One commercial synthesis of ketoprofen (the active ingredient in Actron and a score of other over-the-counter and prescription nonsteroidal anti-inflammatory drug preparations) gives the enantiomer shown in 93% enantiomeric excess. H CH Он (a) Assign an R or S configuration to this enantiomer of ketoprofen. R (b) What are the percentages of R and S enantiomers in the mixture? (Enter unrounded values.) R: S: 96 96

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
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One commercial synthesis of ketoprofen (the active ingredient in Actron and a score of other over-the-counter and prescription nonsteroidal anti-inflammatory drug preparations) gives the enantiomer
shown in 93% enantiomeric excess.
H
CH3
он
(a) Assign an R or S configuration to this enantiomer of ketoprofen.
R
S
What are the percentages of R and S enantiomers in the mixture? (Enter unrounded values.)
(b)
R:
%
S:
%
Transcribed Image Text:One commercial synthesis of ketoprofen (the active ingredient in Actron and a score of other over-the-counter and prescription nonsteroidal anti-inflammatory drug preparations) gives the enantiomer shown in 93% enantiomeric excess. H CH3 он (a) Assign an R or S configuration to this enantiomer of ketoprofen. R S What are the percentages of R and S enantiomers in the mixture? (Enter unrounded values.) (b) R: % S: %
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