429 Sample
429 Sample
429 Sample
1
Copyright © 2017 Pearson Education, Inc.
5) The structure below is a potent analgesic agent (pain reliever) (J. Med. Chem., 2009, 5685).
How many secondary carbons are in this structure?
A) 2
B) 4
C) 6
D) 12
Answer: A
Diff: 2
Section: 3.3
GO: G5
6) If an acyclic alkane hydrocarbon contains n carbon atoms, how many hydrogen atoms must it
also contain?
A) n
B) 2n
C) n + 2
D) 2n + 2
E) n - 2
Answer: D
Diff: 2
Section: 3.2
LO: 3.1
GO: G2
7) A series of compounds, like the n-alkanes, that differ only by the number of groups, is
called a(n) ________ series.
Answer: homologous
Diff: 2
Section: 3.2
LO: 3.1
2
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8) A bicyclic alkane contains 12 carbon atoms. How many hydrogen atoms does it contain?
A) 20
B) 22
C) 24
D) 26
E) 28
Answer: B
Diff: 2
Section: 3.10
LO: 3.1
10) Triacontane is an unbranched alkane that contains 30 carbon atoms in each molecule. How
many hydrogen atoms are present in each molecule of triacontane?
A) 30
B) 32
C) 58
D) 60
E) 62
Answer: E
Diff: 3
Section: 3.2
LO: 3.1
3
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12) Provide an acceptable name for (CH3CH2CH2)3CH.
Answer: 4-propylheptane
Diff: 1
Section: 3.3
LO: 3.2
MCAT LO: MCAT3.1
Answer: 3-fluoro-2,2-dimethylhexane
Diff: 1
Section: 3.3
LO: 6.1
MCAT LO: MCAT6.1
Answer: 2,3,6,7-tetramethylnonane
Diff: 1
Section: 3.3
LO: 3.2
MCAT LO: MCAT3.1
CH3CH2CH2CH2CH2CH3
Answer: hexane or n-hexane
Diff: 1
Section: 3.3
LO: 3.2
MCAT LO: MCAT3.1
4
Copyright © 2017 Pearson Education, Inc.
16) Provide an acceptable name for the alkane shown below.
Answer: 2,5-dimethylheptane
Diff: 1
Section: 3.3
LO: 3.2
MCAT LO: MCAT3.1
Diff: 1
Section: 3.3
LO: 3.1
MCAT LO: MCAT3.1
Diff: 1
Section: 3.3
LO: 3.1
MCAT LO: MCAT3.1
19) A student named the following molecule "4-isobutylheptane." Why is this incorrect? What is
the correct name?
Answer: 2-methyl-4-propylheptane is the correct name. The name was incorrect because
although heptane is the longest chain in both names, the substituent isobutyl is branched, while
methyl and propyl are not.
Diff: 1
Section: 3.3
LO: 3.1
GO: G2
MCAT LO: MCAT3.1
5
Copyright © 2017 Pearson Education, Inc.
20) Name the haloalkane shown.
Answer: 3,4-dibromoheptane
Diff: 1
Section: 3.3
LO: 6.1
MCAT LO: MCAT6.1
Answer: 4,4-dichloro-6-isopropyl-3-methylnonane
Diff: 2
Section: 3.3
LO: 3.2
MCAT LO: MCAT3.1
6
Copyright © 2017 Pearson Education, Inc.
24) Provide the IUPAC name of (CH3)2CHCH2CH2C(CH3)3.
Answer: 2,2,5-trimethylhexane
Diff: 2
Section: 3.3
LO: 3.2
MCAT LO: MCAT3.1
Answer: 3-ethyl-4,4-dimethylheptane
Diff: 2
Section: 3.3
LO: 3.2
MCAT LO: MCAT3.1
7
Copyright © 2017 Pearson Education, Inc.
29) Draw an acceptable structure for 6-ethyl-2,6,7-trimethyl-5-propylnonane.
