Deck 4: Alkanes: Nomenclature, Conformational Analysis, and an Introduction to Synthesis
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Deck 4: Alkanes: Nomenclature, Conformational Analysis, and an Introduction to Synthesis
1
An IUPAC name for
is:
A) 3-Isobutyl-2,4-dimethylhexane
B) 3-sec-Butyl-2,5-dimethylhexane
C) 4-sec-Butyl-2,5-dimethylhexane
D) 4-Isopropyl-2,5-dimethylheptane
E) 4-Isopropyl-3,6-dimethylheptane

A) 3-Isobutyl-2,4-dimethylhexane
B) 3-sec-Butyl-2,5-dimethylhexane
C) 4-sec-Butyl-2,5-dimethylhexane
D) 4-Isopropyl-2,5-dimethylheptane
E) 4-Isopropyl-3,6-dimethylheptane
4-Isopropyl-2,5-dimethylheptane
2
Which of these is the common name for the 1,1-dimethylpropyl group?
A) tert-Butyl
B) tert-Pentyl
C) Isopentyl
D) Neopentyl
E) sec-Pentyl
A) tert-Butyl
B) tert-Pentyl
C) Isopentyl
D) Neopentyl
E) sec-Pentyl
tert-Pentyl
3
A correct IUPAC name for the following compound is: 
A) 2,5-Dimethyl-3-propylheptane
B) 3,6-Dimethyl-5-propylheptane
C) 6-Methyl-4-(1-methylethyl)octane
D) 2-Methyl-3-(2-methylbutyl)hexane
E) 3-Methyl-5-(1-methylethyl)octane

A) 2,5-Dimethyl-3-propylheptane
B) 3,6-Dimethyl-5-propylheptane
C) 6-Methyl-4-(1-methylethyl)octane
D) 2-Methyl-3-(2-methylbutyl)hexane
E) 3-Methyl-5-(1-methylethyl)octane
3-Methyl-5-(1-methylethyl)octane
4
What is the correct IUPAC name for the following compound? 
A) 3-Hydroxymethylheptane
B) 3-Hydroxymethylhexane
C) 3-Methyloxyheptane
D) 2-Ethyl-1-hexanol
E) 2-Ethyl-1-heptanol

A) 3-Hydroxymethylheptane
B) 3-Hydroxymethylhexane
C) 3-Methyloxyheptane
D) 2-Ethyl-1-hexanol
E) 2-Ethyl-1-heptanol
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5
How many compounds with the formula C7H16 (heptanes)contain a single 3° carbon atom?
A) 2
B) 3
C) 4
D) 5
E) 6
A) 2
B) 3
C) 4
D) 5
E) 6
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6
What is the simplest alkane,i.e. ,the one with the smallest molecular weight,which possesses primary,secondary and tertiary carbon atoms?
A) 2-Methylpropane
B) 2-Methylbutane
C) 2-Methylpentane
D) 3-Methylpentane
E) 2,2-Dimethylbutane
A) 2-Methylpropane
B) 2-Methylbutane
C) 2-Methylpentane
D) 3-Methylpentane
E) 2,2-Dimethylbutane
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7
Which of the following pairs of compounds represent pairs of constitutional isomers?
A) 2-Methylbutane and pentane
B) 2-Chlorohexane and 3-chlorohexane
C) sec-Butyl bromide and tert-butyl bromide
D) Propyl chloride and isopropyl chloride
E) All of the above
A) 2-Methylbutane and pentane
B) 2-Chlorohexane and 3-chlorohexane
C) sec-Butyl bromide and tert-butyl bromide
D) Propyl chloride and isopropyl chloride
E) All of the above
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8
The neopentyl group has the alternative name:
A) 1,1-Dimethylpropyl
B) 1,2-Dimethylpropyl
C) 2,2-Dimethylpropyl
D) 1-Methylbutyl
E) 2-Methylbutyl
A) 1,1-Dimethylpropyl
B) 1,2-Dimethylpropyl
C) 2,2-Dimethylpropyl
D) 1-Methylbutyl
E) 2-Methylbutyl
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9
What is the common name for this compound? 
A) Isobutyl bromide
B) tert-Butyl bromide
C) Butyl bromide
D) sec-Butyl bromide
E) Bromo-sec-butane

A) Isobutyl bromide
B) tert-Butyl bromide
C) Butyl bromide
D) sec-Butyl bromide
E) Bromo-sec-butane
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10
What is the correct IUPAC name for the following compound? 
A) 5-Ethyl-3-methylhexanol
B) 5-Ethyl-3-methyl-1-hexanol
C) 2-Ethyl-4-methyl-6-hexanol
D) 3,5-Dimethyl-7-heptanol
E) 3,5-Dimethyl-1-heptanol

