O On a reaction with acid, 4-pyrone is protonated on the carbonyl-group oxygen to give a stable cationic product. Using resonance structures and the Huckel 4n+2 rule, explain why the protonated product is so stable. 4-Pyrone

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter19: Aldehydes And Ketones: Nucleophilic Addition Reactions
Section19.SE: Something Extra
Problem 28VC
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OOn a reaction with acid, 4-pyrone is protonated on the
carbonyl-group oxygen to give a stable cationic
product. Using resonance structures and the Huckel
4n+2 rule, explain why the protonated product is so
stable.
4-Pyrone
Transcribed Image Text:OOn a reaction with acid, 4-pyrone is protonated on the carbonyl-group oxygen to give a stable cationic product. Using resonance structures and the Huckel 4n+2 rule, explain why the protonated product is so stable. 4-Pyrone
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