Deck 4: Cycloalkanes

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Question
Which of the following compounds has the highest heat of combustion per CH2 group?

A) cyclopropane
B) cyclobutane
C) cyclopentane
D) cyclohexane
E) All have equal Hcombustion.
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Question
The most stable conformation of cis-1,3-dimethylcyclohexane has how many hydrogen atoms in axial positions?

A) 4
B) 5
C) 6
D) 8
E) None of the above.
Question
Which of the following correctly shows the Newman projection along a C-C bond in cyclohexane? (the squiggles indicate where the rest of the ring is attached) <strong>Which of the following correctly shows the Newman projection along a C-C bond in cyclohexane? (the squiggles indicate where the rest of the ring is attached)  </strong> A) A B) B C) C D) D E) E <div style=padding-top: 35px>

A) A
B) B
C) C
D) D
E) E
Question
Which of the following statements about conformations of methylcyclohexane is true? <strong>Which of the following statements about conformations of methylcyclohexane is true?  </strong> A) The energy barrier to interconvert these is too high to be achieved at room temperature. B) The two forms are in equilibrium and are present in equal amounts at room temperature. C) The two forms are not in equilibrium but are present in equal amounts at room temperature. D) The two forms are in equilibrium but are not present in equal amounts at room temperature. E) The two forms are not in equilibrium and are not present in equal amounts at room temperature. <div style=padding-top: 35px>

A) The energy barrier to interconvert these is too high to be achieved at room temperature.
B) The two forms are in equilibrium and are present in equal amounts at room temperature.
C) The two forms are not in equilibrium but are present in equal amounts at room temperature.
D) The two forms are in equilibrium but are not present in equal amounts at room temperature.
E) The two forms are not in equilibrium and are not present in equal amounts at room temperature.
Question
Which of the following isomers would you expect to have the lowest heat of combustion? (i.e.,be most stable)

A) cis-1,2-dimethylcyclohexane
B) trans-1,3-dimethylcyclohexane
C) cis-1,4-dimethylcyclohexane
D) cis-1,3-dimethylcyclohexane
E) All should have the same heat of combustion.
Question
Which of the following cyclic alkanes can be ring-opened under hydrogenation conditions? <strong>Which of the following cyclic alkanes can be ring-opened under hydrogenation conditions?  </strong> A) cyclopropane B) cyclobutane C) cyclopentane D) cyclohexane E) more than one of these <div style=padding-top: 35px>

A) cyclopropane
B) cyclobutane
C) cyclopentane
D) cyclohexane
E) more than one of these
Question
Which of the following compounds has the lowest heat of combustion per CH2 group?

A) cyclopropane
B) cyclobutane
C) cyclopentane
D) cyclohexane
E) All have equal Hcombustion.
Question
Which one of the following cyclic alkanes has the greatest tendency to have a planar ring?

A) cyclopropane
B) cyclobutane
C) cyclopentane
D) cyclohexane
E) None of the above are planar.
Question
Which would be the most stable conformation of trans-1-methyl-3-isopropylcyclohexane?

A)
<strong>Which would be the most stable conformation of trans-1-methyl-3-isopropylcyclohexane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which would be the most stable conformation of trans-1-methyl-3-isopropylcyclohexane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which would be the most stable conformation of trans-1-methyl-3-isopropylcyclohexane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which would be the most stable conformation of trans-1-methyl-3-isopropylcyclohexane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which would be the most stable conformation of trans-1-methyl-3-isopropylcyclohexane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which,if either,of the two isomers of the compound shown below would be more stable? <strong>Which,if either,of the two isomers of the compound shown below would be more stable?  </strong> A) Cis is more stable. B) Trans is more stable. C) Both are equally stable. D) Neither is stable. E) There is no way to predict this. <div style=padding-top: 35px>

A) Cis is more stable.
B) Trans is more stable.
C) Both are equally stable.
D) Neither is stable.
E) There is no way to predict this.
Question
Which of the following disubstituted cyclohexanes could exist in a conformation that has both groups equatorial?