A) 5-Ethyl-3-methylhexanol
B) 5-Ethyl-3-methyl-1-hexanol
C) 2-Ethyl-4-methyl-6-hexanol
D) 3,5-Dimethyl-7-heptanol
E) 3,5-Dimethyl-1-heptanol
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11
How many alkanes of formula C7H16 possess a quaternary carbon atom?
A) 1
B) 2
C) 3
D) 4
E) 5
A) 1
B) 2
C) 3
D) 4
E) 5
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12
An IUPAC name for the group
is:
A) Isopentyl
B) Isoamyl
C) sec-Butylmethyl
D) 2-Methylbutyl
E) 2-Ethylpropyl

A) Isopentyl
B) Isoamyl
C) sec-Butylmethyl
D) 2-Methylbutyl
E) 2-Ethylpropyl
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13
The correct IUPAC name for
is:
A) 2-Bromo-4-chloro-4-isopropylpentane
B) 4-Bromo-2-chloro-2-isopropylpentane
C) 5-Bromo-3-chloro-2,3-dimethylhexane
D) 2-Bromo-4-chloro-4,5-dimethylhexane
E) 2-(2-Bromopropyl)-2-chloro-3-methylbutane

A) 2-Bromo-4-chloro-4-isopropylpentane
B) 4-Bromo-2-chloro-2-isopropylpentane
C) 5-Bromo-3-chloro-2,3-dimethylhexane
D) 2-Bromo-4-chloro-4,5-dimethylhexane
E) 2-(2-Bromopropyl)-2-chloro-3-methylbutane
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14
How many constitutional isomers are possible for the formula C6H14?
A) 2
B) 3
C) 4
D) 5
E) 6
A) 2
B) 3
C) 4
D) 5
E) 6
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15
An IUPAC name for
is:
A) 5-Methyl-4-(1-methylpropyl)hexane
B) 2-Methyl-3-(1-methylpropyl)hexane
C) 2-Methyl-3-(2-methylpropyl)hexane
D) 3-Methyl-4-(1-methylethyl)heptane
E) 5-Methyl-4-(1-methylethyl)heptane

A) 5-Methyl-4-(1-methylpropyl)hexane
B) 2-Methyl-3-(1-methylpropyl)hexane
C) 2-Methyl-3-(2-methylpropyl)hexane
D) 3-Methyl-4-(1-methylethyl)heptane
E) 5-Methyl-4-(1-methylethyl)heptane
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16
An IUPAC name for the following compound is: 
A) 4-Isobutyl-3,4-dimethylheptane
B) 4-sec-Butyl-2,4-dimethylheptane
C) 2,4,5-Trimethyl-4-propylheptane
D) 3,4,6-Trimethyl-4-propylheptane
E) 4-Isobutyl-4,5-dimethylheptane

A) 4-Isobutyl-3,4-dimethylheptane
B) 4-sec-Butyl-2,4-dimethylheptane
C) 2,4,5-Trimethyl-4-propylheptane
D) 3,4,6-Trimethyl-4-propylheptane
E) 4-Isobutyl-4,5-dimethylheptane
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17
What is a correct name for the following compound? 
A) 3-Isobutyl-2-methylheptane
B) 3-sec-Butyl-2-methyloctane
C) 5-Isobutyl-6-methylheptane
D) 2-Ethyl-3-isopropyloctane
E) 4-Isopropyl-3-methylnonane

A) 3-Isobutyl-2-methylheptane
B) 3-sec-Butyl-2-methyloctane
C) 5-Isobutyl-6-methylheptane
D) 2-Ethyl-3-isopropyloctane
E) 4-Isopropyl-3-methylnonane
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18
Isopentyl is the common name for which alkyl group?
A)

B)

C)

D)

E)

A)

B)

C)

D)

E)

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19
The IUPAC name for
is:
A) 6-Ethyl-3,4-dimethylheptane
B) 2-Ethyl-4,5-dimethylheptane
C) 3,4,6-Trimethyloctane
D) 3,5,6-Trimethyloctane
E) 2-(1-Methylpropyl)-4-methylhexane

