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."
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.
carbohydrate polymerase reaction is a condensation polymerization reaction
No, a neutralization reaction is not the same as a condensation reaction. A neutralization reaction typically involves an acid reacting with a base to produce water and a salt, while a condensation reaction involves the joining of two molecules with the elimination of a small molecule, often water. These reactions serve different purposes and occur under different conditions in chemistry.
The products of a condensation reaction between glucose and fructose are sucrose and water. In this reaction, a glycosidic bond forms between the glucose and fructose molecules, resulting in the formation of the disaccharide sucrose. Water is also produced as a byproduct of the condensation reaction.
Two of the most important from an academic standpoint are the Aldol addition which involves combining aldehyde, ketones or N,N-disubstituted esters to form more complex molecues. In the case of a biological system single collagen proteins are linked to form cross- linked collagen via an aldol addition of 2 aldehyde molecules, as well as the claisen condensation which is best known for the reaction between 2 thioesters acetyl thioester and malonyl thioester to form part of a fatty acid used in protein synthesis.
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.
SHYUKGHKY
1881
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.
Not really because aldol condensation of 2 CH3CHO would be a major competing process.
The Claisen-Schmidt reaction is a condensation reaction between an aldehyde or a ketone and an aromatic aldehyde that proceeds through the formation of an enolate ion from one of the carbonyl compounds. This enolate ion then attacks the carbonyl group of the aromatic aldehyde, leading to the formation of a β-hydroxy-α,β-unsaturated aldehyde or ketone. The reaction is typically base-catalyzed and proceeds via nucleophilic addition-elimination mechanism.
The key difference between the aldol and Claisen reactions in organic chemistry is the type of starting materials involved. In the aldol reaction, a carbonyl compound reacts with another carbonyl compound or an enolate ion to form a beta-hydroxy carbonyl compound. In the Claisen reaction, an ester reacts with a strong base to form a beta-keto ester. Both reactions involve the formation of new carbon-carbon bonds, but the aldol reaction involves carbonyl compounds while the Claisen reaction involves esters.
is a condensation reaction in which an amines are allowed to react with acids to form amides.first amine react with acid and form an amide.again formed amide reacts with an acid to form an second amide called benzimidazole[which has similar structure of benzene] it has basic nucleus of imidazole
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.
Rainer Ludwig Claisen died on 1930-01-05.
Rainer Ludwig Claisen was born on 1851-01-14.
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.