A) cis-1,3-dimethylcyclohexane
B) cis-1,4-dimethylcyclohexane
C) trans-1,3-dimethylcyclohexane
D) cis-1,2-dimethylcyclohexane
E) All or none can have both groups equatorial.
Question
What would be the name of the following? <strong>What would be the name of the following?  </strong> A) 5-cyclopentyl-1-methylcyclononane B) cis-1-cyclopentyl-5-methylcyclodecane C) cis-5-methyl-1-cyclopentylcyclododecane D) trans-cyclopentyl-5-methylcyclodecane E) (5-methylcyclodecyl)cyclopentane <div style=padding-top: 35px>

A) 5-cyclopentyl-1-methylcyclononane
B) cis-1-cyclopentyl-5-methylcyclodecane
C) cis-5-methyl-1-cyclopentylcyclododecane
D) trans-cyclopentyl-5-methylcyclodecane
E) (5-methylcyclodecyl)cyclopentane
Question
Terpenes can be considered to be built up from what units?

A)
<strong>Terpenes can be considered to be built up from what units?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Terpenes can be considered to be built up from what units?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Terpenes can be considered to be built up from what units?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Terpenes can be considered to be built up from what units?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Terpenes can be considered to be built up from what units?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following ring systems belongs to the class of compounds called steroids?

A)
<strong>Which of the following ring systems belongs to the class of compounds called steroids?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which of the following ring systems belongs to the class of compounds called steroids?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which of the following ring systems belongs to the class of compounds called steroids?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which of the following ring systems belongs to the class of compounds called steroids?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which of the following ring systems belongs to the class of compounds called steroids?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What is the correct IUPAC name for the following molecule: <strong>What is the correct IUPAC name for the following molecule:  </strong> A) 1-ethyl-2-methylhexane B) 2-ethyl-1-methylcycloheptane C) 4-ethyl-5-methylcyclohexane D) 1-ethyl-2-methylcyclohexane E) 1-methyloctane <div style=padding-top: 35px>

A) 1-ethyl-2-methylhexane
B) 2-ethyl-1-methylcycloheptane
C) 4-ethyl-5-methylcyclohexane
D) 1-ethyl-2-methylcyclohexane
E) 1-methyloctane
Question
Which of the following correctly represents cyclopropylcyclohexane?

A)
<strong>Which of the following correctly represents cyclopropylcyclohexane?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
B)
<strong>Which of the following correctly represents cyclopropylcyclohexane?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
C)
<strong>Which of the following correctly represents cyclopropylcyclohexane?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
D)
<strong>Which of the following correctly represents cyclopropylcyclohexane?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
E) None of the above.
Question
Although five- and six-membered rings are generally the most stable,why is cyclopentane less stable than cyclohexane?

A) The angles in cyclopentane deviate significantly from the tetrahedral angle.
B) Five-membered rings have trans annular interactions.
C) Five-membered rings have eclipsing hydrogens.
D) Planar cyclohexane has bond angles closer to 109.
E) Larger rings are always more stable than smaller rings.
Question
Which of the following could have both methyl groups in an equatorial orientation?

A)
<strong>Which of the following could have both methyl groups in an equatorial orientation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which of the following could have both methyl groups in an equatorial orientation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which of the following could have both methyl groups in an equatorial orientation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which of the following could have both methyl groups in an equatorial orientation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which of the following could have both methyl groups in an equatorial orientation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following could be classified as a terpene?

A)
<strong>Which of the following could be classified as a terpene?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which of the following could be classified as a terpene?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which of the following could be classified as a terpene?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which of the following could be classified as a terpene?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which of the following could be classified as a terpene?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What would be the proper name of the following: <strong>What would be the proper name of the following:  </strong> A) cis-1-tert-butyl-4-methylcyclohexane B) trans-1-tert-butyl-4-methylcyclohexane C) axial,equatorial-1-tert-butyl-4-methylcyclohexane D) cis-1-isopropyl-4-methylcyclohexane E) trans-1-isopropyl-4-methylcyclohexane <div style=padding-top: 35px>

A) cis-1-tert-butyl-4-methylcyclohexane
B) trans-1-tert-butyl-4-methylcyclohexane
C) axial,equatorial-1-tert-butyl-4-methylcyclohexane
D) cis-1-isopropyl-4-methylcyclohexane
E) trans-1-isopropyl-4-methylcyclohexane
Question
Which of the following structures represent cis-1,4-dimethylcyclohexane? <strong>Which of the following structures represent cis-1,4-dimethylcyclohexane?  </strong> A) I & II B) I & III C) II & III D) All of the above. E) None of the above. <div style=padding-top: 35px>

A) I & II
B) I & III
C) II & III
D) All of the above.
E) None of the above.
Question
How many isoprene units are in eudesmal? <strong>How many isoprene units are in eudesmal?  </strong> A) 0 B) 1 C) 2 D) 3 E) Unable to determine <div style=padding-top: 35px>

A) 0
B) 1
C) 2
D) 3
E) Unable to determine
Question
What is the correct structure of 2-methyl-1,3-butadiene?

