the attached groups.
(d)
Once the nucleophile adds to an aldehyde, neither
H− nor R− can be eliminated since they are strongly
basic.
Answer. (d)
509.
Which of the following reagents can
be used to reduce acetaldehyde to ethyl alcohol?
(a)
1. LiAlH4 / 2. H3O+
(b) 1. NaBH4 / 2. H3O+
(c)
H2/Pt
(d) All of these
Answer. (d)
510. What is the hybridization of the carbonyl
oxygen in carboxylic acids?
(a) sp
(b) sp2
(c)
sp3
(d) s-sp2
Answer. (b)
511.
What is the hybridization and
geometry of the carbonyl carbon in carboxylic acids and their derivatives?
(a)
sp3, tetrahedral
(b) sp2, trigonal
planar
(c)
sp2, tetrahedral
(d) sp3, trigonal
planar
Answer. (b)
512.
Organic compound (A), C4H8O, does not react with sodium or PCl5. However, it reduces an alkaline solution of a copper (II) salt on heating.
Compound (A) could be
(a) an aldehyde
(b) a primary
alcohol
(c)
a ketone
(d) a secondary
alcohol
Answer. (a)
513. Check the incorrect statement :
(a) Acetic acid is present in sour milk
(b)
Formic acid is present in insect bites
(c) Tartaric acid is present in grapes
(d) Citric acid is a tricarboxylic acid
Answer. (a)
514. In the conversion of wine to vinegar
(a) Ethanol is oxidized to acetic
acid
(b)
Ethanol is reduced to acetic acid
(c) Methanol is oxidized to acetic acid
(d)
Methanol is reduced
to acetic acid
Answer. (a)
515. Vinegar is a
(a)
5% solution of acetic acid in water
(b) 25% solution
of acetic acid in water
(c) 50% solution
of acetic acid in water
(d)
40% solution of formic acid in water
Answer. (a)
516. In succinic
acid, HOOC(CH2)nCOOH, n is equal to
(a) 1
(b) 2
(c) 3
(d) 4
Answer. (b)
517. In adipic acid, HOOC(CH2)nCOOH, n is equal to
(a) 1
(b) 2
(c) 3
(d) 4
Answer. (d)
518. The compound
in which hydrogen
bonding is not possible is
(a) CH3OCH3
(b)
H2O
(c) CH3CH2OH
(d)
CH3COOH
Answer. (a)
519. Which compound
has the highest boiling point?
(a)
CH3CH3
(b) CH3OCH3
(c) CH3CH2OH
(d)
CH3COOH
Answer. (d)
520.
When carboxylic acids and dicarboxylic acids have similar
molecular weights, how do their melting points compare?
(a)
Carboxylic acids have greater melting
points.
(b)
Dicarboxylic acids have greater melting
points.
(c) Both acids have similar melting points.
(d) No consistent trend exists.
Answer. (b)
521.
The greater acidity of carboxylic acids compared to alcohols arises primarily from
:
(a)
the electron-donating effect
of the hydroxyl group
(b) the electron-withdrawing effect of the carboxyl oxygen
(c)
the acidity of α-hydrogens of carboxylic acids
(d) the resonance
stability associated with the carboxylate ion
Answer. (d)
522.
Which of the following statements is false about
the acid-strength of acetic acid?
(a)
Acetic acid is a stronger
acid than monochloroacetic acid.
(b)
Acetic acid is a stronger
acid than propionic acid.
(c) Acetic acid is a weaker acid than trichloroacetic acid.
(d)
Acetic acid is a weaker acid than formic acid.
Answer. (a)
523.
Arrange the following compounds in order of decreasing acidity
:
(a)
(1) > (2) > (3)
(b)
(3) > (2) > (1)
(c) (3) > (1) > (2)
(d) (2) > (1) > (3)
Answer. (b)
524. Which of the following
is the strongest acid?
(a)
Formic acid
(b) Trichloroacetic acid
(c) Acetic acid
(d)
Trifluoroacetic acid
Answer. (d)
525. Which of the following
is the strongest acid?
(a)
Butanoic acid
(b) 2-Chlorobutanoic acid
(c)
3-Chlorobutanoic acid
(d) 4-Chlorobutanoic acid
Answer. (b)
526. Which of the following
is the strongest acid in aqueous solution?
(a) CH3COOH
(b) ClCH2COOH
(c)
CH3CH2COOH
(d) Cl2CHCOOH
Answer. (d)
527. Which is the strongest acid?
(a) CH3COOH
(b)
Cl2CHCOOH
(c) ClCH2COOH
(d) Cl3CCOOH
Answer. (d)
528. Which of the following compounds is most acidic?
(a) CH3COOH
(b)
ClCH2COOH
(c) CH3CH2COOH
(d)
FCH2COOH
Answer. (d)
529. Which of the following compounds is the strongest acid?
(a)
CH3COOH
(b) CH3CH2COOH
(c) CF3COOH
(d)
CH3CH2CH2COOH
Answer. (c)
530. Which of the following
compounds is least acidic?
(a) CH3CH2COOH
(b) BrCH2CH2COOH
(c)
(d)
Answer. (a)
531. Which of the following compounds is most acidic?
(a)
CH3CH2COOH
(b) BrCH2CH2COOH
(c)
(d)
Answer. (d)
532. Which of the following
will give acetic acid on acid-hydrolysis?
(a) Ethyl acetate
(b)
Acetone
(c) Methyl propionate
(d) Lactic acid
Answer. (a)
533. Propanenitrile undergoes
acid-hydrolysis to give
(a) Formic acid
(b)
Propionic acid
(c) Acetic acid
(d)
Butyric acid
Answer. (b)
534. The characteristic reaction of carboxylic acids is :
(a) electrophilic addition
(b) electrophilic substitution
(c)
nucleophilic addition
(d) nucleophilic substitution
Answer. (d)
535.
Which of the following compounds will react with Tollens' reagent to give
metallic silver?
(a)
Formic acid
(b) Ethyl alcohol
(c) Acetic acid
(d)
Acetone
Answer. (a)
536.
Which of the following compounds on
treatment with NaHCO3 will
liberate CO2?
(a)
Acetic acid
(b)
Ethylamine
(c) Acetone
(d) Ethyl alcohol
Answer. (a)
537.
Which of the following reagents will convert acetic acid into acetyl
chloride?
(a)
NaCl
(b) HCl/ZnCl2
(c)
SOCl2
(d) HCl
Answer. (c)
538. Butyric acid reacts with PCl5 to give
(a) Benzoyl chloride
(b)
1-Chlorobutane
(c) Butyryl chloride
(d) 1-Chloropropane
Answer. (c)
539. Acetic acid undergoes reduction
with LiAlH4 to give
(a) Ethanol
(b)
Ethane
(c) Ethanal
(d)
Ethyne
Answer. (a)
540.
Acetic acid reacts with
methyl alcohol in the
presence of an acid catalyst
to give
(a)
Methyl formate
(b)
Ethyl formate
(c) Methyl acetate
(d) Ethyl acetate
Answer. (c)
541. Calcium acetate
on strong heating
gives
(a) Methane + CaCO3
(b)
Ethane + CaCO3
(c) Acetone + CaCO3
(d)
Ethane + CaO
Answer. (c)
542.
CH3(CH2)4 is the sodium salt of hexanoic
acid. The water solubility of this salt is :
(a)
higher than that of hexanoic
acid
(b)
lower than that of hexanoic acid
(c) completely insoluble
(d) not predictable
Answer. (a)
543. Which of the following
compounds has the lowest boiling
point?
(a)
1-butanol
(b) butanoic acid
(c) butanenitrile
(d)
methyl propanoate
Answer. (c)
544.
Which of the following is the correct ranking in decreasing order of relative Boiling Point of carbonyl
containing compounds?
(a) primary amide > carboxylic
acid >> ester ~ acyl chloride ~ aldehyde ~ ketone
(b)
ester > carboxylic
acid >> amide ~ acyl chloride ~ aldehyde ~ ketone
(c) aldehyde ~ ketone > carboxylic acid >> ester ~ acyl chloride
~ amide
(d)
carboxylic acid > amide >>
ester ~ acyl chloride ~ aldehyde ~ ketone
Answer. (a)
545.
Acetyl chloride undergoes nucleophilic substitution at a faster rate than
methyl acetate because .
(a)
the ester is more sterically
hindered than the acid chloride
(b) the acid chloride is more sterically hindered than the ester
(c) the methoxide
is a better leaving group than chloride
(d)
chloride is a better leaving
group than methoxide
Answer. (d)
546.
Esters and amides are most easily made by nucleophilic acyl substitution
reactions on :
(a)
acid anhydrides
(b)
carboxylates
(c) carboxylic acids
(d) acid chlorides
Answer. (d)
547.
Which of the following conditions will drive the equilibrium of the Fischer esterification towards ester formation?
(a)
addition of water
(b) removal of water as it is formed
(c)
addition of alcohol
(d) both (b) and (c)
Answer. (d)
548.
Which of the following statements
describes the first step in the mechanism of
the aldol condensation?
(a)
An alpha hydrogen
is abstracted by the base to form an enolate
anion.
(b) A nucleophilic base attacks the carbonyl carbon atom.
(c) The carbonyl
oxygen is protonated by the base ion.
(d)
The alpha hydrogen
is abstracted by an acid to the enolate anion.
Answer. (a)
549. Ammonium acetate on strong heating gives
(a) Urea
(b) Formamide
(c)
Uric acid
(d) Acetamide
Answer. (d)
550. Which reaction
does not yield an ester as one of the products?
(a)
A carboxylic acid is heated with an alcohol
(b) A Grignard
reagent is added to a carboxylic acid
(c)
An acid halide is treated
with an alcohol
(d) An alkyl halide is heated with the salt of a carboxylic acid
Answer. (b)
551.
Silver acetate reacts with Br2 to form methyl bromide,
carbon dioxide, and AgBr. This
is an example of
(a)
Wurtz reaction
(b) Etard's reaction
(c)
Hunsdiecker reaction
(d) Perkin reaction
Answer. (c)
552. Hunsdiecker reaction
is used for the preparation of
(a) Alkyl chlorides
and bromides
(b) Alkyl nitrates
and nitrites
(c)
Ketenes
(d) Alcohols
Answer. (a)
553.
A compound undergoes reduction with
LiAlH4. It also dissolves in aqueous NaOH from which it can
be recovered by addition of HCl. The compound is
(a)
a carboxylic acid
(b) an ester
(c) an acid anhydride
(d)
an alcohol
Answer. (a)
554.
Acid chlorides undergo reduction to the corresponding aldehydes on treatment with hydrogen in the presence of
Pd/BaSO4. This reaction is called :
(a)
Clemmensen reduction
(b)
Rosenmund reduction
(c) Wolf-Kishner reduction
(d)
None of these
Answer. (b)
555. Acetic anhydride
is obtained by the reaction
of :
(a)
Acetic acid and sodium
(b) Acetic acid and water
(c) Acetic acid and diethyl ether
(d)
Acetic acid and P2O5
Answer. (d)
556. Acetic anhydride
reacts with ethanal
to give
(a)
Methyl acetate
(b) Methyl propanoate
(c)
Ethyl acetate
(d) Ethyl propanoate
Answer. (c)
557. Acetamide on heating with P2O5 gives :
(a) Methylamine
(b) Ethylamine
(c)
Methyl cyanide
(d) None of these
Answer. (c)
558. Acetamide is a
much weaker base than ammonia. This is because
(a)
the electron withdrawing effect of the C=O group makes the lone pair of electrons on nitrogen atom less available
for protonation.
(b)
)
the electron withdrawing effect of the C=O group makes the lone pair of
electrons on nitrogen atom more available for protonation.
(c)
the presence of CH3 group sterically hinders
the protonation of the NH2 group.
(d)
an
H atom from the nitrogen
is less easily lost from CH3CONH2 than from
NH3.
Answer. (a)
559. Which of the following
statements is False about
acetamide?
(a) reacts with Br2/NaOH to form tertiary
amine
(b) undergoes acid-hydrolysis to form acetic acid
(c)
undergoes dehydration with P2O5
to form a nitrile
(d) is a white crystalline solid, soluble in water
Answer. (a)
560. The C—C—O bond angle in is approximately
(a) 60°
(b)
109.5°
(c) 90°
(d) 120°
Answer. (d)
561.
Consider a small aliphatic 1° amine, 1° alcohol, ester, carboxylic acid, and amide, all of similar
molecular weight. Which one is most likely
to have the
highest boiling
point?
(a) The amide
(b)
The alcohol
(c) The ester
(d)
The carboxylic acid
Answer. (a). Amides can form very
strong H-bonds because of ability of the N
to donate electrons to the carbonyl (more so than OH of a carboxylic acid)
and give the O considerable negative
charge, thereby enhancing the H-bond acceptor capability of the molecule.
Considering compounds of similar molecular weight and carbon chain structure,
the general trend is (highest to lowest boiling point) : amides, carboxylic
acids, alcohols, amines, aldehydes/ketones/esters, alkynes, alkenes, and
alkanes.
562. Which of the following acid-derivatives are most stable?
(a)
Acid chlorides
(b) Esters
(c) Amides
(d)
Anhydrides
Answer. (c). Amides are the most stable of the carboxylic acid derivatives
because they have the most stable resonance forms :
563. Which of the following
will have the highest boiling
point?