A) 6-Ethyl-3,4-dimethylheptane
B) 2-Ethyl-4,5-dimethylheptane
C) 3,4,6-Trimethyloctane
D) 3,5,6-Trimethyloctane
E) 2-(1-Methylpropyl)-4-methylhexane
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20
Neglecting stereochemistry,which of these common group names is ambiguous,i.e. ,does not refer to one specific group?
A) Butyl
B) sec-Butyl
C) tert-Pentyl
D) Neopentyl
E) sec-Pentyl
A) Butyl
B) sec-Butyl
C) tert-Pentyl
D) Neopentyl
E) sec-Pentyl
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21
Which is the correct name for the compound shown below? ![<strong>Which is the correct name for the compound shown below? </strong> A) Bicyclo[2.2.0]hexane B) Bicyclo[2.2.0]butane C) Bicyclo[2.2.2]hexane D) Bicyclo[2.2.1]hexane E) Disquarane](https://storage.examlex.com/TB5901/11ea9a02_1a9b_7846_8bb6_450e40306776_TB5901_00.jpg)
A) Bicyclo[2.2.0]hexane
B) Bicyclo[2.2.0]butane
C) Bicyclo[2.2.2]hexane
D) Bicyclo[2.2.1]hexane
E) Disquarane
![<strong>Which is the correct name for the compound shown below? </strong> A) Bicyclo[2.2.0]hexane B) Bicyclo[2.2.0]butane C) Bicyclo[2.2.2]hexane D) Bicyclo[2.2.1]hexane E) Disquarane](https://storage.examlex.com/TB5901/11ea9a02_1a9b_7846_8bb6_450e40306776_TB5901_00.jpg)
A) Bicyclo[2.2.0]hexane
B) Bicyclo[2.2.0]butane
C) Bicyclo[2.2.2]hexane
D) Bicyclo[2.2.1]hexane
E) Disquarane
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22
A correct name for the following compound is: ![<strong>A correct name for the following compound is: </strong> A) 3-chloro-8-methylbicyclo[4.3.0]nonane B) 8-Methyl-3-chlorobicyclo[4.3.1]nonane C) 3-Methyl-7-chlorobicyclo[4.3.0]nonane D) 3-Methyl-7-chlorobicyclo[4.3.1]decane E) 3-chloro-8-methyl[4.3.0]bicyclononane](https://storage.examlex.com/TB5901/11ea9a02_1a9c_89be_8bb6_770f0421f696_TB5901_00.jpg)
A) 3-chloro-8-methylbicyclo[4.3.0]nonane
B) 8-Methyl-3-chlorobicyclo[4.3.1]nonane
C) 3-Methyl-7-chlorobicyclo[4.3.0]nonane
D) 3-Methyl-7-chlorobicyclo[4.3.1]decane
E) 3-chloro-8-methyl[4.3.0]bicyclononane
![<strong>A correct name for the following compound is: </strong> A) 3-chloro-8-methylbicyclo[4.3.0]nonane B) 8-Methyl-3-chlorobicyclo[4.3.1]nonane C) 3-Methyl-7-chlorobicyclo[4.3.0]nonane D) 3-Methyl-7-chlorobicyclo[4.3.1]decane E) 3-chloro-8-methyl[4.3.0]bicyclononane](https://storage.examlex.com/TB5901/11ea9a02_1a9c_89be_8bb6_770f0421f696_TB5901_00.jpg)
A) 3-chloro-8-methylbicyclo[4.3.0]nonane
B) 8-Methyl-3-chlorobicyclo[4.3.1]nonane
C) 3-Methyl-7-chlorobicyclo[4.3.0]nonane
D) 3-Methyl-7-chlorobicyclo[4.3.1]decane
E) 3-chloro-8-methyl[4.3.0]bicyclononane
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23
The most stable conformation of 2,3-dimethylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back): 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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24
The least stable conformation of 2,3-dimethylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back): 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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25
Which compound is a bicycloheptane? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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26
The most stable conformation of 3-bromo-2-methylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back): 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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27
What is the correct name of the following compound? ![<strong>What is the correct name of the following compound? </strong> A) 1-Chlorobicyclo[4.1.1]octane B) 2-Chlorobicyclo[4.1.0]octane C) 2-Chlorobicyclo[4.1.1]octane D) 2-Chlorobicyclo[4.1.1]heptane E) 5-Chlorobicyclo[4.1.1]octane](https://storage.examlex.com/TB5901/11ea9a02_1a9c_62ad_8bb6_3bf9180c9667_TB5901_00.jpg)
A) 1-Chlorobicyclo[4.1.1]octane
B) 2-Chlorobicyclo[4.1.0]octane
C) 2-Chlorobicyclo[4.1.1]octane
D) 2-Chlorobicyclo[4.1.1]heptane
E) 5-Chlorobicyclo[4.1.1]octane
![<strong>What is the correct name of the following compound? </strong> A) 1-Chlorobicyclo[4.1.1]octane B) 2-Chlorobicyclo[4.1.0]octane C) 2-Chlorobicyclo[4.1.1]octane D) 2-Chlorobicyclo[4.1.1]heptane E) 5-Chlorobicyclo[4.1.1]octane](https://storage.examlex.com/TB5901/11ea9a02_1a9c_62ad_8bb6_3bf9180c9667_TB5901_00.jpg)
A) 1-Chlorobicyclo[4.1.1]octane
B) 2-Chlorobicyclo[4.1.0]octane
C) 2-Chlorobicyclo[4.1.1]octane
D) 2-Chlorobicyclo[4.1.1]heptane
E) 5-Chlorobicyclo[4.1.1]octane
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28
![<strong> Which of the above is bicyclo[4.3.0]nonane?</strong> A) I B) II C) III D) IV E) V](https://storage.examlex.com/TB5901/11ea9a02_1a9b_ed7a_8bb6_335ed14b7a25_TB5901_00.jpg)
Which of the above is bicyclo[4.3.0]nonane?
A) I
B) II
C) III
D) IV
E) V
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29
What is the name of this compound? ![<strong>What is the name of this compound? </strong> A) Bicyclo[2.2.2]octane B) Bicyclo[3.2.1]octane C) Bicyclo[4.1.1]octane D) Bicyclo[4.2.0]octane E) Bicyclo[3.3.0]octane](https://storage.examlex.com/TB5901/11ea9a02_1a9b_7847_8bb6_974cc9d67f52_TB5901_00.jpg)
A) Bicyclo[2.2.2]octane
B) Bicyclo[3.2.1]octane
C) Bicyclo[4.1.1]octane
D) Bicyclo[4.2.0]octane
E) Bicyclo[3.3.0]octane
![<strong>What is the name of this compound? </strong> A) Bicyclo[2.2.2]octane B) Bicyclo[3.2.1]octane C) Bicyclo[4.1.1]octane D) Bicyclo[4.2.0]octane E) Bicyclo[3.3.0]octane](https://storage.examlex.com/TB5901/11ea9a02_1a9b_7847_8bb6_974cc9d67f52_TB5901_00.jpg)
A) Bicyclo[2.2.2]octane
B) Bicyclo[3.2.1]octane
C) Bicyclo[4.1.1]octane
D) Bicyclo[4.2.0]octane
E) Bicyclo[3.3.0]octane
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30
Which of the following is bicyclo[3.2.2]nonane? ![<strong>Which of the following is bicyclo[3.2.2]nonane? </strong> A) I B) II C) III D) IV E) V](https://storage.examlex.com/TB5901/11ea9a02_1a9b_2a24_8bb6_598295075a00_TB5901_00.jpg)
A) I
B) II
C) III
D) IV
E) V
![<strong>Which of the following is bicyclo[3.2.2]nonane? </strong> A) I B) II C) III D) IV E) V](https://storage.examlex.com/TB5901/11ea9a02_1a9b_2a24_8bb6_598295075a00_TB5901_00.jpg)
A) I
B) II
C) III
D) IV
E) V
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31
Which of the following is a correct name which corresponds to the common name tert-pentyl alcohol?
A) 2,2-Dimethyl-1-propanol
B) 2-Ethyl-2-propanol
C) 2-Methyl-2-butanol
D) 3-Methyl-1-butanol
E) Methyl tert-butanol
A) 2,2-Dimethyl-1-propanol
B) 2-Ethyl-2-propanol
C) 2-Methyl-2-butanol
D) 3-Methyl-1-butanol
E) Methyl tert-butanol
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32
The correct IUPAC name for the following compound is: 
A) 1-Hydroxy-3-sec-butylcyclopentane
B) 3-sec-Butyl-1-cyclopentanol
C) 1-sec-Butyl-3-cyclopentanol
D) 4-sec-Butyl-1-cyclopentanol
E) 3-Isobutyl-1-cyclopentanol