A)
<strong>What is the correct structure of 2-methyl-1,3-butadiene?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
B)
<strong>What is the correct structure of 2-methyl-1,3-butadiene?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
C)
<strong>What is the correct structure of 2-methyl-1,3-butadiene?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
D)
<strong>What is the correct structure of 2-methyl-1,3-butadiene?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
E) None of the above.
Question
Which conformation of cyclohexane experiences the most transannular strain?

A) Chair
B) Planar
C) Boat
D) Twist boat
E) All of these are stable.
Question
What is the most stable conformation of trans-1-fluoro-4-methylcyclohexane?

A)
<strong>What is the most stable conformation of trans-1-fluoro-4-methylcyclohexane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>What is the most stable conformation of trans-1-fluoro-4-methylcyclohexane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>What is the most stable conformation of trans-1-fluoro-4-methylcyclohexane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>What is the most stable conformation of trans-1-fluoro-4-methylcyclohexane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>What is the most stable conformation of trans-1-fluoro-4-methylcyclohexane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Steroids frequently function as _____________,which are regulators of biochemical activity.

A) proteins
B) nucleic acids
C) hormones
D) fatty acids
E) triglycerides
Question
Which of the following is not in its most stable conformation?

A)
<strong>Which of the following is not in its most stable conformation?</strong> A)   B)   C)   D)   E) All of these are in their most stable conformation. <div style=padding-top: 35px>
B)
<strong>Which of the following is not in its most stable conformation?</strong> A)   B)   C)   D)   E) All of these are in their most stable conformation. <div style=padding-top: 35px>
C)
<strong>Which of the following is not in its most stable conformation?</strong> A)   B)   C)   D)   E) All of these are in their most stable conformation. <div style=padding-top: 35px>
D)
<strong>Which of the following is not in its most stable conformation?</strong> A)   B)   C)   D)   E) All of these are in their most stable conformation. <div style=padding-top: 35px>
E) All of these are in their most stable conformation.
Question
What is the correct name for the following molecule? <strong>What is the correct name for the following molecule?  </strong> A) 1-chloro-2-methyl-4-propylcyclopentane B) 2-chloro-1-methyl-4-propylcyclopentane C) 1-chloro-5-methyl-3-propylcyclopentane D) 5-methyl-1-chloro-3-propylcylopentane E) 1-chloro-3-propyl-5-methylcyclopentane <div style=padding-top: 35px>

A) 1-chloro-2-methyl-4-propylcyclopentane
B) 2-chloro-1-methyl-4-propylcyclopentane
C) 1-chloro-5-methyl-3-propylcyclopentane
D) 5-methyl-1-chloro-3-propylcylopentane
E) 1-chloro-3-propyl-5-methylcyclopentane
Question
What is the potential energy change to convert from a twist-boat to boat conformation?

A) -14 Kcal/mol
B) 0 Kcal/mol
C) 1.4 Kcal/mol
D) 14 Kcal/mol
E) 45 Kcal/mol
Question
Cyclohexanes exhibit a higher_______than their straight-chain analogs.(Choose the correct answer)

A) boiling point
B) melting point
C) density
D) All of these are correct.
E) Two of these are correct.
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Deck 4: Cycloalkanes
1
Which of the following compounds has the highest heat of combustion per CH2 group?

A) cyclopropane
B) cyclobutane
C) cyclopentane
D) cyclohexane
E) All have equal Hcombustion.
cyclopropane
2
The most stable conformation of cis-1,3-dimethylcyclohexane has how many hydrogen atoms in axial positions?

A) 4
B) 5
C) 6
D) 8
E) None of the above.
6
3
Which of the following correctly shows the Newman projection along a C-C bond in cyclohexane? (the squiggles indicate where the rest of the ring is attached) <strong>Which of the following correctly shows the Newman projection along a C-C bond in cyclohexane? (the squiggles indicate where the rest of the ring is attached)  </strong> A) A B) B C) C D) D E) E

A) A
B) B
C) C
D) D
E) E
D
4
Which of the following statements about conformations of methylcyclohexane is true? <strong>Which of the following statements about conformations of methylcyclohexane is true?  </strong> A) The energy barrier to interconvert these is too high to be achieved at room temperature. B) The two forms are in equilibrium and are present in equal amounts at room temperature. C) The two forms are not in equilibrium but are present in equal amounts at room temperature. D) The two forms are in equilibrium but are not present in equal amounts at room temperature. E) The two forms are not in equilibrium and are not present in equal amounts at room temperature.