Answer:
Diff: 2
Section: 3.3
LO: 3.1
MCAT LO: MCAT3.1
Answer: 2,2,3,6-tetramethylheptane
Diff: 2
Section: 3.3
LO: 3.2
MCAT LO: MCAT3.1
Answer: 6-ethyl-2-methyl-5-propyldecane
Diff: 2
Section: 3.3
LO: 3.2
MCAT LO: MCAT3.1
8
Copyright © 2017 Pearson Education, Inc.
32) Provide an acceptable name for the alkane shown below.
Answer: 2-fluoro-7-methyl-5-propyldecane
Diff: 2
Section: 3.3
LO: 6.1
MCAT LO: MCAT6.1
33) Identify the correct IUPAC name for the following structures.
A) 4-(2-iodo-1-methylethyl)-3-methylheptane
B) 3-s-butyl-1-iodo-2-methylhexane
C) 1-iodo-2,4-dimethyl-3-propylhexane
D) 2,4-dimethyl-1-iodo-3-propylhexane
Answer: A
Diff: 2
Section: 3.3
LO: 6.1
GO: G2
MCAT LO: MCAT6.1
CH3CH2C(CH3)2CH2CH2I
Answer: 1-iodo-3,3-dimethylpentane
Diff: 2
Section: 3.3
LO: 6.1
MCAT LO: MCAT6.1
[(CH3)2CH]2CHCH3
Answer: 2,3,4-trimethylpentane
Diff: 2
Section: 3.3
LO: 3.1
MCAT LO: MCAT3.1
9
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36) Name the alkane shown.
Answer: 5-ethyl-2,2-dimethyloctane
Diff: 2
Section: 3.3
LO: 3.2
MCAT LO: MCAT3.1
38) Identify the correct IUPAC name for the following structure.
A) 6-bromo-1-cyclopentyl-3,6-dimethylhexane
B) 1-bromo-5-cyclopentyl-1,4-dimethylpentane
C) 2-bromo-6-cyclopentyl-5-methylhexane
D) 5-bromo-1-cyclopentyl-2-methylhexane
E) none of the above
Answer: D
Diff: 3
Section: 3.10
LO: 6.1
GO: G2
MCAT LO: MCAT6.1
10
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39) Identify the correct IUPAC name for each compound shown below.
A) 2-bromo-3-sec-butyl-4-ethylhexane
B) 2-bromo-4-ethyl-3-sec-butylhexane
C) 3-(1-bromoethyl)-2,4-diethylhexane
D) 4-(1-bromoethyl)-3-ethyl-5-methylheptane
E) 4-(1-bromoethyl)-5-ethyl-3-methylheptane
Answer: D
Diff: 3
Section: 3.3
LO: 6.1
GO: G2
MCAT LO: MCAT6.1
Answer: 2,2,7-trichloro-4-ethyl-6-isobutyl-7,10-dimethyldodecane
Diff: 3
Section: 3.3
LO: 6.1
MCAT LO: MCAT6.1
41) Give structures for the three isomers with molecular formula C5H12 and provide the
common name of each.
Answer:
Diff: 3
Section: 3.3
LO: 3.2
GO: G7
MCAT LO: MCAT3.2
11
Copyright © 2017 Pearson Education, Inc.
42) Provide an acceptable name for the alkane shown below.
Answer: 3-ethyl-7-methyl-5-propylnonane
Diff: 3
Section: 3.3
LO: 3.2
MCAT LO: MCAT3.1
Diff: 3
Section: 3.3
LO: 3.1
MCAT LO: MCAT3.1
Diff: 3
Section: 3.10
LO: 3.1
MCAT LO: MCAT3.1
45) When one compares the densities of n-hexane and water, one finds ________.
A) that n-hexane is less dense than water
B) that n-hexane is more dense than water
C) that these two compounds have the same density
D) that the relative densities of two immiscible compounds cannot be measured
Answer: A
Diff: 1
Section: 3.4
LO: 3.3
MCAT LO: MCAT3.3
12
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46) A branched alkane has ________ boiling point relative to the isomeric linear alkane. There
are ________ London force interactions in the branched alkane.