A) 1-Hydroxy-3-sec-butylcyclopentane
B) 3-sec-Butyl-1-cyclopentanol
C) 1-sec-Butyl-3-cyclopentanol
D) 4-sec-Butyl-1-cyclopentanol
E) 3-Isobutyl-1-cyclopentanol
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33
A correct name for the following compound is: ![<strong>A correct name for the following compound is: </strong> A) 4-bromo-3,8-dimethylbicyclo[5.2.2]nonane B) 3,8-dimethyl-4-bromo-bicyclo[5.2.0]nonane C) 4-bromo-3,8-dimethylbicyclo[5.2.1]decane D) 7-bromo-2,6-dimethylbicyclo[5.2.0]nonane E) 4-bromo-3,8-dimethylbicyclo[5.2.0]nonane](https://storage.examlex.com/TB5901/11ea9a02_1a9c_b0cf_8bb6_41e054efb335_TB5901_00.jpg)
A) 4-bromo-3,8-dimethylbicyclo[5.2.2]nonane
B) 3,8-dimethyl-4-bromo-bicyclo[5.2.0]nonane
C) 4-bromo-3,8-dimethylbicyclo[5.2.1]decane
D) 7-bromo-2,6-dimethylbicyclo[5.2.0]nonane
E) 4-bromo-3,8-dimethylbicyclo[5.2.0]nonane
![<strong>A correct name for the following compound is: </strong> A) 4-bromo-3,8-dimethylbicyclo[5.2.2]nonane B) 3,8-dimethyl-4-bromo-bicyclo[5.2.0]nonane C) 4-bromo-3,8-dimethylbicyclo[5.2.1]decane D) 7-bromo-2,6-dimethylbicyclo[5.2.0]nonane E) 4-bromo-3,8-dimethylbicyclo[5.2.0]nonane](https://storage.examlex.com/TB5901/11ea9a02_1a9c_b0cf_8bb6_41e054efb335_TB5901_00.jpg)
A) 4-bromo-3,8-dimethylbicyclo[5.2.2]nonane
B) 3,8-dimethyl-4-bromo-bicyclo[5.2.0]nonane
C) 4-bromo-3,8-dimethylbicyclo[5.2.1]decane
D) 7-bromo-2,6-dimethylbicyclo[5.2.0]nonane
E) 4-bromo-3,8-dimethylbicyclo[5.2.0]nonane
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34
What is the correct IUPAC name for the following compound? 
A) 5-Ethyl-3-fluorohexanol
B) 5-Ethyl-3-fluoro-1-hexanol
C) 2-Ethyl-4-fluoro-6-hexanol
D) 3-fluoro-5-methyl-7-heptanol
E) 3-fluoro-5-methyl-1-heptanol

