Deck 5: Stereochemistry: Chiral Molecules
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Deck 5: Stereochemistry: Chiral Molecules
1
Which of the following is the enantiomer of the following substance? 
A) I
B) II
C) III
D) It does not have a non-superposable enantiomer.
E) Both II and III

A) I
B) II
C) III
D) It does not have a non-superposable enantiomer.
E) Both II and III
It does not have a non-superposable enantiomer.
2
What is the molecular formula for the alkane of smallest molecular weight which possesses a stereogenic center?
A) C4H10
B) C5H12
C) C6H14
D) C7H16
E) C8H18
A) C4H10
B) C5H12
C) C6H14
D) C7H16
E) C8H18
C7H16
3
Which compound would show optical activity?
A) cis-1,4- Dimethylcyclohexane
B) trans-1,4- Dimethylcyclohexane
C) cis-1,4- Dimethylcycloheptane
D) trans-1,4- Dimethylcycloheptane
E) More than one of these
A) cis-1,4- Dimethylcyclohexane
B) trans-1,4- Dimethylcyclohexane
C) cis-1,4- Dimethylcycloheptane
D) trans-1,4- Dimethylcycloheptane
E) More than one of these
trans-1,4- Dimethylcycloheptane
4
Which molecule is achiral? 
A) I
B) II
C) III
D) More than one of the above
E) None of the above

A) I
B) II
C) III
D) More than one of the above
E) None of the above
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5
Which structure represents (S)-2-bromobutane? 
A) I
B) II
C) III
D) More than one of the above
E) None of the above

A) I
B) II
C) III
D) More than one of the above
E) None of the above
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6
How many stereogenic centers are there in Lovastatin ( Mevacor® : a cholesterol-lowering drug)? 
A) 4
B) 5
C) 6
D) 7
E) 8

A) 4
B) 5
C) 6
D) 7
E) 8
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7
Which of the following represent (R)-2-butanol? 
A) III and V
B) I,III,IV and V
C) I,IV and V
D) I and III
E) I,II,IV and V

A) III and V
B) I,III,IV and V
C) I,IV and V
D) I and III
E) I,II,IV and V
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8
Enantiomers are:
A) molecules that have a mirror image.
B) molecules that have at least one stereogenic center.
C) non-superposable molecules.
D) non-superposable constitutional isomers.
E) non-superposable molecules that are mirror images of each other.
A) molecules that have a mirror image.
B) molecules that have at least one stereogenic center.
C) non-superposable molecules.
D) non-superposable constitutional isomers.
E) non-superposable molecules that are mirror images of each other.
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9
Which structure represents (R)-1-chloro-1-fluoroethane? 
A) I
B) II
C) III
D) More than one of the above
E) None of the above

A) I
B) II
C) III
D) More than one of the above
E) None of the above
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10
Which structure represents (S)-1-chloro-1-fluoroethane? 
A) I
B) II
C) III
D) More than one of the above
E) None of the above

A) I
B) II
C) III
D) More than one of the above
E) None of the above
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11
Pairs of enantiomers are: 
A) I,II and III,IV
B) I,II
C) III,IV
D) IV,V
E) None of the structures

A) I,II and III,IV
B) I,II
C) III,IV
D) IV,V
E) None of the structures
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12
What is the total number of compounds,stereoisomers included,designated by the general name "dichlorocyclopentane"?
A) 4
B) 5
C) 7
D) 8
E) 9
A) 4
B) 5
C) 7
D) 8
E) 9
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13
Chiral molecules are represented by: 
A) I,II,III,IV and V
B) I,II,III and IV
C) I and II
D) III and IV
E) IV alone