(a) Diethyl ether
(b)
n-Butane
(c) Acetamide
(d)
n-Propylamine
Answer. (c)
564. Acetamide can be converted
into methylamine by
(a)
P2O5
(b) Br2/NaOH
(c) PCl5
(d)
LiAlH4
Answer. (b)
565. Acetamide on reduction with LiAlH4 gives
(a) Acetaldehyde
(b) Ethylamine
(c)
Acetone
(d)
Methylamine
Answer. (b)
566. Amides undergo hydrolysis under acidic conditions to give
(a) Carboxylic acid and amine
(b)
Carboxylic acid and ammonium ion
(c) Carboxylate ion and ammonium ion
(d) Carboxylate ion and amine
Answer. (b)
567. By which of the following methods can CH3CONH2 be converted to CH3CN?
(a) Oxidize with Na2Cr2O7/H+
(b)
Heat with concentrated sulfuric acid
(c) Heat to 200°C
(d)
Warm with P2O5
Answer. (d)
568.
Which of the following reagents will react with acetamide to form methylamine?
(a)
LiAlH4
(b)
Br2/NaOH
(c) PCl5
(d) H2/Ni
Answer. (b)
569. Which of the following
compounds does not form a salt with dilute HCl?
(a) CH3CH2CONH2
(b)
(CH3CH2)2NH
(c) CH3CH2NH2
(d) (CH3CH2)3N
Answer. (a)
570.
Propionamide on heating with a mixture of bromine and sodium hydroxide gives
(a)
Propane
(b) Propylamine
(c)
Propanol
(d) Ethylamine
Answer. (d)
571. What happens when urea is treated with hydrazine?
(a) Biuret is formed
(b)
Semicarbazide is formed
(c)
Carbon dioxide and nitrogen is formed
(d) Acetamide is formed
Answer. (b)
572. Carbonyl chloride
reacts with ammonia to give
(a)
Urea
(b) Acetone
(c) Acetamide
(d)
Chloroform
Answer. (a)
573. Which of the
following is not a constituent of normal urine?
(a)
Albumin
(b) Urea
(c)
Sodium chloride
(d) Uric acid
Answer. (a)
574. Esters can be formed by nucleophilic substitution reactions of :
(a) carboxylic acids and alcohols ; acid-catalyzed
(b) acid chlorides
and alcohols
(c)
both of the above
(d) neither of the above
Answer. (c)
575. The conversion is called :
(a) Oxidation
(b)
Dehydration
(c) Reduction
(d)
Hydrolysis
Answer. (c)
576.
The following
reaction is called
:
(a)
Saponification
(b) Condensation
(c) Elimination
(d)
Esterification
Answer. (a)
577. Hydrolysis of an ester can be accomplished by :
(a)
base-promoted hydrolysis
(b) acid-catalyzed hydrolysis
(c)
both of the above
(d) neither of the above
Answer. (c)
578. Basic-hydrolysis of esters is called
(a) Acetylation
(b)
Acidification
(c) Esterification
(d) Saponification
Answer. (d)
579.
Base-catalyzed condensation of two
ester molecules to form an alcohol and β-keto ester is called
(a)
Claisen condensation
(b) Corey-House reaction
(c)
Aldol condensation
(d) Transesterification
Answer. (a)
580. Ethyl acetoacetate undergoes acid-hydrolysis with dilute HCl to form
(a) Acetoacetic acid
(b)
Succinic acid
(c) Acetic acid
(d) Adipic acid
Answer. (a)
581. The ethyl derivative of acetoacetic ester on basic-hydrolysis gives
(a) Acetic acid
(b)
Acetic acid and propionic acid
(c) Propionic acid
(d)
Acetic acid and n-butyric acid
Answer. (a)
582. Ethyl acetate on heating with sodium ethoxide gives
(a)
Ethyl acetoacetate
(b) Sodium acetate
(c) Ethyl alcohol
(d)
Diethyl ether
Answer. (a)
583. When ethyl acetoacetate is subjected
to ketonic hydrolysis, the ketone
obtained is
(a) Dimethyl ketone
(b)
Methyl ethyl ketone
(c) Diethyl ketone
(d)
Methyl n-propyl ketone
Answer. (c)
584. Ethyl acetoacetate reacts with phenylhydrazine to give
(a)
Antipyrine
(b) Aspirin
(c) 4-Methyl uracil
(d)
DDT
Answer. (a)
585. Keto-enol tautomerism is shown by
(a) Benzaldehyde
(b) Acetone
(c)
Benzophenone
(d) Acetic acid
Answer. (b)
586. Fatty acids are
(a) Unsaturated dicarboxylic acids
(b)
Long-chain alkanoic acids
(c) Aromatic carboxylic acids
(d) Aromatic dicarboxylic acids
Answer. (b)
587. Sodium or potassium salts of fatty acids are called
(a) Proteins
(b)
Terpenes
(c) Carbohydrates
(d)
Soaps
Answer. (d)
588. Soap is
(a)
a mixture of salts of fatty acids
(b) a salt of glycerol
(c) a mixture
of ethers
(d)
a mixture of aromatic ethers
Answer. (a)
589. A wax is
(a)
a nonpolar solid
(b) a long-chain
alcohol
(c)
a triacylglycerol
(d) none of these
Answer. (a)
590. Fats and oils are
(a) monoesters of glycerol
(b)
diesters of glycerol
(c) triesters of glycerol
(d) diesters of glycol
Answer. (c). Fats are solid triesters
of glycerol. Oils are liquid triesters of glycerol.
591. Fats differ from waxes in that fats have :
(a) More unsaturation
(b) Higher melting points
(c)
A glycerol backbone
(d) Longer fatty acids
Answer. (c)
592. Oleic acid is a fatty acid containing
(a) 12 carbons
(b)
14 carbons
(c) 16 carbons
(d) 18 carbons
Answer. (d)
593.
Both stearic acid and linoleic acid have 18 carbons. Linoleic
acid is unsaturated, while
stearic acid is saturated. The melting point of stearic acid :
(a)
is higher than linoleic acid
(b) is lower than linoleic
acid
(c)
is same as linoleic acid
(d) can not predict, insufficient information
Answer. (a)
594. Liquid oils can be converted to solid fats by
(a) Hydrogenation
(b)
Saponification
(c) Hydrolysis
(d) Oxidation of double bonds
Answer. (a)
595.
Partial hydrogenation of vegetable
oils in the presence of Ni catalyst
at 200°C gives
(a)
Vanaspati ghee
(b) Margarine
(c)
Both of these
(d) None of these
Answer. (a)
596. Alkaline hydrolysis of oils (or fats) is called :
(a) Saponification
(b)
Fermentation
(c) Diazotization
(d) Rancidification
Answer. (a)
597. Saponification of a fat
(a) always results
in the formation of insoluble
soaps
(b)
produces glycerol and soap
(c) is used in the production of detergents
(d)
is used in the production
of lactic acid
Answer. (b)
598. Which of the following
compounds will not be classified as lipids?
(a)
Fats
(b) Waxes
(c) Soaps
(d)
Oils
Answer. (b)
599. Synthetic
detergents can be represented by the following
general formula
(a)
RONa
(b) ROSO3Na
(c)
RCOONa
(d) RCOOH
Answer. (b)
600. The degree of unsaturation of a
fat can be determined by means of its
(a) Iodine number
(b) Octane number
(c)
Saponification number
(d) Melting point
Answer. (a)
601. Which of the following
statements is not true about
fatty acids?
(a) Fatty acids are carboxylic
acids with long hydrocarbon side chains.
(b)
The double bonds in unsaturated fatty acids are always conjugated.
(c)
Most naturally occurring fatty
acids contain even numbers of carbons and are
unbranched.
(d)
Fatty acids can be saturated
or unsaturated.
Answer. (b)
602.
Which of the following best
explains why the melting points of saturated fats increase with
increasing molecular weight?
(a)
decreased hydrogen bonding
(b) increased hydrogen
bonding
(c) decreased intermolecular van der Waal’s interactions
(d)
increased intermolecular van der Waal’s interactions
Answer. (d)
603. Which of the following
terms best describes
the compound below?
CH3(CH2)12CO2H
(a) a fatty acid
(b)
an oil
(c) a wax
(d) a soap
Answer. (a)
604. Which of the following
terms best describes
the compound below?
CH3(CH2)7CH=CH(CH2)7CO2H
(a)
an unsaturated fatty acid
(b) a triglyceride
(c)
a synthetic detergent
(d) a micelle
Answer. (a)
605. Which of the following
statements best describes
the structure of waxes?
(a) long-chain unsaturated carboxylic acids
(b) long-chain saturated
carboxylic acids
(c)
long-chain esters
(d) short-chain esters
Answer. (c)
606. Which of the following
terms best describes
the compound below?
CH3(CH2)26CO2CH2(CH2)32CH3
(a)
a fat
(b)
a wax
(c) a terpene
(d)
an unsaturated triglyceride
Answer. (b)
607. Which of the following statements is not true
about triacylglycerols?
(a) When solids and semisolids at room temperature, they are called fats.
(b) When liquids at room temperature, they are called oils.
(c)
When hydrolyzed, they produce glycerol and carboxylate salts.
(d)
Triacylglycerols with low melting
points are composed
of saturated fatty acids, causing them to be liquids at
room temperature.
Answer. (d)
608. Triglycerides which are solids
or semisolids at room temperature are called
.
(a) oil
(b) fat
(c)
steroid
(d) cholesterol
Answer. (b)
609. Which of the following statements is not true
about phospholipids?
(a)
They are similar to triacylglycerols except that the middle OH group of glycerol reacts with a phosphate rather
than with a fatty acid.
(b)
They constitute a major component of cell membranes.
(c) Phosphatidic acid is a phospholipid.
(d)
The C-2 carbon of glycerol
in phosphoacylglycerols has the R
configuration.
Answer. (a)
610.
The compound methylamine, H3C–NH2,
contains a C–N bond. In this bond, which of the following best describes the
charge on the nitrogen atom?
(a)
slightly positive
(b)
uncharged
(c) slightly negative
(d)
–1
Answer. (c)
611. Triethylamine [(CH3CH2)3N] is a molecule
in which the nitrogen atom is
hybridized and the CNC bond
angle is .
(a) sp2; >109.5°
(b) sp2; <109.5°
(c)
sp3; >109.5°
(d)
sp3; <109.5°
Answer. (d)
612.
The N–H bond in the ammonium ion, NH4+, is formed by the overlap of what two orbitals?
(a)
sp3–sp3
(b) sp3–sp2
(c) sp2–sp2
(d)
sp3–s
Answer. (d)
613. What is the
hybridization of the nitrogen atom
in CH3NH2?
(a) sp
(b) sp2
(c)
sp3
(d) s-sp3
Answer. (c)
614. What is the hybridization of the carbon atom in CH3NH2?
(a) 3sp3
(b)
sp
(c) sp2
(d) sp3
Answer. (d)
615. What type of intermolecular interactions does (CH3CH2)2NH undergo?
(a) induced dipole-induced dipole
(b)
dipole-dipole
(c) hydrogen bonding
(d) all of these
Answer. (d)
616.
Assuming roughly equivalent molecular
weights, which of the following
would have the highest boiling point?
(a)
a tertiary amine
(b) a quaternary ammonium salt
(c)
an alcohol
(d) an ether
Answer. (b)
617. Which of the following
statements is false about
primary amines?
(a) They can be prepared by reduction
of nitriles with LiAlH4.
(b)
They do not form salts with acids.
(c)
They react
with ice-cold nitrous acid to form nitrogen
gas.
(d) They are basic and soluble in water.
Answer. (b)
618. Which of the following
statements is false about
secondary amines?
(a)
They react with chloroform and NaOH
to form isocyanides.
(b) They can be prepared
by reduction of isocyanides.
(c) They react
with acid chlorides
to give substituted amides.
(d)
They react with ice-cold nitrous acid to give nitrosamine (yellow oil).
Answer. (a)
619. The hybridization of nitrogen in an amine is
(a)
sp
(b) sp3
(c)
sp2
(d) sp4
Answer. (b)
620. Which of the
following compounds is a secondary amine? (a)
(b)
H2NCH2CH2NH2
(c)
CH3CH2NHCH3
(d)
(CH3)3N
Answer. (c)
621.
A
sample of pure amine molecules is found to possess no intermolecular H- bonding. This sample is most likely :
(a)
1° amine
(b) 2° amine
(c)
3° amine
(d) all of these
Answer. (c)
622. Which of the following
is least soluble
in water?
(a) Methylamine
(b)
Trimethylamine
(c) Dimethylamine
(d) Aniline
Answer. (d)
623. Which of the following
is most soluble in water?
(a) CH3CH2CH3
(b)
(c)
CH3CH2CH2Cl
(d) CH3CH2CH2NH2
Answer. (d)
624. Which amine is NOT soluble in water?
(a) Methylamine
(b)
Dimethylamine
(c) Trimethylamine
(d) All are water-soluble
Answer. (d). Amines from H-bonds with water. Therefore, all low-molecular weight amines are soluble in water.
625.
Consider a 1°, 2° and 3° amine, all of equivalent molecular weight. Which amine is most likely to have the
lowest boiling point?
(a)
1° amine
(b)
2° amine
(c) 3° amine
(d) Not enough information to determine
Answer. (c). The 3° amines do not form hydrogen bonds to one another. The 1°
and 2° amines can form hydrogen bonds to themselves and therefore have higher
boiling points than 3° amines.
626. Which of the following
will have the highest boiling
point?
(a) Methylamine
(b) Diethylamine
(c)
Ethylamine
(d) Triethylamine
Answer. (d)
627. Which compound
has the highest boiling point?
