Use electronic factors to explain which oxygen is preferentially protonated in carboxylic acids

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
Chapter19: Enolate Anions And Enamines
Section: Chapter Questions
Problem 19.40P: Enamines normally react with methyl iodide to give two products: one arising from alkylation at...
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4.2
4.3
Discuss this observation in detail.
Use electronic factors to explain which oxygen is preferentially protonated in carboxylic
acids
Propose reaction mechanisms between benzoyl chloride with the following reagents:
4-0 pyridino
Transcribed Image Text:4.2 4.3 Discuss this observation in detail. Use electronic factors to explain which oxygen is preferentially protonated in carboxylic acids Propose reaction mechanisms between benzoyl chloride with the following reagents: 4-0 pyridino
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