(a) Which of the following drugs is more hydrolytically labile? Briefly explain. OH H OH مممممم CO₂H Clavulanic acid Loperamide (b) For each of the above drugs, indicate ONE functional group that is prone to oxidation. (c) One of the degradation products of clavulanic acid in an acidic environment is the following: HO₂C OH HN CO₂H Draw the mechanism of this degradation reaction.

Chemistry for Today: General, Organic, and Biochemistry
9th Edition
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Chapter16: Amines And Amides
Section: Chapter Questions
Problem 16.68E
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(a) Which of the following drugs is more hydrolytically labile? Briefly explain.
OH
H
OH
مممممم
CO₂H
Clavulanic acid
Loperamide
(b) For each of the above drugs, indicate ONE functional group that is prone to oxidation.
(c) One of the degradation products of clavulanic acid in an acidic environment is the following:
HO₂C
OH
HN
CO₂H
Draw the mechanism of this degradation reaction.
Transcribed Image Text:(a) Which of the following drugs is more hydrolytically labile? Briefly explain. OH H OH مممممم CO₂H Clavulanic acid Loperamide (b) For each of the above drugs, indicate ONE functional group that is prone to oxidation. (c) One of the degradation products of clavulanic acid in an acidic environment is the following: HO₂C OH HN CO₂H Draw the mechanism of this degradation reaction.
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