1. CH3CH2CH3 2. CH3CH2OH 3. CH3CH2NH2
(a) 1
(b) 2
(c) 3
(d) 2 and 3 have similar boiling
points
Answer. (b). Amines are fairly polar, but they boil at temperatures lower
than those of alcohols of similar
chain length and structure. Amines do have higher boiling points than alkanes
because they possess H-bond donors and acceptors.
628. Which of the
following has the highest boiling point?
(a)
CH3CH2CH2CH3
(b) CH3CH2CH2CH2Cl
(c)
CH3CH2CH2CH2NH2
(d) CH3CH2CH2CH2F
Answer. (c)
629. Amines are generally classified as
(a) Weak acids
(b)
Strong acids
(c) Weak bases
(d) Strong bases
Answer. (c)
630. Acetamide reacts with Br2/NaOH to give
(a)
Methylamine
(b) Urea
(c) Ethylamine
(d)
Acetyl bromide
Answer. (a)
631. Acetonitrile undergoes
reduction with LiAlH4 to form :
(a)
Methylamine
(b) Dimethylamine
(c)
Ethylamine
(d) Trimethylamine
Answer. (c)
632. Reduction of an imine will give an
(a) Acid
(b) Amide
(c)
Amine
(d) Alcohol
Answer. (c)
633. Which of the following
is most basic?
(a) Ammonia
(b)
Methylamine
(c) Dimethylamine
(d) Trimethylamine
Answer. (c)
634. Alkyl halides react with ammonia in the presence
of base to form :
(a)
primary amines
(b)
nitrated alkyl halides
(c) amides
(d)
quaternary ammonium salts
Answer. (a)
635.
The major product of the following
reaction is :
(a)
1° amine
(b) 2° amine
(c)
3° amines
(d) amide
Answer. (c)
636. Aliphatic primary
amines react with cold nitrous acid to form
(a) Alcohols
(b)
Diazonium salts
(c) Nitriles
(d) Nitroalkanes
Answer. (a)
637. Which type of amine produces N2 when treated with HONO?
(a) Primary
(b)
Secondary
(c) Tertiary
(d)
Quaternary
Answer. (a)
638. Methylamine reacts with nitrous acid to form
(a)
CH3CH3
(b) CH3OH
(c) CH3NO2
(d)
CH3CH2OH
Answer. (b)
639.
Which of the following
compounds react with nitrous acid to form an
alcohol?
(a)
CH3CH2NH2
(b)
(CH3CH2)2NH
(c) (CH3CH2)3N
(d)
Answer. (b)
640.
A
nitrile can be made by dehydrating an amide. However, for this reaction
to occur, the amide must be :
(a)
primary
(b) secondary
(c)
tertiary
(d) N-methylated
Answer. (a)
641. Which of the following
amines react with nitrous acid to form nitrosoamine?
(a) Ethylamine
(b)
Triethylamine
(c) Diethylamine
(d) Isopropylamine
Answer. (c)
642. Which of the following
does not react with acyl chlorides to form amides :
(a) ammonia
(b)
1° amine
(c) 2° amine
(d)
3° amine
Answer. (d)
643. Hinsberg's reagent
is
(a)
Pd + BaSO4
(b) p-Toluenesulfonic acid
(c) NH2NH2 + KOH
(d)
Benzenesulfonic acid
Answer. (d)
644.
Which of the following
compounds will dissolve
in aqueous NaOH after
undergoing reaction with Hinsberg reagent?
(a)
CH3CH2NH2
(b)
(CH3CH2)2NH
(c) (CH3CH2)3N
(d) (CH3)3N
Answer. (a)
645. Which of the following
compounds does not react with acetyl chloride?
(a)
Methylamine
(b) Dimethylamine
(c) Aniline
(d)
Trimethylamine
Answer. (d)
646. A primary
amine can be identified by using
(a)
HCl
(b) CHCl3
(c)
NaOH
(d) CHCl3 + KOH
Answer. (d)
647. Carbylamine test is given by
(a) Primary amines
(b) Secondary amines
(c)
Tertiary amines
(d) None of these
Answer. (a)
648. Which of the following
describes the side chain for Alanine?
(a) hydrogen
(b)
ethyl group
(c) methyl group
(d) isopropyl group
Answer. (c)
649. Which of the following
describes the side chain for Valine?
(a)
ethyl group
(b) hydrogen
(c) isobutyl group
(d)
isopropyl group
Answer. (d)
650. Which of the following
describes the side chain of Leucine?
(a)
ethyl group
(b) isopropyl group
(c)
sec-butyl group
(d) isobutyl group
Answer. (d)
651. Which of the following
amino acids has an aliphatic
R group?
(a) Serine
(b) Cysteine
(c)
Asparagine
(d) Leucine
Answer. (d)
652. Which of the following
amino acids has an aromatic
R group?
(a) Serine
(b)
Cysteine
(c) Asparagine
(d)
Tyrosine
Answer. (d)
653. Which of the following
amino acids has a sulfur in the R group?
(a)
Serine
(b) Cysteine
(c) Asparagine
(d)
Tyrosine
Answer. (d)
654. Which of the following
amino acids has a heterocyclic R group?
(a) Glycine
(b) Threonine
(c)
Proline
(d) Aspartic acid
Answer. (c)
655. The α-carbon of all the amino acids is a chirality center except for
.
(a)
Glycine
(b) Threonine
(c) Proline
(d)
Aspartic acid
Answer. (a)
656.
Which of the following is correct
for an amino acid solution when it is in the acidic form?
(a)
pH > pKa
(b)
pH < pKa
(c) zwitterionic
(d) pH = 7
Answer. (b)
657.
When a disulfide linkage
is formed, the compound containing this new linkage has
been .
(a)
hydrolyzed
(b) dehydrated
(c)
electrolyzed
(d)
oxidized
Answer. (d)
658. Which of the following
structures can polypeptides have?
(a) primary structure
(b)
secondary structure
(c) tertiary structure
(d) all of the these
Answer. (d)
659.
Which of the following is the first step in
the determination of the primary
structure of proteins?
(a)
determining the number
and kind of amino acids
in the peptide
(b) reducing the disulfide bridges in the protein
(c)
protecting the N-terminal of the peptide
(d) protecting the C-terminal of the peptide
Answer. (b)
660. What are enzymes?
(a) saccharides that catalyze chemical
reactions
(b)
unsaturated fats that catalyze chemical
reactions
(c) DNA molecules that catalyze chemical reactions
(d) proteins that catalyze chemical reactions
Answer. (d)
661.
Which of the following
may characterize the “secondary structure” of proteins?
(a)
conformation of the protein backbone
(b) α-Helix
(c)
parallel β-pleated sheet
(d) all of the above
Answer. (d)
662.
Which of the following is the “quaternary structure” of proteins concerned with?
(a)
sequence of amino acids in the peptide chain
(b)
description of the way the peptide
chains are arranged
with respect to each
other
(c)
location of the disulfide bridges
in the peptide chain
(d) conformation of the protein
backbone
Answer. (b)
663. Which of the following
protein structures does “denaturation” destroy?
(a)
primary and secondary
structures
(b) secondary and tertiary structures
(c)
tertiary and quaternary
structures
(d) secondary, tertiary,
and quaternary structures
Answer. (d)
664. Which of the following
are capable of denaturing proteins?
(a) organic solvents
(b)
extreme pH
(c) heat
(d) all of the these
Answer. (d)
665.
The monomeric
units that make up peptides and protein polymers are
.
(a) nucleic acids
(b) amino acids
(c)
oligosaccharides
(d) amylopectins
Answer. (b)
666. A zwitterion is
(a) an ion that is positively charged in solution
(b)
an ion that is negatively
charged in solution
(c) a compound that can ionize both as a base and an acid.
(d) a carbohydrate with an electrical charge.
Answer. (c)
667. A zwitterion has which of the following
properties
(a) no net charge
(b)
a high melting
point
(c) soluble in water
(d)
all of these
Answer. (d)
668. An aqueous solution of glycine
is neutral because of the
formation of :
(a)
Carbanion
(b) Zwitterion
(c) Carbonium ions
(d)
Free radicals
Answer. (b)
669. Which one of the following compounds form zwitterions?
(a)
carbonyl compounds
(b) amino acids
(c)
phenols
(d) heterocyclic compounds
Answer. (b)
670.
The pH at which the amino acid
shows no tendency to migrate when placed in
an electric field is known as its :
(a)
Isoelectric point
(b) Dipole moment
(c)
Iodine number
(d) Wavelength
Answer. (a)
671. The isoelectric point of a protein is
(a) the pH at which the protein molecule has no charges on its surface.
(b)
the pH at which a protein
in solution has an equal number of positive and negative charges.
(c)
the electric charge under isothermal conditions.
(b) None of these.
Answer. (b)
672.
Which of the following reactions is suitable
for the preparation of α-amino acids?
(a)
Schmidt reaction
(b)
Hofmann's degradation of amides
(c) Strecker's synthesis
(b) Reduction of nitro compounds
Answer. (c)
673. Glycine is
(a) NH2CH2COOH
(b)
NH2CH2CH2CH2CH2NH2
(c) NO2CH2CH2COOH
(b) BrCH2COOH
Answer. (a)
674. Glycine reacts with nitrous
acid to form :
(a)
Glycollic acid
(b) Diketopiperazine
(c) Methylamine
(d)
Ethyl alcohol
Answer. (a)
675. When glycine
is heated, it forms
(a)
Diketopiperazine
(b) Acrylic acid
(c)
Butyric acid
(d) Butyrlactam
Answer. (a)
676. Glycine is a unique amino
acid because it
(a) has no chiral
carbon
(b) has a sulfur containing R group
(c)
cannot form a peptide bond
(d) is an essential amino acid
Answer. (a)
677.
Which of the following
organic ions results
when glycine is treated with concentrated HCl?
(a)
(b)
(c)
(d) Answer. (a) 678.
Proteins are
(a) polyamides
(b) Polymers of ethylene
(c)
α-Aminocarboxylic
acids
(d)
Polymers of propylene
Answer. (a)
679.
The five elements present in most naturally
occurring proteins are :
(a) C, H, O, P, and S
(b)
N, C, H, O, and
I
(c)
N, S, C,
H, and O
(d) C, H, O,
S, and I
Answer. (c)
680.
The nitrogen content
of proteins can be quantitatively determined by
(a) Carius method
(b)
Kjeldahl's method
(c) Victor Meyer's
method
(d) Rast method
Answer. (b)
681.
Which of the following is the main structural feature of
proteins?
(a)
Peptide linkage
(b) Ester linkage
(c)
Ether linkage
(d)
α,β-Linkage
Answer. (a)
682.
The linear arrangement of amino acid units in proteins is called :
(a)
primary structure
(b) secondary structure
(c)
tertiary structure
(d) quaternary structure
Answer. (a)
683.
The primary structure of a protein
refers to :
(a) whether the protein is fibrous or globular
(b)
the amino acid sequence in the polypeptide chain
(c)
the orientation of the amino acid side chains in space
(d) the presence
or absence of an α-helix.
Answer. (b)
684.
The α-Helix is a common form of
(a)
Primary structure
(b)
Tertiary structure
(c) Secondary structure
(d)
None of these
Answer. (c)
685.
The α-Helix is held in a coiled conformation partially
because of :
(a)
Optical activity
(b) Hydrogen bonding
(c)
Resonance
(d)
Delocalization
Answer. (b)
686.
The double helical
structure of DNA is held together by
(a)
sulfur-sulfur linkages
(b) peptide bonding
(c)
hydrogen bonding
(d) glycosidic bonds
Answer. (c)
687.
Upon hydrolysis,
proteins give
(a) Amino acids
(b)
Hydroxy acids
(c) Fatty acids
(d)
Alcohols
Answer. (a)
688.
Complete hydrolysis of proteins produces :
(a)
Ammonia and carbon
dioxide
(b)
Urea and uric acid
(c) A mixture
of amino acids
(d)
Glycogen and a fatty acid
Answer. (c)
689.
Digestion of proteins
involves
(a)
changes in secondary
structure only
(b) cleavage of peptide linkages
(c)
removal of all carboxyl groups in the form of CO2.
(d)
removal of all NH2 groups in the form of NH3
Answer. (b)
690.
Irreversible precipitation of proteins caused
by heating is called :
(a) Polymerisation
(b)
Denaturation
(c)
Electrophoresis
(d) Inversion
Answer. (b)
691.
Precipitation or coagulation of proteins may be caused by
(a) Heat
(b)
Changes in pH
(c) Heavy metal salts
(d)
All of these
Answer. (d)
692.
Ninhydrin test is given by
(a)
Carbohydrates
(b)
Proteins
(c) Alkanes
(d)
Alkenes
Answer. (b)
693.
Which of the following tests is not used for testing proteins?
(a)
Ninhydrin test
(b) Biuret test
(c)
Xanthoproteic test
(d) Tollens' test
Answer. (d)
694.
A
protein solution on warming with concentrated HNO3 may turn yellow. This test is called :
(a) Xanthoproteic test
(b) Ninhydrin test
(c)
Biuret test
(d)
Million's test
Answer. (a)
695.
A compound gives a positive
Tollens' test but negative Ninhydrin test. It is
(a)
a protein
(b) an amino
acid
(c)
a monosaccharide
(d) pyridine
Answer. (c)
696.
Cycloalkanes have the same molecular
formula as :
(a) Alkanes
(b)
Alkenes
(c)
Alkynes
(d) Cycloalkenes
Answer. (b)
697.
