Study Notes On CLAISEN REACTION (CLAISEN SCHMIDT REACTION) (Chemical Science) - Download PDF!

By Astha Singh|Updated : July 22nd, 2022

Are you an Aspirant of CSIR-NET and looking for some short and reliable notes for Chemical Sciences to strong your base for preparations? We have got you covered!

Candidates preparing for their CSIR NET exam can really make their preparation journey easier with the help of some reliable study notes that cover the topics in the most simple way. We at BYJU'S Exam Prep have come up with the idea of providing short notes On CLAISEN REACTION (CLAISEN SCHMIDT REACTION) which comes under the Organic Chemistry section of the Chemical Science syllabus. 

The short notes on CLAISEN REACTION (CLAISEN SCHMIDT REACTION) are developed by our experienced subject-matter experts to provide you with the most standard and authentic set of study materials to be focused upon. The students need the best resources for their preparation to clear the CSIR NET examination, Here are the most reliable study notes to make the topics easier for you and also help you to save your time for the preparations for the upcoming CSIR-NET 2022 exam.

Short Notes On CLAISEN REACTION (CLAISEN SCHMIDT REACTION)

It is a carbon-carbon bond formation reaction Claisen condensation reaction occurs between an aldehyde or ketone having α-hydrogen with aromatic carbonyl compound without α-hydrogen.

This reaction takes place in absence of solvent Dilute alkali, such as sodium hydroxide, is used as a base.

Claisen Schmidt condensation is an example of crossed Aldol process.

In this reaction, a carbon-carbon bond is formed via enolate addition and loss of water to form an α, β-unsaturated carbonyl compound.

General Reaction-

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Reaction Mechanism-

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Note 1:

It involves the condensation between an aromatic aldehyde (or a ketone) with an aliphatic aldehyde or a ketone in presence of dilute alkali to form α, β-unsaturated compounds. Example-

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Note 2:

If benzaldehyde is used in excess, the benzal acetone formed reacts further with another molecule of benzaldehyde to form dibenzalacetone.

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Note 3: 

Acetophenone condenses with benzaldehyde in presence of dilute alkali to form benzalacetophenone or phenyl styryl ketone.

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