A) The energy barrier to interconvert these is too high to be achieved at room temperature.
B) The two forms are in equilibrium and are present in equal amounts at room temperature.
C) The two forms are not in equilibrium but are present in equal amounts at room temperature.
D) The two forms are in equilibrium but are not present in equal amounts at room temperature.
E) The two forms are not in equilibrium and are not present in equal amounts at room temperature.
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5
Which of the following isomers would you expect to have the lowest heat of combustion? (i.e.,be most stable)

A) cis-1,2-dimethylcyclohexane
B) trans-1,3-dimethylcyclohexane
C) cis-1,4-dimethylcyclohexane
D) cis-1,3-dimethylcyclohexane
E) All should have the same heat of combustion.
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6
Which of the following cyclic alkanes can be ring-opened under hydrogenation conditions? <strong>Which of the following cyclic alkanes can be ring-opened under hydrogenation conditions?  </strong> A) cyclopropane B) cyclobutane C) cyclopentane D) cyclohexane E) more than one of these

A) cyclopropane
B) cyclobutane
C) cyclopentane
D) cyclohexane
E) more than one of these
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7
Which of the following compounds has the lowest heat of combustion per CH2 group?

A) cyclopropane
B) cyclobutane
C) cyclopentane
D) cyclohexane
E) All have equal Hcombustion.
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8
Which one of the following cyclic alkanes has the greatest tendency to have a planar ring?

A) cyclopropane
B) cyclobutane
C) cyclopentane
D) cyclohexane
E) None of the above are planar.
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9
Which would be the most stable conformation of trans-1-methyl-3-isopropylcyclohexane?

A)
<strong>Which would be the most stable conformation of trans-1-methyl-3-isopropylcyclohexane?</strong> A)   B)   C)   D)   E)
B)
<strong>Which would be the most stable conformation of trans-1-methyl-3-isopropylcyclohexane?</strong> A)   B)   C)   D)   E)
C)
<strong>Which would be the most stable conformation of trans-1-methyl-3-isopropylcyclohexane?</strong> A)   B)   C)   D)   E)
D)
<strong>Which would be the most stable conformation of trans-1-methyl-3-isopropylcyclohexane?</strong> A)   B)   C)   D)   E)
E)
<strong>Which would be the most stable conformation of trans-1-methyl-3-isopropylcyclohexane?</strong> A)   B)   C)   D)   E)
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10
Which,if either,of the two isomers of the compound shown below would be more stable? <strong>Which,if either,of the two isomers of the compound shown below would be more stable?  </strong> A) Cis is more stable. B) Trans is more stable. C) Both are equally stable. D) Neither is stable. E) There is no way to predict this.

A) Cis is more stable.
B) Trans is more stable.
C) Both are equally stable.
D) Neither is stable.
E) There is no way to predict this.
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11
Which of the following disubstituted cyclohexanes could exist in a conformation that has both groups equatorial?

A) cis-1,3-dimethylcyclohexane
B) cis-1,4-dimethylcyclohexane
C) trans-1,3-dimethylcyclohexane
D) cis-1,2-dimethylcyclohexane
E) All or none can have both groups equatorial.
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12
What would be the name of the following? <strong>What would be the name of the following?  </strong> A) 5-cyclopentyl-1-methylcyclononane B) cis-1-cyclopentyl-5-methylcyclodecane C) cis-5-methyl-1-cyclopentylcyclododecane D) trans-cyclopentyl-5-methylcyclodecane E) (5-methylcyclodecyl)cyclopentane

A) 5-cyclopentyl-1-methylcyclononane
B) cis-1-cyclopentyl-5-methylcyclodecane
C) cis-5-methyl-1-cyclopentylcyclododecane
D) trans-cyclopentyl-5-methylcyclodecane
E) (5-methylcyclodecyl)cyclopentane
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13
Terpenes can be considered to be built up from what units?