Which of the following compounds
will give cyclopropane on treatment
with sodium in dry ether?
(a) 1,3-Dibromopropane
(b) 1,1-Dibromopropane
(c)
1,2-Dibromopropane
(d)
2,2-Dibromopropane
Answer. (a)
698.
Which of the following cycloalkanes is most reactive?
(a) Cyclopropane
(b)
Cyclohexane
(c)
Cyclobutane
(d) Cycloheptane
Answer. (a)
699.
Which of the following compounds
will react most readily with concentrated sulfuric acid?
(a) Ethane
(b) Cyclohexane
(c)
Propane
(d)
Cyclohexene
Answer. (d)
700.
A compound of formula C6H12 does not react with concentrated sulfuric acid.
The compound
could be
(a)
Alkane
(b)
Cycloalkane
(c) Alkene
(d)
Cycloalkene
Answer. (b)
701.
Which of the following
molecules will decolorize bromine in carbon tetrachloride
most readily?
(a) 1,2-Dimethylcyclopropane
(b)
Cyclopentane
(c)
1,2-Dimethylcyclobutane
(d) Cyclohexane
Answer. (a)
702.
Cyclopropane reacts with concentrated HBr to give.
(a) 1-Bromopropane
(b)
Bromocyclopropane
(c) 2-Bromopropane
(d)
1,2-Dibromopropane
Answer. (a)
703.
Cyclobutane reacts with hydrogen in
the presence of nickel catalyst at 200°C to give
(a) Butane
(b)
1-Butene
(c)
2-Butene
(d) None of these
Answer. (a)
704.
Cyclohexanol can be converted into cyclohexene by heating with
(a) Zn(Hg) and HCl
(b) Concentrated H2SO4
(c)
SOCl2
(d) H2 and Ni
Answer. (b)
705.
The bond angle between carbon
atoms in cyclohexane is
(a)
109°28'
(b)
60°
(c) 90°
(d)
120°
Answer. (a)
706.
Which of the cycloalkanes is not expected
to have ring strain?
(a)
Cyclopropane
(b) Cyclobutane
(c)
Cycloheptane
(d)
None of these
Answer. (c)
707.
The bond angle between carbon
atoms in cyclohexane is
(a)
60°
(b) 90°
(c)
109.5°
(d) 120°
Answer. (c)
708.
Which of the following statements is false about cyclohexane?
(a) It is a saturated
cyclic hydrocarbon
(b) All C–C–C bond angles are 109°28'
(c)
It is very unstable, strained
compound.
(d)
It
can exist in two conformations which are designated as the boat-form and the chair-form.
Answer. (c)
709.
The most stable conformation of cyclohexane is the :
(a)
Haworth form
(b) Boat form
(c)
Newman form
(d)
Chair form
Answer. (d)
710.
What percentage of cyclohexane
molecule is estimated to be in the
boat form at any given time?
(a) over 99%
(b)
between 90% and 99%
(c) approximately 50%
(d)
less than 1% Answer. (d)
711. Uriedes are
(a) Halogen derivatives of urea
(b)
Acetyl derivatives of urea
(c) Alkyl derivatives of urea
(d)
None of these
Answer. (b)
712.
Uric acid on oxidation with alkaline KMnO4 forms :
(a)
Urea
(b) Barbituric acid
(c)
Allantoin
(d)
Caffeine
Answer. (c)
713.
Diethyl malonate reacts with urea in the presence of sodium ethoxide to form
(a)
Uric acid
(b) Barbituric acid
(c)
Phenobarbital
(d) Barbital
Answer. (b)
714.
A carbohydrate composed
of three to ten sugar molecules is called a(n) :
(a) disaccharide
(b)
oligosaccharide
(c)
polysaccharide
(d) monosaccharide
Answer. (b)
715.
All chiral D-sugars
rotate plane-polarized light :
(a)
clockwise
(b)
counterclockwise
(c) +20.0°
(d) in a direction
that cannot be predicted but must be determined experimentally
Answer. (d)
716.
How many chirality centers are there in a 2-ketohexose?
(a) 2
(b) 3
(c) 4
(d) 5
Answer. (b)
717.
How many stereoisomers are possible for a 2-ketohexose?
(a) 2
(b) 4
(c) 8
(d) 16
Answer. (c)
718.
Which of the following
statements best describes
the difference between amylose and amylopectin?
(a)
Amylose is a branched
polysaccharide while amylopectin is a chain
polysaccharide.
(b)
Amylose is a straight-chain polysaccharide while amylopectin
is a
branched polysaccharide.
(c)
Amylose contains α-1,6-glycosidic linkage
which amylopectin does not contain.
(d)
Amylose is composed of thousands of D-glucose units while amylopectin
is composed of thousands of D-galactose units.
Answer. (b)
720. An aqueous solution of glucose behaves as an aldehyde because
.
(a)
it is hydrolyzed by water to the free aldehyde
(b)
it is a ketone, but is in equilibrium with the aldehyde
form
(c) glucose is actually a cyclic aldehyde
(d)
its cyclic hemiacetal, the predominant form, is in equilibrium with the free aldehyde form
Answer. (d)
720.
Which of the following statements best describes the meaning of “mutarotation”?
(a) a rapid exchange between
the α and β forms of diastereomeric sugars
(b) a rapid exchange between the D and L forms
(c)
a slow exchange
between hydrogen and deuterated hydrogen
(d)
a slow change in optical
rotation to reach an equilibrium value
Answer. (d)
721.
In solution,
glucose exists as .
(a) the open-chain form only
(b)
the cyclic
hemiacetal form only
(c) the cyclic acetal form only
(d)
an equilibrium mixture
of the open-chain form and cyclic hemiacetal forms
Answer. (d)
722.
Anomers of D-glucopyranose differ in their stereochemistry at .
(a) C1 (b) C2 (c) C3 (d) C4
Answer. (a)
723.
Which of the following statements best describes the meaning of a “glycoside”?
(a) It is the
mirror image of a sugar.
(b)
It is the hemiacetal of a sugar.
(c) It is the acetal of a sugar.
(d)
It is the enantiomer of a sugar.
Answer. (c)
724.
Which of the following would give a positive Tollen’s
test?
(a)
α-D-glucopyranose
(b) methyl β-D-glucopyranoside
(c)
sucrose
(d)
methyl α-D-ribofuranoside
Answer. (a)
725.
Which of the following is true about sucrose?
(a)
It hydrolyzes to fructose and glucose.
(b) It is a reducing
sugar.
(c)
It is a monosaccharide.
(d)
It undergoes mutarotation in water.
Answer. (a)
726.
Which term describes a
sugar where one of the OH groups has been replaced
with a hydrogen?
(a) amino sugar
(b)
imino sugar
(c) dehydroxy sugar
(d)
deoxy sugar
Answer. (d)
727.
Monosaccharides are classified according to :
(a)
the number of carbon atoms
in the molecule.
(b) whether they contain
an aldehyde or a ketone group.
(c) their
configurational relationship to glyceraldehyde.
(d)
all of the above.
Answer. (d)
728.
Which is a monosaccharide?
(a) Sucrose
(b)
Maltose
(c)
Galactose
(d) Cellulose
Answer. (c)
729.
Which is a disaccharide?
(a) Glucose
(b)
Maltose
(c) Fructose
(d)
Cellulose
Answer. (b)
730.
Which of the following is not a monosaccharide?
(a)
Ribose
(b)
Fructose
(c) Sucrose
(d)
Glucose
Answer. (c)
731.
The designation D or L before
the name of a monosaccharide
(a)
indicates the direction
of rotation of polarized light.
(b) indicates the length of the carbon
chain in the carbohydrate.
(c)
indicates the position of the OH group on the carbon next to the primary
alcohol group.
(d) indicates the position of the asymmetric
carbon atoms in the carbohydrate.
Answer. (c)
732.
The principal sugar in blood is
(a)
Fructose
(b)
Glucose
(c) Sucrose
(d)
Galactose
Answer. (b)
733.
Glucose cannot
be classified as
(a)
a hexose
(b) an oligosaccharide
(c) an aldose
(d)
a monosaccharide
Answer. (b)
734.
Which of the following statements is false about glucose?
(a) it is a reducing
sugar.
(b)
it is a disaccharide.
(c)
it has a pyranose form.
(d) it is a polyalcohol.
Answer. (b)
735.
Which of the following statements is false about α-D-glucose?
(a) it has a pyranose
ring.
(b)
it is a hemiacetal.
(c) it shows mutarotation.
(d)
it is the purest form of table sugar.
Answer. (d)
736.
α-D-Glucose is different from β-D-glucose
(a)
in the configuration at C-1
(b)
because they are mirror images of each other
(c) because they are enantiomers
(d)
because they are geometrical isomers
Answer. (a)
737.
α-D-Glucopyranose
is a(n) :
(a)
hemiacetal
(b) hemiketal
(c)
acetal
(d)
ketal
Answer. (a)
738.
The number of asymmetric carbon atoms in
the α-D-glucopyranose molecule is :
(a) 2
(b) 3
(c) 4
(d) 5
Answer. (d)
739.
Which of the following statements is false about an aldohexose?
(a)
It is a monosaccharide.
(b) It contains
a potential aldehyde
group.
(c) α-D-Glucopyranose is an aldohexose.
(d)
Fructose is an aldohexose.
Answer. (d)
740.
All of the following monosaccharides give the same osazone except
(a) Galactose
(b)
Glucose
(c)
Fructose
(d) Mannose
Answer. (a)
741.
Mutarotation is a term related
to
(a) Interconversion of anomers
(b)
Relationship of D- and L- families
(c) Hydrolysis of sucrose
(d)
Number of monsaccharides in a carbohydrate
Answer. (a)
742.
The mutarotation of glucose is characterized
by :
(a)
a change from an aldehyde
to ketone structure.
(b)
a change of specific rotation
from a (+) to a (–) value.
(c) the presence
of an intramolecular bridge structure.
(d)
the irreversible change from α-D to the β-D form.
Answer. (c)
743.
Which of the following statements is false about glyceraldehyde?
(a)
Its IUPAC name is 1,2-dihydroxypropanal
(b) It is isomeric with 1,3-dihydroxypropanone
(c)
It is optically
active
(d)
It shows mutarotation
Answer. (d)
744.
Common table sugar is
(a) Glucose
(b)
Sucrose
(c)
Fructose
(d) Maltose
Answer. (b)
745.
Which of the following carbohydrates is sweeter than sucrose?
(a) Glucose
(b)
Fructose
(c) Lactose
(d) None of these
Answer. (b)
746.
By approximately what factor is the
sweetness of saccharin greater than that of sugar?
(a) 5
(b)
50
(c)
500
(d) 1000
Answer. (c)
747.
Which of the following statements is false about sucrose?
(a)
It is also called table sugar.
(b)
It may be fermented by yeast to produce alcohol.
(c) It reduces
Fehling's solution.
(d)
It does not reduce Tollens'
reagent.
Answer. (c)
748.
The sugar that yields only glucose on hydrolysis is
(a)
Lactose
(b) Sucrose
(c)
Maltose
(d)
Fructose
Answer. (c)
749.
A reducing sugar will
(a)
react with Fehling's
test
(b) not react with Fehling's test
(c)
have fewer calories
(d)
always be a ketone
Answer. (a)
750.
Which of the following carbohydrates is not a reducing sugar?
(a) Glucose
(b)
Sucrose
(c)
Fructose
(d) Lactose
Answer. (b)
751.
Which of the following carbohydrates
will not give a red precipitate of Cu2O when heated with Benedict's
solution?
(a) Maltose
(b) Glucose
(c) Sucrose
(d)
Fructose
Answer. (c)
752.
Which of the following compounds reduces Tollens'
reagent?
(a) Glucose
(b)
Sucrose
(c)
Methanol
(d) Acetic acid
Answer. (a)
753.
The reagent that can be used to differentiate an aldose and a ketose is :
(a) Bromine water
(b)
Fehling's solution
(c) Tollens' reagent
(d)
None of these
Answer. (a)
754.
Starch
(a)
is a trisaccharide.
(b)
is also called
amylose.
(c) is also called amylopectin.
(d)
is a mixture of amylose + amylopectin.
Answer. (d)
755.
The monosaccharide obtained
by hydrolysis of starch is :
(a)
D-Glucose
(b) Maltose
(c)
D-Galactose
(d)
D-Ribose
Answer. (a)
756.
Which of the following statements is false about cellulose?
(a) It is a polymer of glucose molecules joined in β-1,4 linkages.
(b)
It is a major component
of cotton.
(c)
It is used in the manufacture of Dacron fibres.
(d) It is used in the manufacture of Rayon fibres
Answer. (c)
757.
Which of the following products
is not derived from cellulose?
(a) Rayon
(b)
Insulin
(c) Gun cotton
(d) Paper
Answer. (b)
758.
Coal-tar is the main source of :
(a)
Aromatic compounds
(b) Aliphatic compounds
(c)
Heterocyclic compounds
(d)
None of these
Answer. (a)
759.
Which of the following fractions
of coal-tar distillation contains benzene?
(a)
Light oil
(b) Middle oil
(c)
Heavy oil
(d) Anthracene oil
Answer. (a)
760.
Which of the following fractions of coal-tar distillation contains
naphthalene?
(a) Light oil
(b) Middle oil
(c)
Heavy oil
(d)
Anthracene oil
Answer. (b)
761.
What is the term used for isomers that are in rapid equilibrium?
(a)
keto-enol tautomers
(b) constitutional isomers
(c)
conformational isomers
(d)
cis-trans isomers
Answer. (a)
762.
