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Multiple Choice
A) not isomers
B) constitutional isomers
C) enantiomers
D) diastereomers
E) conformers
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Multiple Choice
A) I
B) II
C) III
D) IV
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Multiple Choice
A) The molecule has a nonsuperimposable mirror image.
B) The molecule exhibits optical activity when it interacts with plane-polarized light.
C) The molecule has an enantiomer.
D) The molecule might be a meso form.
E) None of the above
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Multiple Choice
A) This compound is chiral.
B) The enantiomer of this compound is trans-1,2-dichlorocyclopropane.
C) This compound contains no asymmetric carbons.
D) all of the above
E) none of the above
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Multiple Choice
A) It is impossible to predict; it must be determined experimentally.
B) Because both asymmetric centers are R, the compound is dextrorotatory.
C) Because both asymmetric centers are S, the compound is levorotatory.
D) Zero; the compound is achiral.
E) Because this compound represents a racemic mixture, the compound is dextrorotatory.
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Multiple Choice
A) This compound is chiral.
B) The enantiomer of this compound is (3S, 4S) -3,4-dimethylhexane.
C) This compound is a diastereomer of (3R, 4S) -3,4-dimethylhexane.
D) all of the above
E) none of the above
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