Of course,The Claisen Condensation is typically the reaction between two esters, in the presence of base, leading to formation of an ester enolate that reacts with an uncharged ester, thereby displacing it's "alcohol part" as the leaving group. The sequence leads to the formation of beta ketoesters.
The intramolecular (cyclic) version of the Claisen Condensation is known as the Dieckmann Condensation, and is illustrated through the article, "Dieckmann Condensation Missing Piece."
The Claisen-Schmidt reaction involves the condensation of two carbonyl compounds, typically an aldehyde and a ketone, to form an α,β-unsaturated carbonyl compound. In contrast, aldol condensation involves the condensation of an aldehyde or ketone with itself to form a β-hydroxy carbonyl compound. The key difference is the presence of two different carbonyl compounds in the Claisen-Schmidt reaction, while aldol condensation involves one carbonyl compound reacting with itself.
Yes, it is.
condensation
Yes, condensation reactions build macromolecules.
carbohydrate polymerase reaction is a condensation polymerization reaction
The Claisen-Schmidt reaction involves the condensation of two carbonyl compounds, typically an aldehyde and a ketone, to form an α,β-unsaturated carbonyl compound. In contrast, aldol condensation involves the condensation of an aldehyde or ketone with itself to form a β-hydroxy carbonyl compound. The key difference is the presence of two different carbonyl compounds in the Claisen-Schmidt reaction, while aldol condensation involves one carbonyl compound reacting with itself.
Aldol condensation is the reaction of two aldehydes in the presence of a basic catalyst. The aldol condensation leads to an aldol product, in which an hydroxyl group is attached to the beta carbon of an aldehyde. Claisen condensation is similar to aldol condensation, but is involves two esters instead of two aldehydes. The product of a Claisen condensation is a beta-keto-ester, a compound characterized by an ester with its alpha carbon being a ketone.
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Not really because aldol condensation of 2 CH3CHO would be a major competing process.
(CH3)2CHCOOCH3 should be present in excess because it does not form a stable product from Claisen condensation with itself and it will be able to preferentially react with enolate ions from the first ester. Side reaction ( Condensation of first ester with itself) :- 2 CH3CH2CO2CH3 - > CH3CH2OCO2CH2CH3 + CH3CO2CH2CH3
condensation reaction
A condensation reaction is a chemical reaction where man-made polymers are made. Condensation reaction is a reaction that links monomers with the release of water.
Among the most famous name reactions in organic chemistry are: Diels-Alder reaction Wittig reaction Michael addition Aldol condesation Strecker amino acid synthesis Claisen condensation Cope rearangement Fischer indole synthesis
All condensation reactions proceed with formation of water (H2O). If you look at the reaction mechanism for Aldol condensation, you will observe that water is formed as an end-product of the reaction.
Rainer Ludwig Claisen died on 1930-01-05.