Aromatic hydrocarbons are also called :
(a) Arenes
(b)
Huckel's compounds
(c)
Trienes
(d) Alkoxy compounds
Answer. (a)
763.
Which of the following is an
aromatic compound? (a)
(b)
(c)
(d)
Answer. (c)
764.
Which of the following compounds is not an aromatic compound?
(a)
(b)
(c)
(d)
Answer. (b)
765.
Which of the following compounds is known as aniline? (a)
(b)
(c)
(d)
Answer.
(c). (a) is Phenol, (b) is Toluene, and (d) is
Benzoic acid. 766. Which of the following structures represent m-dichlorobenzene?
(a)
(b)
(c)
(d)
Answer. (b)
767.
The best name for the
following compound is :
(a) 3-Methyl-bromobenene
(b) 3-Bromoaniline
(c)
3-Methylbromobenzene
(d)
3-Bromotoluene
Answer. (d)
768.
The correct IUPAC name for the following compound is :
(a) p-Nitrobenzene methanoic acid
(b)
o-Nitrobenzoic acid
(c)
o-Nitrobenzene methanoic acid
(d) m-Nitrobenzoic acid
Answer. (b)
769.
The correct
IUPAC name for the following compound is :
(a) 2-Chloro-5-fluoro-1-hydroxybenzene
(b)
1-Hydroxy-2-chloro-5-fluorobenzene
(c)
1-Fluoro-3-hydroxy-4-chlorobenzene
(d) None of these
Answer. (d). The name should be 2-Chloro-5-fluorophenol.
770.
The correct
IUPAC name for the following compound is :l
(a) 3-Bromo-4-ethyl-1-nitrobenzene
(b) 1-Ethyl-2-bromo-4-nitrobenzene
(c)
2-Bromo-4-nitrotoluene
(d)
3-Bromo-1-ethyl-4-nitrobenzene
Answer. (d). The numbering is done to produce the smallest total. Therefore,
number from the ethyl group toward the nitro group. List the substituents in
alphabetic order.
771.
Which of the following statements are correct concerning benzene?
(a) Benzene is a planar molecule.
(b)
The six carbon-carbon bonds have the same length.
(c) Benzene has alternating single
and double bonds.
(d)
(a) and (b)
Answer. (d)
772.
Which of the following statements is incorrect about benzene?
(a) All of the carbon atoms are sp hybridized.
(b)
It has delocalized electrons.
(c) The carbon-carbon bond lengths are all the same.
(d)
All twelve atoms lie in the same plane.
Answer. (a)
773.
Which of the following statements about benzene is
correct?
(a)
All of the carbon atoms are sp3 hybridized.
(b) It has no delocalized electrons.
(c)
The carbon-carbon bond length is longer than that of ethane.
(d)
It is a planar molecule.
Answer. (d)
774.
The delocalized π system
in benzene is formed by a cyclic overlap of 6 orbitals.
(a) s
(b) p
(c) sp
(d) sp2
Answer. (b)
775.
Aromatic molecules
contain π electrons.
(a)
no
(b) 4n + 2 (with n being
an integer)
(c)
4n + 2 (with n being 0.5)
(d)
4n (with
n
an integer)
Answer. (b)
776.
Which of the structures
below would be aromatic?
(a) I and IV
(b)
I, III, and IV
(c) III and IV
(d)
II
Answer. (c)
777.
Which of the following is aromatic?
(a)
cyclopentadienyl
cation
(b) 1,3-cyclohexadiene
(c) cyclobutenyl anion
(d)
cycloheptatrienyl
cation
Answer. (d)
778.
Which of the following
is not a correct
statement about the electrophilic
substitution mechanism of benzene?
(a) Benzene functions as a nucleophile.
(b)
Formation of a carbocation intermediate is the rate-determining step.
(c) The carbocation intermediate contains an sp3 hybridized carbon in the ring.
(d)
The addition product
is a frequently observed minor product.
Answer. (d)
779.
What purpose does FeCl3 serve in the electrophilic aromatic
substitution reaction between
chlorine and benzene?
(a)
It
serves as a radical initiator
to produce the chlorine radical
needed to propagate the chain
reaction.
(b)
It
functions by destabilizing the carbocationic intermediate and thereby increases
the rate of H+ loss.
(c)
It
serves as a Lewis base catalyst by reacting with Cl2 to generate chloride ions.
(d)
It serves as a Lewis acid catalyst
by reacting with the Cl2 and thereby activates it toward attack by benzene’s Ï€ electrons.
Answer. (d)
780.
Which of the following
is not a correct
statement concerning the Friedel-
Crafts acylation of benzene?
(a) An alkyl group substitutes for a hydrogen.
(b) The benzene
ring attacks an acylium ion.
(c)
The acylium ion is resonance
stabilized.
(d)
The acylium ion is often produced from an acyl chloride.
Answer. (a)
781.
What is the major organic product
of the reaction between benzene
and isobutyl chloride in the
presence of AlCl3?
(a) tert-butylbenzene
(b)
isobutylbenzene
(c) n-butylbenzene
(d)
chlorobenzene
Answer. (a)
782. Which of the following
statements are false about
benzene?
(a)
It is a planar molecule
with bond angles 120°.
(b) It is immiscible with water forming the lower layer.
(c)
It
can be converted into cyclohexane by hydrogenation at 200°C in the
presence of Ni catalyst.
(d)
It reacts with ethyl chloride in the presence of aluminium chloride
to form ethylbenzene.
Answer. (b)
783.
Which statement about the structure of benzene is not true?
(a) The two Kekule structures of benzene are in equilibrium.
(b)
The carbon-carbon bond lengths in benzene are greater than the
carbon-carbon double bonds in aliphatic compounds.
(c) The molecular
geometry of benzene
is best described as planar.
(d)
The stability of benzene
ring is much greater than the stability of 1,3,5- cycloheptatriene.
Answer. (a). Neither of the two Kekule structures for benzene has been
isolated. No equilibrium exists between these two structures because they are
resonance structures, differing only in the positions of electrons.
784.
The carbon atoms in a benzene ring are :
(a)
sp hybridized
(b) sp3 hybridized
(c)
sp2 hybridized
(d)
None of these
Answer. (c)
785.
Which of the following
compounds uses only sp2 hybridized carbons
for bond formation?
(a)
(b)
(c)
(d)
Answer. (b)
786. The C–C bond length
in benzene is
(a)
greater than the C–C bond length
in ethane.
(b)
shorter than the C–C bond length
in ethylene.
(c) Same as that of C–C bond length in ethylene.
(d)
intermediate between C–C bond length in ethane and C–C bond length in ethylene.
Answer. (d)
787.
Which of the following compounds is aromatic? (a)
(b)
(c)
(d)
Answer. (b). Use the concept of aromaticity and Huckel rule to arrive at the correct
answer.
788. Characteristic reactions
of aromatic hydrocarbons are initiated by
(a)
Electrophiles
(b)
Nucleophiles
(c) Free radicals
(d)
Uncharged molecules
Answer. (a)
789. Phenol on distillation with Zinc dust gives
(a)
Phenylzinc
(b) Benzene
(c)
Cyclohexanone
(d)
Benzoic acid
Answer. (b)
790.
Which of the following statements is false about toluene?
(a)
can be prepared by treating
benzene with methyl chloride
in the presence of AlCl3.
(b) is converted
to benzoic acid on refluxing with acidic KMnO4 solution.
(c) on refluxing
with concentrated H2SO4 gives a mixture
of ortho and para
toluenesulfonic acid.
(d)
can be nitrated
with concentrated nitric acid to give a mixture of
ortho and meta nitrotoluene.
Answer. (d)
791. Which of the following reagents will react with methyl group rather than the
benzene ring in methylbenzene?
(a)
Chlorine in the presence of uv light
(b) CH3Cl in the presence
of AlCl3
(c)
CH3COCl in the presence of AlCl3
(d) Hydrogen in the presence
of nickel
Answer. (a)
792.
Which of the following can be
made by the action of CH3Cl
on benzene in the presence of aluminium chloride?
(a) Ethylbenzene
(b) o-Xylene
(c)
Chlorobenzene
(d)
m-Xylene
Answer. (b)
793.
For reactions of
ethylbenzene, the ethyl group is considered :
(a)
ortho director
(b) ortho-para director
(c)
meta director
(d) ortho-meta director
Answer. (b)
794.
Toluene reacts with bromine in the presence
of uv light to give
(a) m-Bromotoluene
(b)
Benzyl bromide
(c)
o-Bromotoluene
(d) Benzoyl bromide
Answer. (b)
795.
Toluene reacts with chlorine in the presence
of AlCl3 to give
(a) o-Chlorotoluene
(b)
o- plus p-Chlorotoluene
(c) m-Chlorotoluene
(d)
o- plus m-Chlorotoluene
Answer. (b)
796. Toluene undergoes
oxidation to give
(a)
Benzyl alcohol
(b)
Quinone
(c) Benzaldehyde
(d)
Benzoic acid
Answer. (d)
797.
Ethylbenzene undergoes oxidation with acidic
potassium dichromate to give (a)
(b)
(c)
(d)
Answer. (d)
798.
Oxidation of cumene
with acidic K2Cr2O7 gives
(a)
Phenylacetic acid
(b) Benzaldehyde
(c)
Benzyl alcohol
(d)
Benzoic acid
Answer. (d)
799.
Oxidation of toluene with chromyl chloride
gives benzaldehyde. This reaction is known as
(a) Perkin reaction
(b)
Benzoin condensation
(c) Etard's reaction
(d)
Ozonolysis
Answer. (c)
800.
Oxidation of p-xylene with acidic potassium dichromate gives (a)
(b)
(c)
(d)
Answer. (a)
801. Cresols on distillation with zinc dust gives
(a)
o-Xylene
(b) Benzene
(c)
o- plus p-Xylene
(d) Toluene
Answer. (d)
802.
An organic compound (A) has a molecular weight 78 and an
empirical formula CH. (A) is
resistant to attack by oxidizing agents but undergoes substitution and addition reactions. X-ray analysis shows that the distance between adjacent carbon atoms is
1.39Ã… (intermediate between single and double bond lengths). The evidence
suggests that compound (A) is
(a) Benzene
(b) Cyclohexane
(c)
Toluene
(d)
n-Hexane
Answer. (a)
803.
Benzene undergoes substitution
reaction more easily than addition
reaction because
(a) it has a cyclic structure
(b)
it has three double bonds
(c) it has six hydrogen
atoms
(d)
there is delocalization of electrons
Answer. (d)
804.
Benzene reacts with concentrated HNO3 in the presence of concentrated
H2SO4 to give nitrobenzene. This reaction is an example
of
(a) Electrophilic addition
(b)
Nucleophilic addition
(c)
Electrophilic substitution
(d) Nucleophilic substitution
Answer. (c)
805.
Which of the following agents is used in order
to make benzene react with concentrated nitric acid to give
nitrobenzene?
(a) Concentrated H2SO4
(b) FeCl3 catalyst
(c)
Lindlar's catalyst
(d)
Ultraviolet light
Answer. (a)
806.
Which of the following agents is used in order
to make benzene react with acetyl chloride to give acetophenone?
(a) Ultraviolet light
(b)
AlCl3 catalyst
(c) Platinum catalyst
(d)
Al2O3 catalyst
Answer. (b)
807.
Which of the following agents is used in order
to make benzene react with bromine to give bromobenzene?
(a) Ultraviolet light
(b)
Fe catalyst
(c) Nickel catalyst
(d)
Al2O3 catalyst
Answer. (b)
808. In the Friedel-Craft acetylation of an aromatic
ring, the role of the AlCl3 is to
(a) Form a ion.
(b) Function as a Lewis base
(c)
Chlorinate the aromatic
ring
(d)
Withdraw electrons from the aromatic
ring
Answer. (a)
809.
The electrophile which is considered to be the active agent in the nitration of benzene is
(a)
(b)
(c)
(d)
Answer. (c)
810.
In
chlorination of benzene, FeCl3 is
used to generate (a)
(b) Cl+
(c) Cl2
(d)
HCl
Answer. (b)
811. In sulfonation of benzene, the attacking species
is
(a)
H+
(b)
SO2
(c) SO3
(d)
Answer. (c)
812.
Consider the following reaction
:
The catalyst
used to complete the above reaction is
(a)
LiAlH4
(b)
AlCl3
(c) Na
(d)
KOH
Answer. (b)
813.
Benzene reacts with H2
at 150°C at 30 atm in the presence of Ni catalyst to give
(a) Cyclohexane
(b)
Cyclohexene
(c)
n-Hexane
(d) No reaction
occurs
Answer. (a)
814.
Benzene reacts with chlorine in the presence of FeCl3 catalyst to form
(a) Hexachlorobenzene
(b)
Chlorobenzene
(c) Hexachlorocyclohexane
(d)
Benzyl chloride
Answer. (b)
815. Benzene reacts with acetic anhydride in the presence
of AlCl3 to form
(a)
Acetophenone
(b)
Benzophenone
(c) Phenylacetic acid
(d)
Phenyl acetate
Answer. (a)
816.
Benzene reacts with benzoyl chloride in the presence
of anhydrous aluminium chloride to form
(a) Benzyl chloride
(b)
Benzaldehyde
(c)
Benzal chloride
(d) Benzophenone
Answer. (d)
817.
