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Which molecule has a plane of symmetry? 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

F) All of the above
G) C) and D)

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D

Draw a dash-wedge structure for (1S,2S,5R)-5-methyl-2-propylcyclohexanol

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The molecules shown are: 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

F) All of the above
G) B) and E)

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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

F) C) and E)
G) A) and B)

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Draw a dash-wedge structure for (1R,2S,3S)-3-bromo-2-vinylcyclohexanol

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Which structure represents (S) -2-bromobutane? 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

F) A) and B)
G) A) and C)

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For the generalized structure BrCH2CHClCH2CHClCH2Br there exists what number of stereoisomers?


A) 2
B) 3
C) 4
D) 6
E) 8

F) C) and E)
G) B) and D)

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Draw a dash-wedge structure for (3R,6R)-3-bromo-6-methylcyclohex-1-ene

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Which molecule is a meso compound? 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

F) All of the above
G) A) and B)

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Draw a dash-wedge structure for (2S,3R)-3-bromo-6,6-dimethyl-7-en-2-ol

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A meso compound has __________ chiral center(s),and is __________ upon its mirror image.

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two or mor...

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A chiral molecule is defined as one that is _____________________ on its mirror image.

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The compounds whose molecules are shown below would have: 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 these E)  None of these


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

F) C) and D)
G) None of the above

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Which structure(s) represent(s) diastereomer(s) of I? Which structure(s) represent(s) diastereomer(s) of I?   A)  II B)  II and III C)  II and IV D)  III and V E)  IV and V


A) II
B) II and III
C) II and IV
D) III and V
E) IV and V

F) A) and E)
G) A) and D)

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  -Which compound above (I-IV) is (2R,3R) -2,3-butanediol? A)  I B)  II C)  III D)  IV E)  None of these -Which compound above (I-IV) is (2R,3R) -2,3-butanediol?


A) I
B) II
C) III
D) IV
E) None of these

F) B) and D)
G) B) and E)

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Chiral molecules are represented by: 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

F) A) and B)
G) A) and C)

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Draw a dash-wedge structure for (1S,3R)-1-ethyl-1,3-dimethylcyclopentane

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11ea9a02_1ab2_d17f_8bb6_ed27a4af67b3_TB5901_00

The molecules below are: 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

F) A) and D)
G) A) and E)

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The molecules below are: 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

F) A) and B)
G) A) and C)

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C

The molecules below are: 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

F) A) and C)
G) B) and D)

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