A) I,II,III,IV and V
B) I,II,III and IV
C) I and II
D) III and IV
E) IV alone
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14
Which of the following is NOT true of enantiomers? They have the same:
A) boiling point.
B) melting point.
C) specific rotation.
D) density.
E) chemical reactivity toward achiral reagents.
A) boiling point.
B) melting point.
C) specific rotation.
D) density.
E) chemical reactivity toward achiral reagents.
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15
Which of these is a comparatively insignificant factor affecting the magnitude of specific optical rotation?
A) Concentration of the substance of interest
B) Purity of the sample
C) Temperature of the measurement
D) Length of the sample tube
E) All of the above are equally significant.
A) Concentration of the substance of interest
B) Purity of the sample
C) Temperature of the measurement
D) Length of the sample tube
E) All of the above are equally significant.
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16
Cis-trans isomers are:
A) diastereomers.
B) enantiomers.
C) stereoisomers.
D) constitutional isomers.
E) More than one of these
A) diastereomers.
B) enantiomers.
C) stereoisomers.
D) constitutional isomers.
E) More than one of these
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17
(R)-2-Chlorobutane is represented by: 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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18
Which of the following is true about any (R)-enantiomer?
A) It is dextrorotatory.
B) It is levorotatory.
C) It is an equal mixture of + and -.
D) It is the mirror image of the (S)-enantiomer.
E) (R)indicates a racemic mixture.
A) It is dextrorotatory.
B) It is levorotatory.
C) It is an equal mixture of + and -.
D) It is the mirror image of the (S)-enantiomer.
E) (R)indicates a racemic mixture.
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19
Which of the following is true of any (S)-enantiomer?
A) It rotates plane-polarized light to the right.
B) It rotates plane-polarized light to the left.
C) It is a racemic form.
D) It is the mirror image of the corresponding (R)-enantiomer.
E) It has the highest priority group on the left.
A) It rotates plane-polarized light to the right.
B) It rotates plane-polarized light to the left.
C) It is a racemic form.
D) It is the mirror image of the corresponding (R)-enantiomer.
E) It has the highest priority group on the left.
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20
Which molecule is achiral? 
A) I
B) II
C) III
D) More than one of these
E) None of these

A) I
B) II
C) III
D) More than one of these
E) None of these
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21
Of the compounds which correspond to the general name "dichlorocyclobutane",how many are optically active?
A) 0
B) 1
C) 2
D) 3
E) 4
A) 0
B) 1
C) 2
D) 3
E) 4
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22
Which of the following is(are)meso compound(s)? 
A) I
B) II
C) III
D) Both II and III
E) Both I and III

