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Can the two compounds be separated by distillation? Why or why not? (1S,2S,3R,5S)-Pinanediol and (1S,2R,3R,5R)-Pinanediol

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Yes. These compounds...

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Provide a Fischer projection of (2R,3R,4S)-2,3,4-trichloroheptane.

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Draw the structure of (S)-3-chloro-3-methylhexane. Take particular care to indicate stereochemistry properly.

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What term describes the structural relationship between (2R,3R,4S) -2,3,4-trichloroheptane and (2R,3R,4R) -2,3,4-trichloroheptane?


A) not isomers
B) constitutional isomers
C) enantiomers
D) diastereomers
E) conformers

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Which of the following terms best describes the pair of compounds shown: enantiomers, diastereomers, or the same compound? Which of the following terms best describes the pair of compounds shown: enantiomers, diastereomers, or the same compound?

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Is the molecule shown below chiral or achiral? Is the molecule shown below chiral or achiral?

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chiral

Label each asymmetric carbon in the compound below as R or S. Label each asymmetric carbon in the compound below as R or S.

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11eab5e1_c8bd_ea81_9bae_c5fd1e08f291_TB6199_00

If possible, draw the structure of the enantiomer of the molecule shown below. If possible, draw the structure of the enantiomer of the molecule shown below.

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The compound is an a...

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Can one separate a mixture of enantiomers by gas chromatography? Explain.

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Provided the compounds can be volatilize...

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How many asymmetric carbons are present in the compound below? How many asymmetric carbons are present in the compound below?

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Assign the proper configurational label, R or S, to the chiral carbon in the molecule shown below. Assign the proper configurational label, R or S, to the chiral carbon in the molecule shown below.

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The stereochemical configuration of D-Threonine is (2R, 3S) . Which of the following structures corresponds to the correct configuration? The stereochemical configuration of D-Threonine is (2R, 3S) . Which of the following structures corresponds to the correct configuration?   A)  I B)  II C)  III D)  IV


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

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Which of the following terms best describes the pair of compounds shown: enantiomers, diastereomers, or the same compound? Which of the following terms best describes the pair of compounds shown: enantiomers, diastereomers, or the same compound?

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the same compound

Which of the statements below correctly describes an achiral molecule?


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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________ are isomers which have the same bonding sequence but differ in the orientation of their atoms in space.

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Is the mirror image of the following molecule an enantiomer or is it superimposable with it? Is the mirror image of the following molecule an enantiomer or is it superimposable with it?

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Superimpos...

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Which of the following statements is (are) true for the compound cis-1,2-dichlorocyclopropane?


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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Predict the specific rotation of the compound shown. Predict the specific rotation of the compound shown.   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.


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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Is it theoretically possible to separate the pair of compounds below by distillation? Explain briefly. Is it theoretically possible to separate the pair of compounds below by distillation? Explain briefly.

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Yes. The molecules a...

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Which of the following statements is (are) true for the compound (3R, 4R) -3,4-dimethylhexane?


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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