Benzene undergoes Friedel-Crafts reaction
with isopropyl alcohol
in the presence of H2SO4 catalyst to give
(a) n-Propylbenzene
(b)
Benzophenone
(c)
Isopropylbenzene
(d) Nothing happens
Answer. (c)
818. Benzene reacts with propene in the presence of H2SO4 catalyst
to give
(a)
n-Propylbenzene
(b)
Benzophenone
(c) Cumene
(d)
Nothing happens
Answer. (c)
819. Ozonolysis of benzene gives
(a)
Formic acid
(b) Glyoxal
(c)
Formaldehyde
(d)
Glycine
Answer. (b)
820.
Gammexane is
(a)
Hexachloroethane
(b) DDT
(c)
Hexachlorocyclohexane
(d)
TNT
Answer. (c)
821.
Which group is an activating substituent?
(a) –NO3
(b)
–Cl
(c)
–OH
(d) –F
Answer. (c)
822.
Which of the following compounds reacts most rapidly
with HNO3/H2SO4?
(a) toluene
(b)
anisole
(c) nitrobenzene
(d) benzonitrile
Answer. (b)
823.
In electrophilic aromatic substitution reactions a chlorine substituent
.
(a) is a deactivator and a m-director
(b)
is a deactivator and an o,p-director
(c)
is an activator
and a m-director
(d) is an activator and an o,p-director
Answer. (b)
824.
Which of the following
substituents is an ortho and para director and ring deactivating?
(a) –NH2
(b) –Cl
(c)
–OCH3
(d)
–OH
Answer. (b)
825.
Which of the following will undergo substitution in the ortho and
para
positions rather than in the meta position?
(a)
Nitrobenzene
(b)
Benzoic acid
(c) Acetanilide
(d)
Benzaldehyde
Answer. (c)
826. Phenol is an ortho-para director because the hydroxyl
group :
(a)
donates electrons that increase
electron density at ortho and para positions favoring nucleophilic
attack.
(b)
donates electrons that increase
electron density at ortho and para positions favoring electrophilic
attack.
(c)
donates electrons to the ortho
and para positions and attracts
electrons away from meta positions favoring nucleophilic
attack of the ring.
(d)
donates electrons to the ortho
and para positions and attracts
electrons away from meta positions favoring electrophilic
attack on the ring.
Answer. (b)
827. Compared to benzene,
nitration of toluene takes place at
(a)
Same rate
(b) Faster rate
(c)
Slower rate
(d) Can not predict
Answer. (b)
828. Electron-withdrawing groups
are meta directors because :
(a)
the carbonium ion intermediate has a
negative charge on the meta position.
(b)
the more stable resonance
hybrid occurs with meta attachment of the electrophile.
(c)
the less stable resonance hybrid occurs with meta attachment of the electrophile.
(d)
the carbonium ion intermediate has a positive charge on
the meta position. Answer. (b). When the electrophile attaches to
the benzene ring, a carbonium ion is formed. This carbonium ion is relatively stable because the charge can be
delocalized about the ring. Ortho or para attack results in a resonance form, with the positive charge on the carbon bearing
the electron-withdrawing group (highly unstable). This resonance form does not occur with meta placement of the
incoming electrophile.
829.
Which compound undergoes
substitution reactions faster than benzene? (a)
(b)
(c)
(d)
Answer. (d). Remember that activating (electron-donating) groups on benzene result in enhanced electrophilic
substitution.
830.
Which compound undergoes substitution reactions slower than benzene?
(a)
(b)
(c)
(d)
Answer. (c). The halogen
(–F) is the only deactivating group because of its
electronegativity and its low resonance potential.
831. Which of the following compounds undergoes nitration
most readily?
(a)
Benzene
(b)
Toluene
(c) Nitrobenzene
(d)
Benzoic acid
Answer. (b)
832. Which of the following
compounds is most readily sulfonated?
(a)
Benzene
(b) Chlorobenzene
(c)
Toluene
(d)
Nitrobenzene
Answer. (c)
833.
p-Nitrotoluene on treatment with chlorine in the presence
of FeCl3 gives
(a)
m-Chlorotoluene
(b) 2-Chloro-4-nitrotoluene
(c)
p-Chlorotoluene
(d) 2-Nitro-4-chlorotoluene
Answer. (b)
834.
How many isomeric
dichlorobenzenes are there?
(a) 3
(b) 6
(c) 9
(d) 12
Answer. (a)
835. Which of the following compounds has maximum
dipole moment?
(a) p-Dichlorobenzene
(b)
m-Dichlorobenzene
(c) o-Dichlorobenzene
(d)
Carbon tetrachloride
Answer. (c)
836.
Which of the following reagents
is most suitable for preparing chlorobenzene
from benzene?
(a) Aqueous chlorine
(b)
Chlorine in the presence of ultraviolet
light
(c) Chlorine in acetic acid
(d)
Chlorine in the presence of FeCl3
Answer. (d)
837.
Which of the reactions between the
following pairs of reagents proceeds
by a mechanism that may be described
as an electrophilic substitution?
(a) Benzene + Br2/FeBr3
(b) Propene + Br2
(c)
Acetone + NH2NH2
(d) Ethyl bromide
+ aq KOH
Answer. (a)
838.
Aryl halides are less reactive
towards nucleophilic substitution as compared
to alkyl halides due to
(a) Inductive effect
(b) Resonance stabilization
(c)
Tautomerism
(d)
Stereoisomerism
Answer. (b)
839.
Which of the following compounds
would be unaffected by boiling aqueous NaOH?
(a) Chloroethane
(b)
Acetaldehyde
(c) Chlorobenzene
(d)
Ethyl acetate
Answer. (c)
840. Hydrolysis of benzal chloride gives
(a)
Phenol
(b)
Benzaldehyde
(c) Benzyl alcohol
(d) Benzoyl chloride
Answer. (b)
841. Hydrolysis of benzotrichloride gives
(a)
Benzophenone
(b) Benzoic acid
(c)
Benzyl alcohol
(d)
Phenol
Answer. (b)
842.
Which reagent
can be used to carry out the following conversion?
(a) HNO3 + H2SO4
(b)
NaNO2
(c)
NaNO2
- HCl at 5°C
(d) NO2
Answer. (a)
843.
The
following compound is called?
(a) Chloral
(b)
DDT
(c) Lindane
(d)
BHC
Answer. (b)
844.
DDT is prepared by the reaction
of chlorobenzene with (in the presence of conc. H2SO4)
(a) Chloral
(b)
Chlorine
(c)
Chloroform
(d) Carbon tetrachloride
Answer. (a)
845.
Which of the following reagents can be used to distinguish between chlorobenzene and allyl chloride?
(a) H2/Ni
(b) Br2 in CCl4
(c)
Zn/HCl
(d) NH2NH2
Answer. (b)
846.
Which of the following reagents can be used to distinguish between chlorobenzene and benzyl chloride?
(a) alcoholic AgNO3
(b) Br2 in CCl4
(c)
KCN
(d)
Br2 in H2O
Answer. (a)
847.
An
organic compound (A) was
heated with a solution of NaOH.
The resulting solution was cooled, acidified with dilute HNO3, and
then AgNO3 solution was added. This gave a white precipitate. The
compound (A) may be
(a)
(b)
(c)
(d)
Answer. (b)
848. Which of the following
statements is False/Incorrect about nitrobenzene?
(a)
is formed by nitration of benzene at temperatures below 60°C.
(b)
can be
further nitrated to give m-dinitrobenzene.
(c) can be oxidized with KMnO4 to give benzoic acid.
(d)
can be reduced with Sn/HCl to give aniline.
Answer. (c)
849.
Which of the following
compounds reacts least rapidly in electrophilic
substitution reactions?
(a) Nitrobenzene
(b)
Phenol
(c) Bromobenzene
(d)
Toluene
Answer. (a)
850. Nitrobenzene reacts with Br2 in the presence of FeCl3 to give
(a) o-chloronitrobenzene
(b)
o-bromonitrobenzene
(c) m-chloronitrobenzene
(d)
m-bromonitrobenzene
Answer. (d)
851.
Nitration of nitrobenzene with HNO3/H2SO4
gives :
(a)
m-dinitrobenzene
(b) o-dinitrobenzene
(c)
p-dinitrobenzene
(d)
m-nitrobenzenesulfonic acid
Answer. (a)
852.
Nitrobenzene undergoes reduction
with zinc and KOH to give
(a) Aniline
(b)
Hydrazobenzene
(c)
Azobenzene
(d) None of these
Answer. (b)
853.
Reduction of p-nitrotoluene with Sn + HCl gives :
(a) p-methylaniline
(b)
Toluene
(c) m-methylaniline
(d)
N-Methylaniline
Answer. (a)
854. Which of the following
statements is false about aniline?
(a)
It is a primary aromatic
amine.
(b)
It is a weak base which forms salts with acids.
(c) It liberates nitrogen on treatment
with ice-cold nitrous acid.
(d)
It can be prepared by the reduction
of nitrobenzene with tin and HCl.
Answer. (c)
855.
Which of the following statements is correct about aniline?
(a)
is weak acid.
(b)
diazotizes to benzenediazonium
chloride when treated with ice-cold
nitrous acid.
(c) can be nitrated with concentrated HNO3 to form p-nitroaniline.
(d) gives an intense green color with a suspension of bleaching powder in water.
Answer. (b)
856. Which of the following
statements is false about benzylamine?
(a) can be prepared by reduction of benzonitrile with LiAlH4.
(b)
cannot be prepared by reduction of benzamide with LiAlH4.
(c) reacts with nitrous acid to give benzyl alcohol.
(d)
reacts with KMnO4 to give benzoic
acid.
Answer. (b)
857.
Aniline is prepared by
(a)
the reaction of benzene with ammonia
(b) the reduction of nitrobenzene with Sn/HCl
(c)
the dehydrogenation of nitrobenzene
(d)
the reaction of nitrobenzene with I2/NaOH
Answer. (b)
858.
Benzamide reacts with Br2 and KOH to give
(a) Benzene
(b)
Benzylamine
(c)
Aniline
(d) Benzonitrile
Answer. (b)
859.
When ammonia is added to an alkyl halide, in the presence
of base :
(a) primary amines form
(b)
amides form
(c) nitrated alkyl halides form
(d)
quaternary ammonium salts form
Answer.
(a).
Salts of 1° amines can be prepared from ammonia
and alkyl halides. Treating the ammonium salt
with base gives a 1° amine.
860. Aniline reacts with bromine
water to form
(a)
Bromobenzene
(b)
m-Bromoaniline
(c) 2,4,6-Tribromoaniline
(d)
o- plus p-Bromoaniline
Answer. (c)
861.
Which of the following will give a precipitate with excess bromine
water?
(a)
Bromobenzene
(b) Aniline
(c)
Nitrobenzene
(d)
Toluene
Answer. (b)
862. Aniline reacts with nitrous acid at low temperatures to give
(a)
a N-nitrosoamine
(b) a nitrile
(c)
a diazonium salt
(d) a nitrite
salt
Answer. (c)
863.
When aniline is heated with chloroform and alcoholic KOH, the product is
(a) Benzonitrile
(b)
p-Chloroaniline
(c)
Phenylisocyanide
(d) m-Chloroaniline
Answer. (c)
864. Aniline reacts with acetic anhydride to give :
(a)
N-Methylaniline
(b)
p-Aminoacetophenone
(c) Acetanilide
(d)
m-Aminoacetophenone
Answer. (c)
865. Aniline undergoes oxidation
with Na2Cr2O7/H2SO4 to give
(a)
Schiff's base
(b) p-Benzoquinone
(c)
Phenol
(d)
Benzoic acid
Answer. (b)
866.
Which of the following reagents
does not react with aniline?
(a)
Acetyl chloride
(b) Acetic anhydride
(c)
Ammonia
(d) Nitrous acid
Answer. (c)
867.
Rank the following compounds
in order of increasing base strength :
(a) 1, 2, 3
(b)
3, 2, 1
(c)
2, 3, 1
(d)
2, 1, 3
Answer. (c). The aromatic amines are weaker bases than the nonaromatic
cyclic amines because the lone-pair electrons on nitrogen are delocalized over
the aromatic ring. This delocalization stabilizes the compound but also
decreases the ability of the nitrogen to act as a base. Compound (3) is a stronger base than aniline because of the electron-releasing substituent
on the ring.
868.
Rank the following compounds
in order of increasing base strength :
(a) 1, 2, 3, 4
(b) 4, 2, 3, 1
(c)
1, 4, 3, 2
(d)
4, 3, 1, 2
Answer. (d). Of the aromatic amines, the weakest base is the one with the electron-withdrawing substituent: (4) is
the weakest followed by aniline (3). Compound (2) is the strongest base because
its electrons are not delocalized effectively into the aromatic ring,
and it is therefore
a primary amine, and its pKa
is slightly lower than that of ammonia.
869.
Which of the following compounds
is most basic?
(a) Aniline
(b)
Benzylamine
(c)
Acetanilide
(d) p-nitroaniline
Answer. (b)
870. Which of the following
is most basic?
(a)
CH3NH2
(b)
(CH3)3N
(c) (CH3)2NH
(d)
Answer. (c)
871.
Which of the following is most basic?
(a)
(CH3)2NH
(b)
(c)
(d) NH3
Answer. (a)
872.
Which of the following compounds is most basic? (a)
(b)
(c)
(d)
Answer. (a)
873.
Which of the following is least
basic?
(a) Aniline
(b)
p-Nitroaniline
(c)
Ammonia
(d) Trimethylamine
Answer. (b)
874. Which of the following
is least basic?
(a)
CH3NH2
(b)
(CH3)3N
(c) (CH3)2NH
(d)
Answer. (d)
875.