A) I
B) II
C) III
D) Both II and III
E) Both I and III
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23
Which statement is not true for a meso compound?
A) The specific rotation is 0º.
B) There are one or more planes of symmetry.
C) A single molecule is identical to its mirror image.
D) More than one stereogenic center must be present.
E) The stereochemical labels, (R)and (S),must be identical for each stereogenic center.
A) The specific rotation is 0º.
B) There are one or more planes of symmetry.
C) A single molecule is identical to its mirror image.
D) More than one stereogenic center must be present.
E) The stereochemical labels, (R)and (S),must be identical for each stereogenic center.
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24
What is the percent composition of a mixture of (S)-(+)-2-butanol,[ ]
= +13.52º,and (R)-(-)-2-butanol,[ ]
= -13.52º,with a specific rotation [ ]
= +6.76º?
A) 75%(R)25%(S)
B) 25%(R)75%(S)
C) 50%(R)50%(S)
D) 67%(R)33%(S)
E) 33%(R)67%(S)
![<strong>What is the percent composition of a mixture of (S)-(+)-2-butanol,[ \alpha ]<sub> </sub> <sub> </sub> <sub> </sub> <sup> </sup> = +13.52º,and (R)-(-)-2-butanol,[ \alpha ]<sub> </sub> <sub> </sub> <sub> </sub> <sup> </sup>= -13.52º,with a specific rotation [ \alpha ] <sub> </sub> <sup> </sup> = +6.76º?</strong> A) 75%(R)25%(S) B) 25%(R)75%(S) C) 50%(R)50%(S) D) 67%(R)33%(S) E) 33%(R)67%(S)](https://storage.examlex.com/TB5901/11ea9a02_1aa7_114f_8bb6_83b8072aaa40_TB5901_11.jpg)
= +13.52º,and (R)-(-)-2-butanol,[ ]
![<strong>What is the percent composition of a mixture of (S)-(+)-2-butanol,[ \alpha ]<sub> </sub> <sub> </sub> <sub> </sub> <sup> </sup> = +13.52º,and (R)-(-)-2-butanol,[ \alpha ]<sub> </sub> <sub> </sub> <sub> </sub> <sup> </sup>= -13.52º,with a specific rotation [ \alpha ] <sub> </sub> <sup> </sup> = +6.76º?</strong> A) 75%(R)25%(S) B) 25%(R)75%(S) C) 50%(R)50%(S) D) 67%(R)33%(S) E) 33%(R)67%(S)](https://storage.examlex.com/TB5901/11ea9a02_1aa7_1150_8bb6_eff12c99cb03_TB5901_11.jpg)
= -13.52º,with a specific rotation [ ]
![<strong>What is the percent composition of a mixture of (S)-(+)-2-butanol,[ \alpha ]<sub> </sub> <sub> </sub> <sub> </sub> <sup> </sup> = +13.52º,and (R)-(-)-2-butanol,[ \alpha ]<sub> </sub> <sub> </sub> <sub> </sub> <sup> </sup>= -13.52º,with a specific rotation [ \alpha ] <sub> </sub> <sup> </sup> = +6.76º?</strong> A) 75%(R)25%(S) B) 25%(R)75%(S) C) 50%(R)50%(S) D) 67%(R)33%(S) E) 33%(R)67%(S)](https://storage.examlex.com/TB5901/11ea9a02_1aa7_1151_8bb6_abeed926dead_TB5901_11.jpg)
= +6.76º?
A) 75%(R)25%(S)
B) 25%(R)75%(S)
C) 50%(R)50%(S)
D) 67%(R)33%(S)
E) 33%(R)67%(S)
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25
The reaction of
with H2/Ni forms:
A) 2-methylheptane
B) (R)-2-methyl-5-heptanol
C) (S)-6-methyl-3-heptanol
D) (R and S)-6-methyl-3-heptanol
E) Achiral 6,6-dimethyl-3-hexanol

A) 2-methylheptane
B) (R)-2-methyl-5-heptanol
C) (S)-6-methyl-3-heptanol
D) (R and S)-6-methyl-3-heptanol
E) Achiral 6,6-dimethyl-3-hexanol
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26
Which of the following is a meso compound? 
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 can be said with certainty if a compound has [ ]
= -9.25 ?
A) The compound has the (S)configuration.
B) The compound has the (R)configuration.
C) The compound is not a meso form.
D) The compound possesses only one stereogenic center.
E) The compound has an optical purity of less than 100%.
![<strong>What can be said with certainty if a compound has [ \alpha ] <sub> </sub> = -9.25 ?</strong> A) The compound has the (S)configuration. B) The compound has the (R)configuration. C) The compound is not a meso form. D) The compound possesses only one stereogenic center. E) The compound has an optical purity of less than 100%.](https://storage.examlex.com/TB5901/11ea9a02_1aa6_c32e_8bb6_b3955c9935a2_TB5901_11.jpg)
A) The compound has the (S)configuration.
B) The compound has the (R)configuration.
C) The compound is not a meso form.
D) The compound possesses only one stereogenic center.
E) The compound has an optical purity of less than 100%.
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28
How many chiral stereoisomers can be drawn for CH3CHFCHFCH(CH3)2?
A) 1
B) 2
C) 3
D) 4
E) 8
A) 1
B) 2
C) 3
D) 4
E) 8
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29
Which of the following is(are)meso? 
A) I
B) II
C) III
D) IV
E) Two of the above

A) I
B) II
C) III
D) IV
E) Two of the above
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30
How many discrete dimethylcyclopropanes are there?
A) 2
B) 3
C) 4
D) 5
E) 6
A) 2
B) 3
C) 4
D) 5
E) 6
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31
The structures
represent:
A) a single compound.
B) enantiomers.
C) meso forms.
D) diastereomers.
E) conformational isomers.