A)
<strong>Terpenes can be considered to be built up from what units?</strong> A)   B)   C)   D)   E)
B)
<strong>Terpenes can be considered to be built up from what units?</strong> A)   B)   C)   D)   E)
C)
<strong>Terpenes can be considered to be built up from what units?</strong> A)   B)   C)   D)   E)
D)
<strong>Terpenes can be considered to be built up from what units?</strong> A)   B)   C)   D)   E)
E)
<strong>Terpenes can be considered to be built up from what units?</strong> A)   B)   C)   D)   E)
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14
Which of the following ring systems belongs to the class of compounds called steroids?

A)
<strong>Which of the following ring systems belongs to the class of compounds called steroids?</strong> A)   B)   C)   D)   E)
B)
<strong>Which of the following ring systems belongs to the class of compounds called steroids?</strong> A)   B)   C)   D)   E)
C)
<strong>Which of the following ring systems belongs to the class of compounds called steroids?</strong> A)   B)   C)   D)   E)
D)
<strong>Which of the following ring systems belongs to the class of compounds called steroids?</strong> A)   B)   C)   D)   E)
E)
<strong>Which of the following ring systems belongs to the class of compounds called steroids?</strong> A)   B)   C)   D)   E)
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15
What is the correct IUPAC name for the following molecule: <strong>What is the correct IUPAC name for the following molecule:  </strong> A) 1-ethyl-2-methylhexane B) 2-ethyl-1-methylcycloheptane C) 4-ethyl-5-methylcyclohexane D) 1-ethyl-2-methylcyclohexane E) 1-methyloctane

A) 1-ethyl-2-methylhexane
B) 2-ethyl-1-methylcycloheptane
C) 4-ethyl-5-methylcyclohexane
D) 1-ethyl-2-methylcyclohexane
E) 1-methyloctane
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16
Which of the following correctly represents cyclopropylcyclohexane?

A)
<strong>Which of the following correctly represents cyclopropylcyclohexane?</strong> A)   B)   C)   D)   E) None of the above.
B)
<strong>Which of the following correctly represents cyclopropylcyclohexane?</strong> A)   B)   C)   D)   E) None of the above.
C)
<strong>Which of the following correctly represents cyclopropylcyclohexane?</strong> A)   B)   C)   D)   E) None of the above.
D)
<strong>Which of the following correctly represents cyclopropylcyclohexane?</strong> A)   B)   C)   D)   E) None of the above.
E) None of the above.
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17
Although five- and six-membered rings are generally the most stable,why is cyclopentane less stable than cyclohexane?

A) The angles in cyclopentane deviate significantly from the tetrahedral angle.
B) Five-membered rings have trans annular interactions.
C) Five-membered rings have eclipsing hydrogens.
D) Planar cyclohexane has bond angles closer to 109.
E) Larger rings are always more stable than smaller rings.
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18
Which of the following could have both methyl groups in an equatorial orientation?

A)
<strong>Which of the following could have both methyl groups in an equatorial orientation?</strong> A)   B)   C)   D)   E)
B)
<strong>Which of the following could have both methyl groups in an equatorial orientation?</strong> A)   B)   C)   D)   E)
C)
<strong>Which of the following could have both methyl groups in an equatorial orientation?</strong> A)   B)   C)   D)   E)
D)
<strong>Which of the following could have both methyl groups in an equatorial orientation?</strong> A)   B)   C)   D)   E)
E)
<strong>Which of the following could have both methyl groups in an equatorial orientation?</strong> A)   B)   C)   D)   E)
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19
Which of the following could be classified as a terpene?

A)
<strong>Which of the following could be classified as a terpene?</strong> A)   B)   C)   D)   E)
B)
<strong>Which of the following could be classified as a terpene?</strong> A)   B)   C)   D)   E)
C)
<strong>Which of the following could be classified as a terpene?</strong> A)   B)   C)   D)   E)
D)
<strong>Which of the following could be classified as a terpene?</strong> A)   B)   C)   D)   E)
E)
<strong>Which of the following could be classified as a terpene?</strong> A)   B)   C)   D)   E)
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20
What would be the proper name of the following: <strong>What would be the proper name of the following:  </strong> A) cis-1-tert-butyl-4-methylcyclohexane B) trans-1-tert-butyl-4-methylcyclohexane C) axial,equatorial-1-tert-butyl-4-methylcyclohexane D) cis-1-isopropyl-4-methylcyclohexane E) trans-1-isopropyl-4-methylcyclohexane

A) cis-1-tert-butyl-4-methylcyclohexane
B) trans-1-tert-butyl-4-methylcyclohexane
C) axial,equatorial-1-tert-butyl-4-methylcyclohexane
D) cis-1-isopropyl-4-methylcyclohexane
E) trans-1-isopropyl-4-methylcyclohexane
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21
Which of the following structures represent cis-1,4-dimethylcyclohexane? <strong>Which of the following structures represent cis-1,4-dimethylcyclohexane?  </strong> A) I & II B) I & III C) II & III D) All of the above. E) None of the above.