A) a higher; stronger
B) a higher; weaker
C) a lower, stronger
D) a lower; weaker
E) the same; similar
Answer: D
Diff: 1
Section: 3.4
LO: 3.3
MCAT LO: MCAT3.3
47) 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
E) n-hexane < 2,3-dimethylbutane < 2-methylpentane
Answer: A
Diff: 2
Section: 3.4
LO: 3.3
GO: G7
MCAT LO: MCAT3.3
48) Name the following compound and use the appropriate cis/trans designation.
49) ________ is the n-alkane of greatest molecular weight which is a gas at room temperature
and pressure.
Answer: Butane
Diff: 2
Section: 3.4
LO: 3.3
MCAT LO: MCAT3.3
13
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50) Place the following alkanes in order of increasing boiling point:
52) Which intermolecular force is primarily responsible for the interactions among alkane
molecules?
Answer: van der Waals or London forces
Diff: 2
Section: 3.7
LO: 3.3
MCAT LO: MCAT3.3
54) Within the context of commercial uses of alkanes, explain what "knocking" is.
Answer: "Knocking" is the potentially damaging, premature explosive combustion of certain
gasoline mixtures in a car's engine.
Diff: 1
Section: 3.5
LO: 3.3
GO: G5
MCAT LO: MCAT3.3
14
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55) Explain why the lowest energy conformation of decane is an extended, or zig-zag
conformation.
Answer: The lowest-energy conformation for any straight-chain alkane is the one with all the
internal carbon-carbon bonds in their anti conformations. These anti conformations give the
chain a zigzag shape.
Diff: 1
Section: 3.9
LO: 3.4
GO: G8
MCAT LO: MCAT3.4
56) Which alkanes have largely replaced Freons as propellants in aerosol cans?
A) methane and ethane
B) propane and butane
C) pentane and hexane
D) nonane and decane
E) none of the above
Answer: B
Diff: 2
Section: 3.5
LO: 3.3
GO: G5
MCAT LO: MCAT3.3
57) How many carbons do the primary alkane constituents of gasoline contain?
A) C1—C2
B) C3—C4
C) C5—C8
D) C8—C12
E) C12—C16
Answer: C
Diff: 2
Section: 3.5
LO: 3.3
GO: G5
MCAT LO: MCAT3.3
58) ________ is the reaction process through which long-chain alkanes are converted into a
mixture of short-chain alkanes and alkenes.
Answer: Catalytic cracking
Diff: 2
Section: 3.5
GO: G5
15
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59) List three commercial products which are composed primarily of alkanes.
Answer: natural gas, gasoline, kerosene, heating oil, lubricating oil, liquefied petroleum gas, jet
fuel, diesel oil, petroleum jelly
Diff: 2
Section: 3.5
LO: 3.3
GO: G5
MCAT LO: MCAT3.3
60) Linear alkanes generally have higher phase transitions than their branched isomers. However,
the melting point of cyclohexane is 6° C while the melting point of hexane is -95° C. Briefly
suggest a reason why this is.
Answer: Cyclohexane is more symmetric molecule and doesn't have as many degrees of
freedom or conformational flexibility as hexane. This allows it to pack in a more regular lattice
and has stronger IMFs between the molecules and therefore a higher boiling point.
Diff: 2
Section: 3.5
LO: 3.3
GO: G5
MCAT LO: MCAT3.3
61) In the complete combustion of heptane, how many moles of water are produced?
Answer: 8
Diff: 2
Section: 3.6
LO: 3.1
GO: G7
62) By using the appropriate molecular formulas, write a balanced equation which describes the
complete combustion of cyclohexane.
Answer: C6H12 + 9 O2 → 6 CO2 + 6 H2O
Diff: 2
Section: 3.6
LO: 3.1
GO: G7
16
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63) When a mole of decane undergoes complete combustion, how many moles of water are
formed?
A) 1
B) 10
C) 11
D) 15.5
E) 22
Answer: C
Diff: 2
Section: 3.6
LO: 3.1
GO: G7
64) By using the appropriate molecular formulas, write a balanced equation which describes the
complete combustion of nonane.
Answer: CH3(CH2)7CH3 + 14 O2 → 9 CO2 + 10 H2O
Diff: 3
Section: 3.6
LO: 3.1
GO: G7
65) The energy barrier for carbon-carbon bond rotation in propane is mainly due to ________.