A) 5-Ethyl-3-fluorohexanol
B) 5-Ethyl-3-fluoro-1-hexanol
C) 2-Ethyl-4-fluoro-6-hexanol
D) 3-fluoro-5-methyl-7-heptanol
E) 3-fluoro-5-methyl-1-heptanol
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35
A correct IUPAC name for the following compound is: 
A) 4-propyl-5-chloro-3-heptanol
B) 4-propyl-3-chloro-5-heptanol
C) 4-(1-chloropropyl)-3-heptanol
D) 5-chloro-4-propyl-3-heptanol
E) 3-hydroxy-4-propyl-5-chloroheptane

A) 4-propyl-5-chloro-3-heptanol
B) 4-propyl-3-chloro-5-heptanol
C) 4-(1-chloropropyl)-3-heptanol
D) 5-chloro-4-propyl-3-heptanol
E) 3-hydroxy-4-propyl-5-chloroheptane
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36
A correct name for the following compound is: ![<strong>A correct name for the following compound is: </strong> A) 2-Methylbicyclo[4.3.0]nonane B) 1-Methylbicyclo[4.3.1]nonane C) 7-Methylbicyclo[4.3.0]nonane D) 2-Methylbicyclo[4.3.1]nonane E) 1-Methylbicyclo[4.3.0]nonane](https://storage.examlex.com/TB5901/11ea9a02_1a9c_3b9c_8bb6_813e3c567af6_TB5901_00.jpg)
A) 2-Methylbicyclo[4.3.0]nonane
B) 1-Methylbicyclo[4.3.1]nonane
C) 7-Methylbicyclo[4.3.0]nonane
D) 2-Methylbicyclo[4.3.1]nonane
E) 1-Methylbicyclo[4.3.0]nonane
![<strong>A correct name for the following compound is: </strong> A) 2-Methylbicyclo[4.3.0]nonane B) 1-Methylbicyclo[4.3.1]nonane C) 7-Methylbicyclo[4.3.0]nonane D) 2-Methylbicyclo[4.3.1]nonane E) 1-Methylbicyclo[4.3.0]nonane](https://storage.examlex.com/TB5901/11ea9a02_1a9c_3b9c_8bb6_813e3c567af6_TB5901_00.jpg)
A) 2-Methylbicyclo[4.3.0]nonane
B) 1-Methylbicyclo[4.3.1]nonane
C) 7-Methylbicyclo[4.3.0]nonane
D) 2-Methylbicyclo[4.3.1]nonane
E) 1-Methylbicyclo[4.3.0]nonane
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37
![<strong> Which of the above is bicyclo[3.3.1]nonane?</strong> A) I B) II C) III D) IV E) V](https://storage.examlex.com/TB5901/11ea9a02_1a9b_9f58_8bb6_b514fd5d0118_TB5901_00.jpg)
Which of the above is bicyclo[3.3.1]nonane?
A) I
B) II
C) III
D) IV
E) V
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38
Which of the following structures represents bicyclo[3.2.1]octane? ![<strong>Which of the following structures represents bicyclo[3.2.1]octane? </strong> A) I B) II C) III D) IV E) V](https://storage.examlex.com/TB5901/11ea9a02_1a9c_148b_8bb6_e94b9757f73a_TB5901_00.jpg)
A) I
B) II
C) III
D) IV
E) V
![<strong>Which of the following structures represents bicyclo[3.2.1]octane? </strong> A) I B) II C) III D) IV E) V](https://storage.examlex.com/TB5901/11ea9a02_1a9c_148b_8bb6_e94b9757f73a_TB5901_00.jpg)
A) I
B) II
C) III
D) IV
E) V
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39
![<strong> Which of the above is bicyclo[5.2.0]nonane?</strong> A) I B) II C) III D) IV E) V](https://storage.examlex.com/TB5901/11ea9a02_1a9b_c669_8bb6_d1b95426b0ec_TB5901_00.jpg)
Which of the above is bicyclo[5.2.0]nonane?
A) I
B) II
C) III
D) IV
E) V
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40
The least stable conformation of 3-bromo-2-methylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back): 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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41
Select the systematic name for 
A) cis-1,3-Dichlorocyclopentane
B) trans-1,4-Dichlorocyclopentane
C) cis-1,2-Dichlorocyclopentane
D) trans-1,3-Dichlorocyclopentane
E) 1,1-Dichlorocyclopentane