Which of the following compounds
is least basic?
(a)
(b)
(c)
(d)
Answer. (c)
876.
Which of the following
compounds will be most soluble
in water at room
temperature?
(a) Phenol
(b)
Phenylammonium chloride
(c)
Benzoic acid
(d) Benzylamine
Answer. (b)
877.
The diazonium salts are the reaction products of the reaction of nitrous acid with
(a) primary aliphatic
amines
(b) primary aromatic
amines
(c)
secondary aliphatic amines
(d)
secondary aromatic amines
Answer. (b)
878.
Preparation of a diazonium salt from a primary aromatic
amine is known as :
(a)
Coupling reaction
(b) Sandmeyer reaction
(c)
Diazotization
(d) Corey-House synthesis
Answer. (c)
879.
Which of the following reagents is used to prepare benzenediazonium
chloride from aniline?
(a)
NaNO2
+ HCl
(b) LiAlH4
(c)
NH2NH2 + KOH
(d) NaOH
Answer. (a)
880.
Which of the following
are optimum temperature conditions for making
benzenediazonium chloride from aniline?
(a) 0°C to 10°C
(b) 20°C to 25°C
(c)
30°C to 40°C
(d)
45°C to 50°C
Answer. (a)
881.
Benzenediazonium chloride reacts with warm water to give
(a)
Aniline
(b) Phenol
(c)
Benzene
(d) Chlorobenzene
Answer. (b)
882.
Bromobenzene can be prepared by treating aniline
with
(a) Conc HBr
(b)
Br2/FeBr3
(b) CuBr
(d) Nitrous acid then CuBr
Answer. (d)
883.
Chlorobenzene can be prepared by treatment of aniline with
(a) Cuprous chloride
(b)
Chlorine in the presence of UV light
(c) Nitrous acid followed by treatment
with CuCl
(d)
Chlorine in the presence of FeCl3
Answer. (c)
884. Iodobenzene can be prepared
by
(a)
treating chlorobenzene with I2 using FeCl3 catalyst.
(b)
treating phenol with I2 in NaOH solution.
(c) treating benzenediazonium chloride with KI
(d)
treating benzene with CH3I using AlCl3 catalyst.
Answer. (c)
885. Benzenediazonium chloride
reacts with KI to form :
(a)
Benzenediazonium iodide
(b) m-Diiodobenzene
(c)
Iodobenzene
(d) o- plus p-Diiodobenzene
Answer. (c)
886.
What is the major product of the following
reaction?
(a) Benzonitrile
(b)
Benzoic acid
(c) Nitrobenzene
(d)
Benzenediazonium chloride
Answer. (a)
887.
Benzenediazonium
chloride reacts with hypophosphorus acid to
form :
(a)
Phenol
(b) Benzaldehyde
(c)
Aniline
(d)
Benzene
Answer. (d)
888.
Benzenediazonium
chloride reacts with phenol to form :
(a) p-chlorophenol
(b)
Chlorobenzene
(c)
p-Hydroxyazobenzene
(d) DDT
Answer. (c)
889.
Phenol is used
(a) in alcoholic
beverages
(b)
as anesthetic
(c) in antiseptics
(d)
as moth repellant
Answer. (c)
890. Which of the following
compounds is aspirin
(a)
Methyl salicylate
(b)
Salicylic acid
(c) Phenyl salicylate
(d) Acetylsalicylic acid
Answer. (d)
891. When phenol is treated with neutral FeCl3 solution,
it develops
(a)
Violet color
(b) Yellow color
(c)
Green color
(d)
Nothing happens
Answer. (a)
892.
Which of the following compounds
will react with PCl5 least vigorously?
(a)
Ethanol
(b) Acetic acid
(c)
Phenol
(d) Benzoic acid
Answer. (c)
893.
Sodium phenoxide reacts with CO2 at 125°C under 5 atm
pressure to give salicylic acid. This reaction is called
(a) Kolbe's reaction
(b) Perkin reaction
(c)
Wurtz reaction
(d)
HVZ reaction
Answer. (a)
894.
Phenol reacts with excess bromine water to give
(a)
o- plus p-Bromophenol
(b) Bromobenzene
(c)
2,4,6-Tribromophenol
(d)
m-Bromophenol
Answer. (c)
895.
Resorcinol on distillation with zinc dust gives
(a) Benzene
(b)
Cyclohexane
(c)
Toluene
(d) m-Xylene
Answer. (a)
896.
Bakelite has the following characteristics
(a) A polymer
made from phenol
and formaldehyde
(b)
A thermosetting plastic
(c) Can be used as an adhesive
(d) All of the above
Answer. (d)
897. Anisole is formed when phenol is treated with
(a)
CH3I/NaOH
(b) CH3CH2I/NaOH
(c)
CHCl3/NaOH
(d)
Acetic anhydride
Answer. (a)
898.
Anisole on heating
with concentrated HI gives
(a)
Iodobenzene
(b) Phenol + CH3I
(c)
Iodobenzene + CH3OH
(d) Phenol + CH3OH
Answer. (b)
899.
Which group forms the strongest H-bonds to water molecules?
(a) Alcohols
(b)
Ethers
(c)
Phenols
(d) All equally
strong
Answer. (c)
900. The compound which is most capable
of hydrogen bonding
is :
(a)
CH3OCH2CH3
(b)
CH3CH2CH2CH3
(c)
(d)
CH3CH2—S—S—CH2CH3
Answer. (c)
901.
Rank the following molecules
in decreasing order of boiling
points :
(a) (3) > (2) > (1)
(b) (2) > (3) > (1)
(c)
(3) > (1) > (2)
(d)
(2) > (1) > (3)
Answer. (a). Hydroxyl groups can more
easily form intramolecular H-bonds in the
ortho position than in the meta or para positions. These intramolecular H-bonds decrease boiling
point. Therefore, compound (3) has a higher boiling point than compound (2).
Compound (2), with two hydroxyl
groups, has a still higher boiling point than phenol.
902.
Rank the following compounds
in order of increasing boiling
point :
(a) (1) < (2) < (3)
(b) (3) < (1) < (2)
(c)
(1) < (3) < (2)
(d)
(3) < (2) < (1)
Answer. (d)
903.
Phenol is acidic because of
(a) Resonance
(b)
Electromeric effect
(c)
Inductive effect
(d) Peroxide effect
Answer. (a)
904.
Which of the following has the most acidic proton?
(a) Thiol
(b)
Alcohol
(c) Phenol
(d)
Ether Answer. (c) 905. Phenol is
(a) stronger acid than acetic
acid
(b)
weaker acid than acetic acid
(c)
stronger base
than methylamine
(d) weaker base than methylamine
Answer. (b)
906.
Which of the following compounds
is least acidic?
(a) HCl
(b)
Phenol
(c) Acetylene
(d)
Picric acid
Answer. (c)
907.
Which of the following compounds
is least acidic?
(a) Formic acid
(b)
Ethanol
(c) Acetic acid
(d)
Phenol
Answer. (b)
908. Which of the following compounds is most acidic?
(a)
Formic acid
(b)
Ethanol
(c) Acetic acid
(d)
Phenol
Answer. (a)
909.
Which of the following compounds
is most acidic?
(a)
Water
(b) Cyclohexanol
(c)
Ethanol
(d)
Phenol
Answer. (d)
910.
Which one
is most acidic?
(a) Hexanol
(b)
Phenol
(c)
Water
(d) Diisopropyl ether
Answer. (b)
911. Which of the following compounds is most acidic?
(a) o-Cresol
(b)
p-Nitrophenol
(c) p-Cresol
(d)
p-Chlorophenol
Answer. (b)
912. Which of the following compounds is most acidic?
(a)
Phenol
(b)
m-Nitrophenol
(c) m-Cresol
(d)
m-Bromophenol
Answer. (b)
913.
Which molecule
is the most acidic?
(a) (1)
(b)
(2)
(c) (3)
(d)
(2) and (3) have similar acidities
Answer. (b). Acidity is enhanced
when the conjugate base is further
stabilized. By placing an electron-withdrawing group on the ring, the phenoxide
ion is further stabilized when the charge spreads over more atoms (greater
delocalization). The methoxy group is electron-releasing and destabilizes the
phenoxide.
914.
Which of the following compounds is most acidic?
Answer. (c)
915.
Which of the following
compounds is least acidic?
Answer. (b)
916.
Arrange the following
compounds in order of increasing acidity :
(a) (1) < (3) < (2)
(b)
(1) < (2) < (3)
(c)
(3) < (2) < (1)
(d) (2) < (1) < (3)
Answer. (a)
917. Phenols can be easily distinguished from alcohols because
(a)
phenols are soluble
in NaOH, but alcohols are not
(b)
alcohols are soluble
in NaOH, but phenols are not
(c) phenols are soluble in NaHCO3, but alcohols are not
(d)
alcohols are soluble
in NaHCO3, but phenols are not
Answer. (a)
918.
Benzoyl chloride reacts with hydrogen in the presence
of palladium and barium
sulfate to give :
(a) Benzyl alcohol
(b)
Benzaldehyde
(c)
Cinnamic acid
(d) Benzophenone
Answer. (b). This is Rosenmund reduction.
919.
Cinnamaldehyde is
prepared by the treatment of :
(a) benzaldehyde with acetaldehyde in the presence
of NaOH
(b)
benzaldehyde with formaldehyde in the presence
of NaOH
(c) benzophenone with acetaldehyde in the presence
of NaOH
(d)
benzophenone with formaldehyde in the presence
of NaOH
Answer. (a)
920.
Benzaldehyde reacts with
methylmagnesium iodide (followed by
hydrolysis) to form
(a) 1-Phenylethanol
(b)
Acetophenone
(c)
2-Phenylethanol
(c) Benzophenone
Answer. (a)
921. Which of the following
will undergo Aldol condensation?
(a)
Acetone
(b) Benzaldehyde
(c)
Benzoic acid
(c) Benzophenone
Answer. (a)
922.
When benzaldehyde is heated
with concentrated NaOH, it gives :
(a) Benzyl alcohol
(b)
Sodium benzoate
(c)
Benzoic acid
(d) Benzyl alcohol + Sodium
benzoate
Answer. (d). This is Cannizzaro reaction.
923.
Benzaldehyde reacts with acetic
anhydride in the presence of sodium acetate
at 180°C to give :
(a) Mandelic acid
(b) Cinnamic acid
(c)
Malonic acid
(d) Benzoic acid
Answer. (b). This is Perkin reaction.
924.
Which of the following reagents will give an addition
reaction with benzaldehyde?
(a) NaHSO3
(b)
I2/NaOH
(c) H2SO4
(d)
Answer. (a)
925.
Benzaldehyde reacts with a mixture of concentrated sulfuric
acid and nitric acid to give
(a) p-Nitrobenzaldehyde
(b)
o-Nitrobenzaldehyde
(c) p-Nitrobenzoic acid
(d)
m-Nitrobenzaldehyde
Answer. (d)
926. Acetophenone reacts with Br2 in the presence of FeCl3 to form :
(a)
m-Bromoacetophenone
(b) m-Dibromobenzene
(c) o- + p-Bromoacetophenone
(d)
p-Dibromobenzene
Answer. (a)
927.
Which of the following statements is NOT correct
:
(a) Tollens' test is given by both aliphatic and aromatic aldehydes.
(b)
Fehling's test is given by aliphatic
aldehydes. It is not given by aromatic aldehydes.
(c) Iodoform test is given by methyl
ketones and acetaldehydes.
(d)
Lucas test is given by both aliphatic
and aromatic aldehydes.
Answer. (d)
928.
Benzaldehyde can be distinguished from acetophenone by using :
(a)
Tollens' reagent
(b) Lucas reagent
(c)
Fehling's reagent
(d)
All of these
Answer. (a)
929.
Benzaldehyde does not react with
(a) Tollens' reagent
(b)
Phenylhydrazine
(c)
Fehling's solution
(d) NaHSO3
Answer. (c)
930.
Which of the following will
give a positive Tollens' test? (a)
(b)
(c)
(d)
Answer. (c)
931.
Which of the following compounds
yields a yellow precipitate when warmed
with a mixture of iodine in aqueous sodium hydroxide?
(a) Acetophenone
(b)
Benzaldehyde
(c) Benzophenone
(d)
Propanal
Answer. (a)
932.
A
compound (A) gave a positive iodoform
reaction and left a solution containing a monocarboxylate ion.
Which of the following could (A) be?
(a)
(b)
(c)
(d)
Answer. (c)
933.
How many isomers containing a benzene ring correspond to the formula C6H4(COOH)2?
(a) 1
(b) 2
(c) 3
(d) 4
Answer. (c)
934.
Which of the following is not a carboxylic acid?
(a) Malonic acid
(b)
Acetic acid
(c)
Picric acid
(d) Adipic acid
Answer. (c)
935.
Phenylmagnesium bromide reacts with
CO2 followed by acid-hydrolysis to form :
(a) Phenol
(b) Benzoic acid
(c)
Bromobenzene
(d) Acetophenone
Answer. (b)
936.
Benzoic acid and diphenyl
ketone are both solids insoluble in water. A mixture of these compounds can be
separated if we
(a) add the mixture
to a solution of NaOH in water,
and filter.
(b)
add the mixture
to a solution of HCl in water, and filter.
(c) dissolve the mixture in benzene and boil off the benzene.
(d)
It is impossible to separate a
mixture of two solids when both are insoluble in water.
Answer. (a)
937.
