Use an analysis of resonance effects and leaving-group basicities to explain why acid-catalyzed hydrolysis of esters is

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Use an analysis of resonance effects and leaving-group basicities to explain why acid-catalyzed hydrolysis of esters is faster than acid-catalyzed hydrolysis of amides.

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Organic Chemistry

ISBN: 978-0981519432

5th edition

Authors: Marc Loudon

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Question Posted: Apr 26, 2016 09:14 AM

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Use an analysis of resonance effects and leaving-group basicities to explain why acid-catalyzed hydrolysis of esters is

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Resonance effects The application of the resonance effect f...View the full answer

Organic Chemistry

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