A) cis-1,3-Dichlorocyclopentane
B) trans-1,4-Dichlorocyclopentane
C) cis-1,2-Dichlorocyclopentane
D) trans-1,3-Dichlorocyclopentane
E) 1,1-Dichlorocyclopentane
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42
Consider the graph below,which is a plot of the relative energies of the various conformations of hexane,viewed through the C-2-C-3 bond.The conformations corresponding to the 60o and 300o are: 
A) Eclipsed
B) Staggered and gauche
C) Staggered and anti
D) More stable than the conformation at 180o
E) None of the above

A) Eclipsed
B) Staggered and gauche
C) Staggered and anti
D) More stable than the conformation at 180o
E) None of the above
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43
The least stable conformation of 3-bromo-2-methylpentane,viewed through the C-3-C-4 bond (i.e. ,C-3 in the front,C-4 in the back): 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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44
Which conformation(s)of 1,2-dibromoethane does not illustrate one or more gauche interactions? 
A) I and II only
B) II,III,and V only
C) I,III,and IV only
D) All but one above
E) All the above

A) I and II only
B) II,III,and V only
C) I,III,and IV only
D) All but one above
E) All the above
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45
The most stable conformation of 3-bromo-2-methylpentane,viewed through the C-3-C-4 bond (i.e. ,C-3 in the front,C-4 in the back): 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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46
Which is the most stable conformation of cyclohexane?
A) Chair
B) Twist
C) Boat
D) One-half chair
E) Staggered
A) Chair
B) Twist
C) Boat
D) One-half chair
E) Staggered
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47
Consider the graph below,which is a plot of the relative energies of the various conformations of 2,3-dimethylbutane,viewed through the C-2-C-3 bond.The conformations corresponding to the 120o and 240o are: 
A) Eclipsed,more stable than the conformation at 0o
B) Eclipsed,more stable than the conformation at 180o
C) Staggered,more stable than the conformation at 0o
D) Staggered,less stable than the conformation at 180o
E) Two of the above are true

A) Eclipsed,more stable than the conformation at 0o
B) Eclipsed,more stable than the conformation at 180o
C) Staggered,more stable than the conformation at 0o
D) Staggered,less stable than the conformation at 180o
E) Two of the above are true
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48
The most stable conformation for 1,2-ethanediol (ethylene glycol)is shown below.It is the most stable conformation because: 
A) this corresponds to an anti conformation.
B) in general,gauche conformations possess the minimum energy.
C) it is stabilized by intramolecular hydrogen bonding.
D) it is a staggered conformation.
E) it has the highest energy of all the possibilities.

