Please explain properly. Q16. Ibuprofen, an example of an NSAID, is the active ingredient in several popular over-the-counter analgesics in the U.S., and it is sold in racemic form, even though only the S-enantiomer is pharmacologically active. Suggest methods that might be used to obtain or prepare ibuprofen in enantiomerically pure form, based on processes and reactions you learned. H CH3 (CH3)2CHCH₂ S-ibuprofen CO₂H

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
Chapter23: Amines
Section: Chapter Questions
Problem 23.19P
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Please explain properly.
Q16. Ibuprofen, an example of an NSAID, is the active ingredient in several popular over-the-counter
analgesics in the U.S., and it is sold in racemic form, even though only the S-enantiomer is
pharmacologically active. Suggest methods that might be used to obtain or prepare ibuprofen in
enantiomerically pure form, based on processes and reactions you learned.
H CH3
(CH3)2CHCH₂
S-ibuprofen
CO₂H
Transcribed Image Text:Please explain properly. Q16. Ibuprofen, an example of an NSAID, is the active ingredient in several popular over-the-counter analgesics in the U.S., and it is sold in racemic form, even though only the S-enantiomer is pharmacologically active. Suggest methods that might be used to obtain or prepare ibuprofen in enantiomerically pure form, based on processes and reactions you learned. H CH3 (CH3)2CHCH₂ S-ibuprofen CO₂H
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