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I and II are: 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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For the generalized structure BrCH2CHClCH2CHClCH2Br there exists what number of stereoisomers?


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

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How is it possible to differentiate compounds in a racemic mixture?


A) by distilling of one isomer from the other
B) through the use of IR spectroscopy
C) chemical conversion to a diastereomeric mixture
D) how the mixture rotates in plane polarized light
E) it is impossible to differentiate the two compounds

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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

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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 choices.


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

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Draw a dash-wedge structure for (3S,4R)-4-chloro-3,5-dimethylhex-1-yne

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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 choices. E) None of these choices.


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

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To be superposable,when one object is placed on top of another,___.

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all parts ...

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Which compound (I-IV) is a meso compound? Which compound (I-IV) is a meso compound?   A) I B) II C) III D) IV E) None of these choices.


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

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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 choices.

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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 choices.


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

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If a sample is said to contain a 98.0% enantiomeric excess of the compound (+)-camphor,what would be the observed specific rotation if the pure (+)-camphor was found to have a rotation of 44.1?

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A solution of which of these allenes will rotate plane-polarized light? A solution of which of these allenes will rotate plane-polarized light?   A) I B) II C) III D) IV E) V


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

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The molecules shown are: 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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Draw a dash-wedge structure for (2S,3R)-3-bromo-6,6-dimethyloct-7-en-2-ol

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The molecule The molecule   is properly named: A) (3R,4S,5R) -3,5-Dichloro-4-methylhexane B) (2S,3S,4S) -2,4-Dichloro-3-methylhexane C) (2S,3R,4R) -2,4-Dichloro-3-methylhexane D) (2S,3R,4S) -2,4-Dichloro-3-methylhexane E) (2S,3S,4R) -2,4-Dichloro-3-methylhexane is properly named:


A) (3R,4S,5R) -3,5-Dichloro-4-methylhexane
B) (2S,3S,4S) -2,4-Dichloro-3-methylhexane
C) (2S,3R,4R) -2,4-Dichloro-3-methylhexane
D) (2S,3R,4S) -2,4-Dichloro-3-methylhexane
E) (2S,3S,4R) -2,4-Dichloro-3-methylhexane

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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 choices. E) None of these choices.


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

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


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

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Which of these is not a correct Fischer projection formula of the (S) form of 3-bromo-1,1-dichloro-2-propanol? Which of these is not a correct Fischer projection formula of the (S) form of 3-bromo-1,1-dichloro-2-propanol?   A) I B) II C) III D) IV E) V


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

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