3) Consider the molecules of but-2-enal and but-3-enal below. Both molecules can be deprotonated by a strong base such as lithium diisopropylamide (LDA). H But-3-enal But-2-enal Which molecule is more acidic? Why? Use a reaction coordinate diagram(s) to explain your answer. H

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
Chapter4: Acids And Bases
Section: Chapter Questions
Problem 4.12P
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3)
Consider the molecules of but-2-enal and but-3-enal
below. Both molecules can be deprotonated by a strong base such as lithium
diisopropylamide (LDA).
H
2
H
But-3-enal
But-2-enal
Which molecule is more acidic? Why? Use a reaction coordinate diagram(s) to
explain your answer.
Transcribed Image Text:3) Consider the molecules of but-2-enal and but-3-enal below. Both molecules can be deprotonated by a strong base such as lithium diisopropylamide (LDA). H 2 H But-3-enal But-2-enal Which molecule is more acidic? Why? Use a reaction coordinate diagram(s) to explain your answer.
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