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 explanationLog in for full answers
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Similar Questions
Assign each of these statements as True or False. True Intramolecular Claisen condensations prefer 5 or 6 member rings. False Using a ketone as an enolate in a Claisen condensation gives a beta-diester. True Claisen condensations require 1 or more alpha H to form an enolate ion nucleophile to give a good yield. True The product of a Claisen condensation is more acidic than the starting material.
The Claisen condensation first forms an ion which undergoes a to give the beta-ketoester. This product immediately undergoes an acid base reaction because it's pKa is about which is favored over the ester who's pKa is about .
The Claisen condensation is analogous to the reaction of aldehydes but with esters.
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