A) angle strain
B) bond strain
C) muscle strain
D) steric strain
E) torsion strain
Answer: E
Diff: 1
Section: 3.7
LO: 3.4
17
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66) The structures below are ________.
A) not isomers
B) conformational isomers
C) cis-trans isomers
D) structural isomers
E) both B and D
Answer: D
Diff: 2
Section: 3.7
LO: 2.4
GO: G5
MCAT LO: MCAT2.4
67) Which of the following best describes the molecules of a sample of ethane gas at room
temperature?
A) Almost all of the molecules are frozen or locked in the eclipsed conformation.
B) Almost all of the molecules are frozen or locked in the staggered conformation.
C) The molecules are rapidly interconverting between the eclipsed and staggered conformations,
but at any one time slightly more of them are present in the eclipsed conformation.
D) The molecules are rapidly interconverting between the eclipsed and staggered conformations,
but at any one time slightly more of them are present in the staggered conformation.
Answer: D
Diff: 2
Section: 3.7
LO: 3.4
GO: G2
Diff: 2
Section: 3.7
LO: 3.4
MCAT LO: MCAT3.4
18
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69) Define the term conformation.
Answer: Conformations are different arrangements of the same molecule formed by rotations
about single bonds.
Diff: 2
Section: 3.7
Diff: 2
Section: 3.7
GO: G2
71) Draw the Newman projection of the highest energy conformation that results from rotation
about the C2-C3 bond of 2,2-dimethylbutane.
Answer:
Diff: 1
Section: 3.8
LO: 3.4
MCAT LO: MCAT3.4
72) Which of the following statements concerning the conformers of butane is true?
A) Unlike ethane, all butane conformers are classified as eclipsed.
B) The lowest energy conformer of butane is the gauche conformer.
C) There is more torsional strain in the anti conformer than in the totally eclipsed conformer.
D) The eclipsed and totally eclipsed conformers have the same amount of nonbonded strain.
E) The gauche and anti conformers differ primarily in the amount of nonbonded strain present.
Answer: E
Diff: 2
Section: 3.8
LO: 3.4
GO: G7
MCAT LO: MCAT3.4
19
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73) Convert the Newman structure below to the equivalent line-angle structure.
Answer:
Diff: 2
Section: 3.8
LO: 3.4
MCAT LO: MCAT3.4
Diff: 2
Section: 3.8
LO: 3.4
GO: G2
MCAT LO: MCAT3.4
75) Draw the Newman projection of the highest energy conformation that results from rotation
about the C2-C3 bond of 2-methylbutane.
Answer:
Diff: 2
Section: 3.8
LO: 3.4
GO: G2
MCAT LO: MCAT3.4
20
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76) Consider rotation about the C3-C4 bond of hexane, and draw the Newman projection for the
most stable conformation.
Answer:
Diff: 2
Section: 3.9
LO: 3.4
GO: G2
MCAT LO: MCAT3.4
77) Arrange the following conformers of butane in order of energy, lowest to highest: eclipsed,
totally eclipsed, gauche, and anti.
Answer: anti < gauche < eclipsed < totally eclipsed
Diff: 2
Section: 3.8
LO: 3.4
GO: G2
MCAT LO: MCAT3.4
78) Among the butane conformers, which occur at energy minima on a graph of potential energy
versus dihedral angle?
A) gauche only
B) eclipsed and totally eclipsed
C) gauche and anti
D) eclipsed only
E) anti only
Answer: C
Diff: 3
Section: 3.8
LO: 3.4
MCAT LO: MCAT3.4
21
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79) Which line angle drawing best represents the Newman Projection shown below?
A)
B)
C)
D)
Answer: C
Diff: 3
Section: 3.8
LO: 3.4
MCAT LO: MCAT3.4
22
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80) Without any change in conformation, translate the Newman projection shown below to a
perspective structure.
Answer:
Diff: 3
Section: 3.9
LO: 3.4
MCAT LO: MCAT3.4
81) View a butane molecule along the C2—C3 bond and provide a Newman projection of the
lowest energy conformer.