A) this corresponds to an anti conformation.
B) in general,gauche conformations possess the minimum energy.
C) it is stabilized by intramolecular hydrogen bonding.
D) it is a staggered conformation.
E) it has the highest energy of all the possibilities.
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49
The most stable conformation of butane is: 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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50
Give the IUPAC name for 
A) 3-Methyl-4-hexyne
B) 4-Methyl-2-hexyne
C) 2-Ethyl-3-pentyne
D) 4-Ethyl-2-pentyne
E) 3-Methyl-2-hexyne

A) 3-Methyl-4-hexyne
B) 4-Methyl-2-hexyne
C) 2-Ethyl-3-pentyne
D) 4-Ethyl-2-pentyne
E) 3-Methyl-2-hexyne
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51
The least stable conformation of butane is: 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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52
The most stable conformation of 1,2-dibromoethane is: 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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53
The graph below is a plot of the relative energies of the various conformations of: 
A) 2-chloropropane
B) 1,3-dichloropropane
C) 2-methylpropane
D) Butane (C1-C2 rotation)
E) Butane (C2-C3 rotation)

A) 2-chloropropane
B) 1,3-dichloropropane
C) 2-methylpropane
D) Butane (C1-C2 rotation)
E) Butane (C2-C3 rotation)
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54
The IUPAC name for diisobutylacetylene is
A) 2,7-Dimethyl-4-octene
B) 2,7-Dimethyl-4-octyne
C) 3,6-Dimethyl-4-octyne
D) 2,5-Diethyl-3-hexyne
E) 2,2,5,5-Tetramethyl-3-hexyne
A) 2,7-Dimethyl-4-octene
B) 2,7-Dimethyl-4-octyne
C) 3,6-Dimethyl-4-octyne
D) 2,5-Diethyl-3-hexyne
E) 2,2,5,5-Tetramethyl-3-hexyne
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55
A correct IUPAC name for the following compound is: 
A) 3,6,7-trimethyl-4-bromo-1-octene
B) 4-bromo-3-methyl-6-isopropyl-1-heptene
C) 4-bromo-3,6,7-trimethyl-1-octene
D) 4-bromo-6-isopropyl-3-methyl-1-heptene
E) 4-bromo-6-isopropyl-3,6-dimethyl-1-hexene

A) 3,6,7-trimethyl-4-bromo-1-octene
B) 4-bromo-3-methyl-6-isopropyl-1-heptene
C) 4-bromo-3,6,7-trimethyl-1-octene
D) 4-bromo-6-isopropyl-3-methyl-1-heptene
E) 4-bromo-6-isopropyl-3,6-dimethyl-1-hexene
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56
What is the correct IUPAC name for the following compound? 
A) trans-3-Hydroxymethyl-2-heptene
B) trans-2-(1-methylethyl)-4-hexen-1-ol
C) trans-5-(1-methylethyl)-2-hexen-6-ol
D) cis-5-isopropyl-2,6-hexenol
E) cis-2-(1-methylethyl)-4-hepten-1-ol

A) trans-3-Hydroxymethyl-2-heptene
B) trans-2-(1-methylethyl)-4-hexen-1-ol
C) trans-5-(1-methylethyl)-2-hexen-6-ol
D) cis-5-isopropyl-2,6-hexenol
E) cis-2-(1-methylethyl)-4-hepten-1-ol
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57
Which cycloalkane has the greatest ring strain?
A) Cyclopropane
B) Cyclobutane
C) Cyclopentane
D) Cyclohexane
E) Cycloheptane
A) Cyclopropane
B) Cyclobutane
C) Cyclopentane
D) Cyclohexane
E) Cycloheptane
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58
The graph below is a plot of the relative energies of the various conformations of: 
A) Ethane
B) Propane
C) Chloroethane
D) 1-Chloropropane (C1-C2 rotation)
E) Butane (C1-C2 rotation)

A) Ethane
B) Propane
C) Chloroethane
D) 1-Chloropropane (C1-C2 rotation)
E) Butane (C1-C2 rotation)
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59
The least stable conformation of cyclohexane is the:
A) boat.
B) twist boat.
C) chair.
D) half-chair.
E) twist chair.
A) boat.
B) twist boat.
C) chair.
D) half-chair.
E) twist chair.
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60
The least stable conformation of butane is: 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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61
Which conformation represents the most stable conformation of trans-1-bromo-4-methylcyclohexane? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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62
The most stable conformation of cis-1-tert-butyl-2-methylcyclohexane is the one in which:
A) the tert-butyl group is axial and the methyl group is equatorial.
B) the methyl group is axial and the tert-butyl group is equatorial.
C) both groups are axial.
D) both groups are equatorial.
E) the twist boat conformation is adopted.
A) the tert-butyl group is axial and the methyl group is equatorial.
B) the methyl group is axial and the tert-butyl group is equatorial.
C) both groups are axial.
D) both groups are equatorial.
E) the twist boat conformation is adopted.
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63
The most stable conformation of trans-1-tert-butyl-2-methylcyclohexane is the one in which:
A) the tert-butyl group is axial and the methyl group is equatorial.
B) the methyl group is axial and the tert-butyl group is equatorial.
C) both groups are axial.
D) both groups are equatorial.
E) the molecule is in the half chair conformation.
A) the tert-butyl group is axial and the methyl group is equatorial.
B) the methyl group is axial and the tert-butyl group is equatorial.
C) both groups are axial.
D) both groups are equatorial.
E) the molecule is in the half chair conformation.
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64

