(c) Explain, using mechanisms, why the (S)-enantiomer of ibuprofen (E) undergoes racemisation under acidic conditions in the body. (E) (S) CO₂H

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter24: Amines And Heterocycles
Section24.SE: Something Extra
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(c) Explain, using mechanisms, why the (S)-enantiomer of ibuprofen (E) undergoes
racemisation under acidic conditions in the body.
(E)
(S) CO₂H
Transcribed Image Text:(c) Explain, using mechanisms, why the (S)-enantiomer of ibuprofen (E) undergoes racemisation under acidic conditions in the body. (E) (S) CO₂H
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