What is the enantiomeric excess (% ee) of a sample of carvone which exhibits a specific rotation of 55 given that the specific rotation of (S)-carvone is 61? Does the unknown sample primarily have the R or S absolute configuration? *Pick two answers. S 90 74 It is a racemic mixture. 66 R 85

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter3: Stereoisomerism And Chirality
Section3.7: Optical Activity—how Chirality Is Detected In The Laboratory
Problem 3.10P
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What is the enantiomeric excess (% ee) of a sample of carvone which exhibits a specific rotation of 55 given that the specific rotation of (S)-carvone is 61?
Does the unknown sample primarily have the R or S absolute configuration?
*Pick two answers.
S
90
90
74
It is a racemic mixture.
66
R
85
Transcribed Image Text:What is the enantiomeric excess (% ee) of a sample of carvone which exhibits a specific rotation of 55 given that the specific rotation of (S)-carvone is 61? Does the unknown sample primarily have the R or S absolute configuration? *Pick two answers. S 90 90 74 It is a racemic mixture. 66 R 85
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