Answer:
Diff: 3
Section: 3.8
LO: 3.4
GO: G2
MCAT LO: MCAT3.4
Diff: 2
Section: 3.8
LO: 3.4
GO: G2
MCAT LO: MCAT3.4
23
Copyright © 2017 Pearson Education, Inc.
83) From the perspective of viewing down the C2—C3 bond, draw the Newman projection of
the most stable conformation of 2,3-dimethylbutane.
Answer:
Diff: 3
Section: 3.8
LO: 3.4
GO: G2
MCAT LO: MCAT3.4
84) From the perspective of viewing down the C2-C3 bond, draw the Newman projection of the
least stable conformation of 2,3-dimethylbutane.
Answer:
Diff: 3
Section: 3.8
LO: 3.4
GO: G2
MCAT LO: MCAT3.4
85) In a Newman projection, siting down the C3-C4 bond, draw the structure below in its most
stable conformation.
Answer:
Diff: 3
Section: 3.9
GO: G2
24
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86) If a monocyclic alkane hydrocarbon contains n carbon atoms, how many hydrogen atoms
must it also contain?
A) n
B) 2n
C) n + 2
D) 2n + 2
E) n - 2
Answer: B
Diff: 1
Section: 3.10
LO: 3.1
GO: G2
87) Give the IUPAC name for the cycloalkane shown below.
Answer: trans-1-ethyl-2-methylcyclopentane
Diff: 1
Section: 3.11
LO: 3.2
MCAT LO: MCAT3.1
88) Give the IUPAC name for the cycloalkane shown below.
Answer: cis-1-isopropyl-3-methylcycloheptane
Diff: 1
Section: 3.11
LO: 3.2
MCAT LO: MCAT3.1
89) What element of ring strain exists in cyclooctane but not in cyclopropane?
Answer: transannular strain
Diff: 1
Section: 3.10
LO: 3.5
GO: G2
25
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90) Provide an acceptable name for the following compound.
Answer: sec-butylcycloheptane
Diff: 2
Section: 3.10
LO: 3.2
MCAT LO: MCAT3.1
92) Identify the correct IUPAC name for the structure shown below.
A) 1-tert-butyl-2-chloro-5-bromocycloheptane
B) 5-bromo-1-tert-butyl-2-chlorocycloheptane
C) 1-bromo-4-chloro-5-tertbutylcycloheptane
D) 1-bromo-4-tert-butyl-5-chlorocycloheptane
E) 1-tert-butyl-4-bromo-7-chlorocycloheptane
Answer: B
Diff: 3
Section: 3.10
LO: 6.1
MCAT LO: MCAT6.1
26
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93) Given the following heats of combustion per CH2 group within the structure, which cyclic
alkane has essentially no angle strain? (Ref: long-chain Alkane = 659 kJ/mol)
A) cyclobutane = 686 kJ/mol
B) cyclopentane = 664 kJ/mol
C) cyclohexane = 659 kJ/mol
D) cycloheptane = 662 kJ/mol
E) cyclooctane = 663 kJ/mol
Answer: C
Diff: 1
Section: 3.12
LO: 3.5
94) Which of the following cycloalkanes exhibits the greatest molar heat of combustion?
A) cyclooctane
B) cycloheptane
C) cyclohexane
D) cyclobutane
E) cyclopropane
Answer: A
Diff: 2
Section: 3.12
95) Which of the following correctly ranks the cycloalkanes in order of increasing ring strain per
methylene?
A) cyclopropane < cyclobutane < cyclohexane < cyclopentane
B) cyclohexane < cyclopentane < cyclobutane < cyclopropane
C) cyclohexane < cyclobutane < cyclopentane < cyclopropane
D) cyclopentane < cyclopropane < cyclobutane < cyclohexane
E) cyclopropane < cyclopentane < cyclobutane < cyclohexane
Answer: B
Diff: 2
Section: 3.12
LO: 3.5
96) Which of the following cycloalkanes has the smallest heat of combustion per CH2 group?
A) cyclopropane
B) cyclobutane
C) cyclopentane
D) cyclohexane
E) cycloheptane
Answer: D
Diff: 2
Section: 3.12
LO: 3.5
27
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97) Which of the following statements regarding cyclobutane is correct?
