Please answer all parts 3. To the right are two enantiomeric naturalproducts with vastly different olfactoryproperties. I find this example of enantiomericpairs particularly intriguing, as I love carawayand rye, but loathe spearmint:Answer the questions below, with theunderstanding that an optically pure solution ofthe (-)-enantiomer of carvone rotates light(R)-carvonespearmint(S)-carvonecarawaycounterclockwise 60°.a. What would be the observed optical rotation of a solution comprised of a 3:1 ratioof the (+) to (-) enantiomers of carvoneib. A different solution of both carvone enantiomers exhibits an observed optical,.rotation of -10°. Determine the enantiomeric excess for this solution. *c. Which enantiomer (R or S) is in excess in the solution from (b)? How do youknownd. Using your answer from (b) above, calculate the actual percentages of eachenantiomer in the solution.

3. To the right are two enantiomeric natural products with vastly different olfactory properties. I find this example of enantiomeric pairs particularly intriguing, as I love caraway and rye, but loathe spearmint: Answer the questions below, with the understanding that an optically pure solution of the (-)-enantiomer of carvone rotates light counterclockwise 60°. (R)-carvone spearmint (S)-carvone caraway a. What would be the observed optical rotation of a solution comprised of a 3:1 ratio of the (+) to (-) enantiomers of carvone b. A different solution of both carvone enantiomers exhibits an observed optical, rotation of -10°. Determine the enantiomeric excess for this solution. " c. Which enantiomer (R or S) is in excess in the solution from (b)? How do you knowh d. Using your answer from (b) above, calculate the actual percentages of each enantiomer in the solution.

3. To the right are two enantiomeric natural products with vastly different olfactory properties. I find this example of enantiomeric pairs particularly intriguing, as I love caraway and rye, but loathe spearmint: Answer the questions below, with the understanding that an optically pure solution of the (-)-enantiomer of carvone rotates light counterclockwise 60°. (R)-carvone spearmint (S)-carvone caraway a. What would be the observed optical rotation of a solution comprised of a 3:1 ratio of the (+) to (-) enantiomers of carvone b. A different solution of both carvone enantiomers exhibits an observed optical, rotation of -10°. Determine the enantiomeric excess for this solution. " c. Which enantiomer (R or S) is in excess in the solution from (b)? How do you knowh d. Using your answer from (b) above, calculate the actual percentages of each enantiomer in the solution.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 25VC: The following molecular model of a dimethyl-substituted biphenyl represents the lowest-energy...

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