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castortr0y [4]
3 years ago
7

(+)-Carvone and (-)-carvone differ in the orientations of the substituents around which of the following carbon atoms?

Chemistry
1 answer:
myrzilka [38]3 years ago
5 0

Answer:

The correct option is: B. Carbon 5 only

Explanation:

Carvone is a naturally-occurring monoterpenoid consisting of a six-membered cyclic ring. <u>The </u><u><em>carbon-5</em></u><u> of this cyclic ring of Carvone is </u><u><em>chiral, </em></u><u>due to which Carvone exhibits </u><u><em>enantiomerism</em></u><u>.</u>

The two <em>enantiomeric forms</em> of Carvone are: R-(–)-carvone, or L-carvone, and S-(+)-carvone, or D-carvone.

<em><u>These two enantiomeric forms differ in the orientation of the substituents on the chiral carbon-5.</u></em>

<u />

<u>Therefore, the correct option is B. Carbon 5 only.</u>

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