A) The lowest energy conformation of cyclobutane is a planar one in which all of the bond
angles is 90°.
B) The lowest energy conformation of cyclobutane is known as the chair conformation.
C) The lowest energy conformation is one in which the bond angles are slightly less than 90°
even though this increases angle strain.
D) The lowest energy conformation is one in which the bond angles are greater than 90° so that
angle strain is significantly reduced.
E) None of the above statements is correct.
Answer: C
Diff: 3
Section: 3.12
LO: 3.5
99) Describe the sources of angle strain and torsional strain present in cyclopropane.
Answer: The angle strain arises from the compression of the ideal tetrahedral bond angle of
109.5° to 60°. The large torsional strain occurs since all C—H bonds on adjacent carbons are
eclipsed.
Diff: 3
Section: 3.12
LO: 3.5
100) The twisted boat conformation of cyclohexane is actually a slightly lower energy
conformation than the boat conformation. Which of the following accurately describes one
factor involved in this structural behavior?
A) lower angle strain in the boat
B) higher torsional strain in the twisted boat
C) fewer unfavorable steric factors in the twisted boat
D) increased rotational freedom in the boat
E) lower bond strain in the boat
Answer: C
Diff: 1
Section: 3.13
LO: 3.5
28
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101) Draw the chair conformer of cyclohexane. Label the axial hydrogens (Ha) and the
equatorial hydrogens (He).
Answer:
Diff: 1
Section: 3.13
LO: 3.7
102) In the boat conformation of cyclohexane, the "flagpole" hydrogens are located ________.
A) on the same carbon
B) on adjacent carbons
C) on C-1 and C-3
D) on C-1 and C-4
E) none of the above
Answer: D
Diff: 2
Section: 3.13
LO: 3.7
103) Which of the following correctly lists the conformations of cyclohexane in order of
increasing energy?
A) chair < boat < twist < half-chair
B) half-chair < boat < twist < chair
C) chair < twist < half-chair < boat
D) chair < twist < boat < half-chair
E) half-chair < twist < boat < chair
Answer: D
Diff: 3
Section: 3.13
LO: 3.7
29
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104) Consider the equilibrium shown below. When one looks at the equilibrium where X = CH3
and the one where X = CH(CH3)2, how do the values of the equilibrium constants (Ks)
compare?
105) Draw isopropylcyclohexane in a chair conformation and then draw its ring flipped isomer.
Label the substituent as either axial or equitorial. Indicate which of the conformers is more
stable.
Answer:
Diff: 3
Section: 3.14
LO: 3.7
106) In the lowest energy chair conformation of cis-1,3-dimethylcyclohexane, how many axial
positions are occupied by hydrogen atoms?
A) 2
B) 3
C) 4
D) 5
E) 6
Answer: E
Diff: 3
Section: 3.15
LO: 3.7
30
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107) Which of the following statements is a correct description of the most stable conformation
of 1,1,3-trimethylcyclohexane?
A) The methyl group at C-3 is equatorial.
B) C-1 is a tertiary carbon and C-3 is a primary carbon.
C) C-1 is a quaternary carbon and C-3 is a secondary carbon.
D) C-1 is a tertiary carbon and C-3 is a secondary carbon.
E) Both methyl groups at C-1 are equatorial.
Answer: A
Diff: 2
Section: 3.15
LO: 3.7
108) Which of the statements below correctly describes the chair conformations of
109) Which of the statements below correctly describes the chair conformations of
31
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110) In the lowest energy conformation of the compound below, how many alkyl substituents are
equatorial?
A) 0
B) 1
C) 2
D) 3
E) 6
Answer: C
Diff: 2
Section: 3.15
LO: 3.7
111) In the lowest energy conformation of the compound below, how many alkyl substituents are
axial?
A) 0
B) 1
C) 2
D) 3
E) 6
Answer: A
Diff: 2
Section: 3.15
LO: 3.7
GO: G2
32
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112) Assuming a chair conformation, which of the following configurations will always have
both methyl groups in relative axial/equatorial positions?