Which of the following
reactions does not produce benzene
as one of the products?
(a) Treating benzenediazonium chloride with H3PO2
(b)
Distilling phenol with zinc dust
(c) Fusing sodium
benzoate with NaOH
(d)
Fusing sodium benzenesulfonate with NaOH
Answer. (d)
938.
Which of the following esters produces butyric acid and phenol on hydrolysis?
(a) Phenyl butyrate
(b)
Butyl benzoate
(c)
Benzyl propionate
(d) Phenyl propionate
Answer. (a)
939. Benzoyl chloride on basic-hydrolysis (NaOH/H2O) gives :
(a)
Benzoic acid
(b)
Methyl benzoate
(c) Sodium benzoate
(d)
Ethyl benzoate
Answer. (c)
940. Sodium benzoate
on heating with soda-lime gives :
(a)
Sodium phenoxide
(b) Benzene
(c)
Benzaldehyde
(d)
Benzophenone
Answer. (b)
941.
The product
of the following reaction is :
(a)
(b)
(c)
(d)
Answer. (b)
942. Methyl benzoate
on hydrolysis gives
(a)
Acetic acid
(b)
Benzoic acid
(c) Picric acid
(d)
Phenylacetic acid
Answer. (b)
943.
Aspirin is produced
by heating salicylic
acid with
(a)
acetic anhydride in the presence of phosphoric acid
(b) benzoic anhydride
in the presence of phosphoric acid
(c)
methyl alcohol in the presence
of sulfuric acid
(d)
phenol in the presence of sulfuric acid
Answer. (a)
944.
Oil of Wintergreen (Methyl salicylate) is obtained
by treating salicylic acid with
(a) Methane at 150°C
(b)
CH3OH and conc.
H2SO4
(c) Methyl chloride
(d)
NaOH and then CH3OH
Answer. (b)
945.
Which of the following statements is true :
(a)
o-Nitrobenzoic acid is more acidic than p-nitrophenol
(b) o-Nitrobenzoic acid is less acidic than p-nitrophenol
(c)
o-Nitrobenzoic acid and p-nitrobenzoic acid have the same acid strength
(d)
None of these statements is true
Answer. (a)
946.
The order of increasing acidity
is :
(a) chloroacetic acid > formic acid > benzoic acid
(b)
benzoic acid > formic acid > chloroacetic acid
(c) all are the same
(d)
not determinable from available data
Answer. (a)
947.
Which of the following is the strongest
acid?
(a)
Trichloroacetic acid
(b) Phenol
(c)
Acetic acid
(d)
Benzoic acid
Answer. (a)
948.
Which of the following is the strongest
acid?
(a) Ethanol
(b)
Phenol
(c)
Anisole
(d) Benzoic acid
Answer. (d)
949.
Which acid is weaker than benzoic acid?
(a) p-Methylbenzoic acid
(b)
p-Chlorobenzoic acid
(c) p-Nitrobenzoic acid
(d)
o-Chlorobenzoic acid
Answer. (a)
950.
Compound (A) when reacted with PCl5 and then with ammonia
gave (B). Compound (B) when treated
with bromine and NaOH, produced
(C). Compound
(C) on treatment with NaNO2/HCl at 0°C and then boiling with H2O produced o- cresol.
Compound (A) is
(a) o-Toluic acid
(b) o-Chlorotoluene
(c)
m-Toluic acid
(d)
o-Bromotoluene
Answer. (a)
951.
The reason why materials appear colored is
(a) The selective
absorption of spectral
colors
(b)
The interaction between
the light and the
electrons of the dye molecules
(c)
The composition of the white light from various spectral colors
(d) All of these
Answer. (d)
952.
Which of the following is a chromophore?
(a) –NO2
(b)
–SO3H
(c) –OH
(d)
–COOH
Answer. (a)
953. Which of the following
is an auxochrome?
(a)
–N=O
(b)
–NO2
(c) –N=N–
(d)
–OH
Answer. (d)
954.
The water-solubility of dyes can be increased
by introducing
(a)
SO3Na
groups
(b) COOH groups
(c)
OH groups
(d)
All of these
Answer. (d)
955.
Which dyes become linked to the fibre by
chemical reaction?
(a) Acid dyes
(b)
Direct dyes
(c)
Disperse dyes
(d) None of these
Answer. (a)
956.
All carbon atoms in naphthalene are
(a) sp hybridized
(b)
sp2 hybridized
(c) sp3 hybridized
(d)
None of these
Answer. (b)
957. Naphthalene undergoes oxidation with Na2Cr2O7 / H2SO4 to form
(a)
Phthalic acid
(b)
Phenylacetic acid
(c) Tetralin
(d)
Benzoic acid
Answer. (a)
958.
Naphthalene undergoes reduction with H2 in the presence
of Ni catalyst at high
temperature and pressure to give
(a) Phthalic acid
(b)
Decalin
(c) Benzoic acid
(d)
Tetralin
Answer. (b)
959. Naphthalene
undergoes nitration with HNO3/H2SO4 at 60°C to give
mainly
(a)
1-Nitronaphthalene
(b) 1,2-Dinitronaphthalene
(c)
2-Nitronaphthalene
(d)
1,5-Dinitronaphthalene
Answer. (a)
960.
All carbon atoms in anthracene are
(a)
sp hybridized
(b) sp3 hybridized
(c)
sp2 hybridized
(d) None of these
Answer. (c)
961.
Anthracene undergoes electrophilic substitution reactions mainly at
(a) C-1
(b)
C-2
(c)
C-9
(d) C-1 and C-2
Answer. (c)
962.
Anthracene undergoes oxidation
with O2/V2O5 at 500°C to give
(a) Benzoic acid
(b)
Anthraquinone
(c) Phthalic acid
(d)
Benzophenone
Answer. (b)
963.
Which of the following is not
a heterocyclic compound? (a)
(b)
(c)
(d)
Answer. (c)
964. Which of the following
heterocyclic compounds is not aromatic?
(a)
Pyridine
(b)
Pyrrole
(c) Furan
(d)
Piperidine
Answer. (d)
965. The ‘N’ atom in pyridine is
(a)
sp3 hybridized
(b) sp2 hybridized
(c)
sp hybridized
(d)
cannot be predicted
Answer. (b)
966.
Pyridine has a delocalized π molecular orbital containing
(a)
4 electrons
(b) 6 electrons
(c)
8 electrons
(d) 12 electrons
Answer. (b)
967.
Pyrrole is less basic than
pyridine because the lone-pair of electrons on N- atom in pyrrole
(a) is part of the delocalized π molecular orbital.
(b) is not part of the delocalized π molecular orbital.
(c)
resides in sp2 hybrid orbital
(d)
resides in sp hybrid orbital
Answer. (a)
968.
Pyridine is less basic than
trimethylamine because the lone-pair of electrons on N-atom in pyridine resides
in
(a) sp2 hybrid orbital
(b)
sp hybrid orbital
(c) sp3 hybrid orbital
(d) p-orbital
Answer. (a)
969. Pyridine reacts with HCl to form
(a)
Pyridinium chloride
(b) 2-Chloropyridine
(c)
3-Chloropyridine
(d)
All of these
Answer. (a)
970.
Pyridine undergoes electrophilic
substitution with fuming H2SO4 at 350°C to give
(a) 2-Pyridinesulfonic acid
(b)
4-Pyridinesulfonic
acid
(c) 3-Pyridinesulfonic acid
(d)
None of these
Answer. (c)
971. Pyridine reacts with a mixture of KNO3
and H2SO4 at 300°C to give
(a)
1-Nitropyridine
(b) 2-Nitropyridine
(c)
3-Nitropyridine
(d)
4-Nitropyridine
Answer. (c)
972.
Pyridine undergoes nuclophilic substitution with NaNH2 at 100°C to form
(a)
2-Aminopyridine
(b) 3-Aminopyridine
(c)
4-Aminopyridine
(d)
None of these
Answer. (a)
973.
Which of the following reagents will react with pyrrole to form 2- formylpyrrole?
(a) HCOOH
(b)
CHCl3/KOH
(c) H2O2
(d)
(CH3CO)2O/SnCl4
Answer. (b)
974.
Furan reacts with ammonia in the presence
of alumina at 400°C to give
(a)
Pyridine
(b) Furfural
(c) Pyrrole
(d)
Furoic acid
Answer. (c)
975.
Which of the following reagents
will react with furan to form
2-furansulfonic acid?
(a) SO3 in pyridine at
100°C
(b)
Dilute H2SO4 at 200°C
(c) SO2 at 100°C
(d)
Dilute H2SO4 at 100°C
Answer. (a)
976.
When aniline is heated with glycerol
in the presence of sulfuric
acid and nitrobenzene, it
gives quinoline. This reaction in called
(a) Fischer synthesis
(b)
Skraup synthesis
(c)
Diazotization
(d) Corey-House synthesis
Answer. (b)
977. Quinoline undergoes nucleophilic substitution on heating with NaNH2 to
give
(a)
2-Aminoquinoline
(b)
4-Aminoquinoline
(c) 3-Aminoquinoline
(d)
8-Aminoquinoline
Answer. (a)
978. Orlon is prepared by the polymerisation of
(a)
Vinyl cyanide
(b) Allyl alcohol
(c)
Vinyl chloride
(d)
Allyl chloride
Answer. (a)
979.
Which of the following statements is true about terpenes?
(a)
They are a class of lipids that can be isolated from plants.
(b) They contain
carbon atoms in multiples of five.
(c)
They are composed
of isoprene units joined together
in a head-to-tail fashion.
(d) All of the above
Answer. (d)
980.
How many isoprene
units are in a sesquiterpene?
(a) 1
(b) 2
(c) 3
(d) 4
Answer. (c)
981. What is the IUPAC name for isoprene?
(a)
1,3-pentadiene
(b)
2,4-pentadiene
(c) 2,3-dimethyl-1, 3-butadiene
(d)
2-methyl-1,3-butadiene
Answer. (d)
982. How many isoprene units are present in sesquiterpenes?
(a) 1
(b) 2
(c) 3
(d) 4
Answer. (c)
983.
Teflon is prepared
by the polymerization of
(a)
Butadiene
(b) Vinyl cyanide
(c)
Vinyl chloride
(d) Tetrafluoroethylene
Answer. (d)
984.
Bakelite is obtained
from :
(a) Phenol and formaldehyde
(b)
Adipic acid and hexamethylene diamine
(c)
Dimethyl terephthalate and ethylene glycol
(d) Neoprene
Answer. (a)
985. Nylon-6,6 is obtained from :
(a)
Adipic acid and hexamethylene diamine
(b)
Tetrafluoroethylene
(c) Vinyl cyanide
(d)
Vinylbenzene
Answer. (a)
986. Neoprene is a polymer of the following monomer
(a)
Chloroprene
(b) Isoprene
(c) Isobutane
(d)
Isopentene
Answer. (a)
987.
Which of the following is a thermosetting polymer?
(a) Bakelite
(b)
Nylon-6,6
(c)
Polyethylene
(d) Teflon
Answer. (a)
988.
Which of the following is an example
of a condensation polymer?
(a) Nylon-6,6
(b)
Teflon
(c) Polypropylene
(d)
Orlon
Answer. (a)
989. Which of the following
polymers contain nitrogen
(a)
PVC
(b)
Teflon
(c) Nylon
(d)
Terylene
Answer. (c)
990.
Adipic acid
reacts with hexamethylene diamine to form
(a)
Bakelite
(b) Nylon-6,6
(c)
Terylene
(d)
Nylon-6,8
Answer. (b)
991.
Ethylene glycol reacts
with dimethyl terephthalate to form
(a) Nylon-6,6
(b)
Teflon
(c)
Dacron
(d) Orlon
Answer. (c)
992.
Natural rubber is a polymer of
(a) Propene
(b)
Isoprene
(c) Formaldehyde
(d) Phenol
Answer. (b)
993. The monomers for Buna-S are
1,3-butadiene and
(a)
Ethylene glycol
(b) Adipic acid
(c)
Styrene
(d)
Caprolactum
Answer. (c)
994.
Which of the following statements is not true?
(a)
Natural rubber is a hydrocarbon.
(b) Natural rubber is made of isoprene
units
(c)
Natural rubber is a polymer of 1,3-Butadiene
(d) Natural rubber can be vulcanized.
Answer. (c)
995.
Which of the following are addition polymers?
I.
Polypropylene
II.
Teflon
III.
Nylon
(a) Only I
(b)
Only II
(c) Only III
(d)
both I and II
Answer. (d)
996. Which of the following
are condensation polymers?
I.
Polypropylene
II.
Teflon
III.
Nylon
(a)
Only I
(b) Only II
(c)
Only III
(d)
Both II and III
Answer. (c)
997.
Which one
of the following is used to make
Teflon?
(a)
Fluoroethene
(b) 1,1,4,4-tetrafluorobutadiene
(c)
1,2-difluoroethene
(d) Tetrafluoroethylene
Answer. (d)
998.
Vulcanization is the process of cross-linking polymer
chains in rubber
using
(a) Sulfur.
(b)
Formaldehye.
(c) Benzoyl peroxide.
(d)
Ethylene glycol.
Answer. (a)
999. What is the purpose
of plasticizers?
(a)
Harden plastics
(b)
Soften plastics
(c) Initiate polymerizations
(d)
Cross-link polymer chains
Answer. (b)
1000. Polymers which soften on heating and harden when cooled are
(a)
Cross-linked polymers
(b) Copolymers
(c)
Thermosetting polymers
(d)
Thermoplastics
Answer. (d)