A) a single compound.
B) enantiomers.
C) meso forms.
D) diastereomers.
E) conformational isomers.
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32
The compounds whose molecules are shown below would have: 
A) the same melting point.
B) different melting points.
C) equal but opposite optical rotations.
D) More than one of the above
E) None of the above

A) the same melting point.
B) different melting points.
C) equal but opposite optical rotations.
D) More than one of the above
E) None of the above
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33
CH3CHBrCH2CHClCH3 is the generalized representation of what number of stereoisomers?
A) 3
B) 4
C) 5
D) 6
E) 7
A) 3
B) 4
C) 5
D) 6
E) 7
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34
Which molecule is a meso compound? 
A) I
B) II
C) III
D) More than one of the above
E) None of the above

A) I
B) II
C) III
D) More than one of the above
E) None of the above
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35
I and II are: 
A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.

A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.
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36
For the generalized structure BrCH2CHClCH2CHClCH2Br there exists what number of stereoisomers?
A) 2
B) 3
C) 4
D) 6
E) 8
A) 2
B) 3
C) 4
D) 6
E) 8
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37
An alkane which can exhibit optical activity is:
A) Neopentane
B) Isopentane
C) 3-Methylpentane
D) 3-Methylhexane
E) 2,3-Dimethylbutane
A) Neopentane
B) Isopentane
C) 3-Methylpentane
D) 3-Methylhexane
E) 2,3-Dimethylbutane
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38
I and II are: 
A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.

A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.
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39
In the absence of specific data,it can only be said that (R)-2-bromopentane is:
A) dextrorotatory (+).
B) levorotatory (-).
C) optically inactive.
D) achiral.
E) analogous in absolute configuration to (R)-2-chloropentane.
A) dextrorotatory (+).
B) levorotatory (-).
C) optically inactive.
D) achiral.
E) analogous in absolute configuration to (R)-2-chloropentane.
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40
If a solution of a compound (30.0 g/100 mL of solution)has a measured rotation of +15º in a 2 dm tube,the specific rotation is:
A) +50
B) +25
C) +15
D) +7.5
E) +4.0
A) +50
B) +25
C) +15
D) +7.5
E) +4.0
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41
The molecules below are: 
A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) stereoisomers.

A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) stereoisomers.
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42
The molecules below are: 
A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these

A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these
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43
The molecules below are: 
A) structural isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these

A) structural isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these
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44
The molecules below are: 
A) enantiomers.
B) diastereomers.
C) constitutional isomers.
D) two different conformations of the same molecule.
E) not isomeric.

A) enantiomers.
B) diastereomers.
C) constitutional isomers.
D) two different conformations of the same molecule.
E) not isomeric.
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45
I and II are: 
A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.

A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.
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46
Which statement is true of 1,3-dimethylcyclobutane?
A) Only one form of the compound is possible.
B) Two diastereomeric forms are possible.
C) Two sets of enantiomers are possible.
D) Two enantiomeric forms and one meso compound are possible.
E) None of the previous statements is true.
A) Only one form of the compound is possible.
B) Two diastereomeric forms are possible.
C) Two sets of enantiomers are possible.
D) Two enantiomeric forms and one meso compound are possible.
E) None of the previous statements is true.
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47
I and II are: 
A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.

A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.
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48
I and II are: 
A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.

A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.
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49
The molecules below are: 
A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these

A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these
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50
The molecules shown are: 
A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these

A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these
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51
I and II are: 
A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.

A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.
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52
The molecules below are: 
A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these

A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these
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53
The molecules below are: 
A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these

A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these
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54
I and II are: 
A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.

A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.
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55
The two compounds shown below are:
are:
A) identical.
B) enantiomers.
C) diastereomers.
D) conformational isomers.
E) meso forms.

A) identical.
B) enantiomers.
C) diastereomers.
D) conformational isomers.
E) meso forms.
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56
I and II are: 
A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.