trans-1,2-Dibromocyclohexane is represented by structure(s):
A) I
B) II
C) III
D) II and III
E) I and II
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65
How many moles of hydrogen (H2)will react with 3-cyclobutylpropan-1-ol?
A) 1
2
B) 2
C) 3
D) 4
E) None of the above
A) 1
2
B) 2
C) 3
D) 4
E) None of the above
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66
What structure represents the most stable conformation of cis-1,3-dimethylcyclohexane? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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67
Select the structure for cis-3-methyl-6-vinylcyclohexene. 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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68
Catalytic hydrogenation of which of the following will yield 2-methylpentane?
A) 2-methyl-1-pentene
2
B) 2-methyl-2-pentene
C) 4-methyl-2-pentene
D) 4-methyl-1-pentene
E) All of the above
A) 2-methyl-1-pentene
2
B) 2-methyl-2-pentene
C) 4-methyl-2-pentene
D) 4-methyl-1-pentene
E) All of the above
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69
In the most stable conformation of cis-1,4-dimethylcyclohexane,the methyl groups are:
A) one axial,one equatorial.
B) both axial.
C) both equatorial.
D) alternating between being both axial and both equatorial.
E) None of the above
A) one axial,one equatorial.
B) both axial.
C) both equatorial.
D) alternating between being both axial and both equatorial.
E) None of the above
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70
Which of these C10H18 isomers is predicted to be the most stable? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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71
Which of the following will have the same energy after undergoing ring flip? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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72
The twist boat conformation is the preferred conformation for this compound.
A) cis-1,4-Di-tert-butylcyclohexane
B) trans-1,4-Di-tert-butylcyclohexane
C) cis-1,3-Di-tert-butylcyclohexane
D) trans-1,2-Di-tert-butylcyclohexane
E) None of these
A) cis-1,4-Di-tert-butylcyclohexane
B) trans-1,4-Di-tert-butylcyclohexane
C) cis-1,3-Di-tert-butylcyclohexane
D) trans-1,2-Di-tert-butylcyclohexane
E) None of these
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73
How many moles of hydrogen (H2)will react with (trans,trans)-hepta-3,5-dien-1-yne?
A) 1
2
B) 2
C) 3
D) 4
E) 5
A) 1
2
B) 2
C) 3
D) 4
E) 5
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74
The most stable conformation of trans-1-tert-butyl-3-methylcyclohexane is the one in which:
A) the tert-butyl group is axial and the methyl group is equatorial.
B) the methyl group is axial and the tert-butyl group is equatorial.
C) both groups are axial.
D) both groups are equatorial.
E) the twist boat conformation is adopted.
A) the tert-butyl group is axial and the methyl group is equatorial.
B) the methyl group is axial and the tert-butyl group is equatorial.
C) both groups are axial.
D) both groups are equatorial.
E) the twist boat conformation is adopted.
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75
cis-1,3-Dibromocyclohexane is represented by structure(s): 
A) I
B) II
C) III
D) II and III
E) I and II

A) I
B) II
C) III
D) II and III
E) I and II
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76
Which of the following can be described as trans isomers?
A) I
B) II,V
C) III,IV
D) I,III and IV
E) None of the above are trans isomers.

A) I
B) II,V
C) III,IV
D) I,III and IV
E) None of the above are trans isomers.
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77

cis-1,2-Dibromocyclohexane is represented by structure(s):
A) I
B) II
C) III
D) II and III
E) I and II
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78
Select the reagents necessary to convert cyclopentene into cyclopentane.
A) H2 and Ni
B) H2O
C) Heat
D) Zn,H3O+
E) Light
A) H2 and Ni
B) H2O
C) Heat
D) Zn,H3O+
E) Light
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79
Which alkene would yield 3-methylpentane when subjected to catalytic hydrogenation?
A)

B)

C)

D)

E)

A)

B)

C)

D)

E)

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80
Which of the following can be described as cis isomers? 
A) I
B) II,V
C) III,IV
D) I,III and IV
E) None of the above are cis isomers.

A) I
B) II,V
C) III,IV
D) I,III and IV
E) None of the above are cis isomers.
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