Questions
Questions

CHE 008B A01 SS1 2025 Lecture 14 - Claisen Condensation

Multiple choice

Which of these could be a nucleophile for a Claisen Condensation? (select all that apply)

Options
A.aldehyde with alpha H
B.aldehyde with no alpha H
C.ketone with no alpha H
D.ketone with 2+ alpha H
E.ester with 2+ alpha H
F.ester with 1 alpha H
G.ester with no alpha H
H.carboxylic acid with alpha H
I.carboxylic acid with no alpha H
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Step-by-Step Analysis
To determine which species could act as a nucleophile in a Claisen Condensation, recall that the nucleophile is typically an enolate formed from a carbonyl compound that has an alpha proton, which can be deprotonated to give a resonance-stabilized anion. Option A: aldehyde with alpha H Reasoning: Aldehydes can form enolates if there are alpha hydrogens, but in classical Claisen condensations the nucleophile is an enolate derived from an ester (not an aldehyde). Aldehydes are more commonly electrophiles in related reactions (e.g., aldol condensations) rather than ser......Login to view full explanation

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