A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.
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57
Hexane and 3-methylpentane are examples of:
A) enantiomers.
B) stereoisomers.
C) diastereomers.
D) constitutional isomers.
E) None of these
A) enantiomers.
B) stereoisomers.
C) diastereomers.
D) constitutional isomers.
E) None of these
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58
The molecules below are: 
A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these

A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these
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59
The molecules below are: 
A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these

A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these
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60
The molecules below are: 
A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these

A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these
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61
Which is a meso compound?
A) (2R,3R)-2,3-Dibromobutane
B) (2R,3S)-2,3-Dibromopentane
C) (2R,4R)-2,4-Dibromopentane
D) (2R,4S)-2,4-Dibromopentane
E) (2R,4S)-2,4-Dibromohexane
A) (2R,3R)-2,3-Dibromobutane
B) (2R,3S)-2,3-Dibromopentane
C) (2R,4R)-2,4-Dibromopentane
D) (2R,4S)-2,4-Dibromopentane
E) (2R,4S)-2,4-Dibromohexane
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62
The compounds whose molecules are shown below would have: 
A) the same melting point.
B) different melting points.
C) equal but opposite optical rotations.
D) More than one of the above
E) None of the above

A) the same melting point.
B) different melting points.
C) equal but opposite optical rotations.
D) More than one of the above
E) None of the above
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63

Which of the compounds above (I-IV)represent enantiomers?
A) I and II
B) II and III
C) III and IV
D) II and IV
E) "III and IV"
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64
The molecules shown are: 
A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these

A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these
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65
I and II are: 
A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.

A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.
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66
Which compound does NOT possess a plane of symmetry? 
A) I,II and V
B) I,III and IV
C) II,III and IV
D) III and IV
E) V

A) I,II and V
B) I,III and IV
C) II,III and IV
D) III and IV
E) V
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67
I and II are: 
A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.

A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.
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68
I and II are: 
A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.

A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.
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69
Which molecule has a plane of symmetry? 
A) I
B) II
C) III
D) More than one of these
E) None of these

A) I
B) II
C) III
D) More than one of these
E) None of these
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70

Which compound above (I-IV)is (2R,3R)-2,3-butanediol?
A) I
B) II
C) III
D) IV
E) None of these
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71
Which of the following substances is achiral ? 
A) I
B) II
C) III
D) IV
E) More than one of these

A) I
B) II
C) III
D) IV
E) More than one of these
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72
The The molecules shown are: 
A) enantiomers.
B) diastereomers.
C) constitutional isomers.
D) two conformations of the same molecule.
E) not isomeric.

A) enantiomers.
B) diastereomers.
C) constitutional isomers.
D) two conformations of the same molecule.
E) not isomeric.
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73
Which molecule has a plane of symmetry? 
A) I
B) II
C) III
D) More than one of these
E) None of these

A) I
B) II
C) III
D) More than one of these
E) None of these
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74
I and II are: 
A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.

A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.
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75
I and II are: 
A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.

A) constitutional isomers.
B) enantiomers.
C) identical.
D) diastereomers.
E) not isomeric.
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76

Which compound above (I-IV)is a meso compound?
A) I
B) II
C) III
D) IV
E) None of these
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77
Which of the following molecules is achiral?
A) (2R,3R)-2,3-Dichloropentane
B) (2R,3S)-2,3-Dichloropentane
C) (2S,4S)-2,4-Dichloropentane
D) (2S,4R)-2,4-Dichloropentane
E) Two of these
A) (2R,3R)-2,3-Dichloropentane
B) (2R,3S)-2,3-Dichloropentane
C) (2S,4S)-2,4-Dichloropentane
D) (2S,4R)-2,4-Dichloropentane
E) Two of these
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78

Which compounds above (I-IV)form a set of stereoisomers?
A) I,II and III
B) II,III and IV
C) II and III
D) I,III and IV
E) I,II,III and IV
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79
Which molecule is a meso compound? 
A) I and II
B) IV and V
C) II and III
D) I,II and III
E) None of the above

A) I and II
B) IV and V
C) II and III
D) I,II and III
E) None of the above
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80
The molecules shown are: 
A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these

A) constitutional isomers.
B) enantiomers.
C) diastereomers.
D) identical.
E) None of these
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