A) I & II
B) I & III
C) II & III
D) All of the above.
E) None of the above.
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22
How many isoprene units are in eudesmal? <strong>How many isoprene units are in eudesmal?  </strong> A) 0 B) 1 C) 2 D) 3 E) Unable to determine

A) 0
B) 1
C) 2
D) 3
E) Unable to determine
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23
What is the correct structure of 2-methyl-1,3-butadiene?

A)
<strong>What is the correct structure of 2-methyl-1,3-butadiene?</strong> A)   B)   C)   D)   E) None of the above.
B)
<strong>What is the correct structure of 2-methyl-1,3-butadiene?</strong> A)   B)   C)   D)   E) None of the above.
C)
<strong>What is the correct structure of 2-methyl-1,3-butadiene?</strong> A)   B)   C)   D)   E) None of the above.
D)
<strong>What is the correct structure of 2-methyl-1,3-butadiene?</strong> A)   B)   C)   D)   E) None of the above.
E) None of the above.
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24
Which conformation of cyclohexane experiences the most transannular strain?

A) Chair
B) Planar
C) Boat
D) Twist boat
E) All of these are stable.
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25
What is the most stable conformation of trans-1-fluoro-4-methylcyclohexane?

A)
<strong>What is the most stable conformation of trans-1-fluoro-4-methylcyclohexane?</strong> A)   B)   C)   D)   E)
B)
<strong>What is the most stable conformation of trans-1-fluoro-4-methylcyclohexane?</strong> A)   B)   C)   D)   E)
C)
<strong>What is the most stable conformation of trans-1-fluoro-4-methylcyclohexane?</strong> A)   B)   C)   D)   E)
D)
<strong>What is the most stable conformation of trans-1-fluoro-4-methylcyclohexane?</strong> A)   B)   C)   D)   E)
E)
<strong>What is the most stable conformation of trans-1-fluoro-4-methylcyclohexane?</strong> A)   B)   C)   D)   E)
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26
Steroids frequently function as _____________,which are regulators of biochemical activity.

A) proteins
B) nucleic acids
C) hormones
D) fatty acids
E) triglycerides
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27
Which of the following is not in its most stable conformation?

A)
<strong>Which of the following is not in its most stable conformation?</strong> A)   B)   C)   D)   E) All of these are in their most stable conformation.
B)
<strong>Which of the following is not in its most stable conformation?</strong> A)   B)   C)   D)   E) All of these are in their most stable conformation.
C)
<strong>Which of the following is not in its most stable conformation?</strong> A)   B)   C)   D)   E) All of these are in their most stable conformation.
D)
<strong>Which of the following is not in its most stable conformation?</strong> A)   B)   C)   D)   E) All of these are in their most stable conformation.
E) All of these are in their most stable conformation.
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28
What is the correct name for the following molecule? <strong>What is the correct name for the following molecule?  </strong> A) 1-chloro-2-methyl-4-propylcyclopentane B) 2-chloro-1-methyl-4-propylcyclopentane C) 1-chloro-5-methyl-3-propylcyclopentane D) 5-methyl-1-chloro-3-propylcylopentane E) 1-chloro-3-propyl-5-methylcyclopentane

A) 1-chloro-2-methyl-4-propylcyclopentane
B) 2-chloro-1-methyl-4-propylcyclopentane
C) 1-chloro-5-methyl-3-propylcyclopentane
D) 5-methyl-1-chloro-3-propylcylopentane
E) 1-chloro-3-propyl-5-methylcyclopentane
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29
What is the potential energy change to convert from a twist-boat to boat conformation?

A) -14 Kcal/mol
B) 0 Kcal/mol
C) 1.4 Kcal/mol
D) 14 Kcal/mol
E) 45 Kcal/mol
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30
Cyclohexanes exhibit a higher_______than their straight-chain analogs.(Choose the correct answer)

A) boiling point
B) melting point
C) density
D) All of these are correct.
E) Two of these are correct.
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