A) trans-1,3-dimethylcyclohexane
B) cis-1,3-dimethylcyclohexane
C) cis-1,2-dimethylcyclohexane
D) trans-1,2-dimethylcyclohexane
E) Both B and D are correct.
F) Both A and C are correct.
Answer: F
Diff: 2
Section: 3.15
LO: 3.7
GO: G2
Diff: 2
Section: 3.15
LO: 3.7
Answer:
Diff: 2
Section: 3.15
LO: 3.7
33
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115) Draw the most stable conformation of cis-1,4-dipropylcyclohexane.
Answer:
Diff: 2
Section: 3.15
LO: 3.7
MCAT LO: MCAT3.4
Diff: 2
Section: 3.15
LO: 3.7
MCAT LO: MCAT3.4
Diff: 2
Section: 3.15
LO: 3.7
MCAT LO: MCAT3.4
Diff: 2
Section: 3.15
LO: 3.7
MCAT LO: MCAT3.4
Diff: 2
Section: 3.15
LO: 3.7
MCAT LO: MCAT3.4
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120) Draw the most stable conformation of cis-1-ethyl-3-methylcyclohexane.
Answer:
Diff: 2
Section: 3.15
LO: 3.7
MCAT LO: MCAT3.4
Diff: 2
Section: 3.15
LO: 3.7
MCAT LO: MCAT3.4
122) Which of the following difluorocyclohexane isomers has the greatest molecular dipole in its
least stable chair conformation?
A) cis 1,2-difluorocyclohexane
B) trans 1,2-difluorocyclohexane
C) cis 1,3-difluorocyclohexane
D) trans 1,3-difluorocyclohexane
Answer: C
Diff: 3
Section: 3.15
LO: 3.7
GO: G7
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124) With each structure below drawn in its most stable chair conformation, identify the
sequence that ranks the structures in order of increasing stability.
A) 1 < 2 < 3
B) 2 < 3 < 1
C) 3 < 1 < 2
D) 2 < 1 < 3
Answer: D
Diff: 3
Section: 3.15
LO: 3.7
GO: G2
125) Circle all substituents that would be expected to occupy an axial position in the fused
bicyclic structure below.
Answer:
Diff: 3
Section: 3.16
LO: 3.7
GO: G2
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126) Which of the following is a bridged bicyclic alkane?
A) cis-decalin
B) bicyclo[2.2.1]heptane
C) bicyclo[3.2.0]heptane
D) bicyclo[4.1.0]heptane
E) none of the above
Answer: B
Diff: 2
Section: 3.16
LO: 3.3
A) bridged bicyclic
B) fused bicyclic
C) spiro bicyclic
D) bridged tricyclic
Answer: A
Diff: 2
Section: 3.16
LO: 3.3
Answer: Bicyclo[2.1.1]hexane
Diff: 2
Section: 3.16
LO: 3.2
GO: G2
MCAT LO: MCAT3.1
Diff: 3
Section: 3.16
LO: 3.2
GO: G2
MCAT LO: MCAT3.1
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130) Draw the most stable conformation of trans-decalin.
Answer:
Diff: 3
Section: 3.16
LO: 3.7
GO: G2
A) I<III<II<IV
B) IV<II<III<I
C) III<I<IV<II
D) II<IV<I<III
Answer: A
Diff: 3
Section: 3.8
LO: 3.4
GO: G2
MCAT LO: MCAT3.4
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132) Which line-angle formula corresponds to the chair conformation shown below?
A) I
B) II
C) III
D) IV
Answer: C
Diff: 2
Section: 3.15
LO: 3.7
GO: G2
133) Draw a Newman Projection along the C3-C4 for the molecule shown below. (C3 should be
in front.)
Answer:
Diff: 2
Section: 3.9
LO: 3.4
GO: G2
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134) Draw a Newman Projection along the C3-C4 for the molecule shown below. (C3 should be
in front.)
Answer:
Diff: 2
Section: 3.9
LO: 3.4
GO: G2
Answer: FALSE
Diff: 2
Section: 3.7
LO: 2.4
GO: G5
MCAT LO: MCAT2.4
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