Aldol condensation - Wikipedia
网页An aldol condensation is a condensation reaction in organic chemistry in which two carbonyl moieties (of aldehydes or ketones) react to form a β-hydroxyaldehyde or β-hydroxyketone (an aldol reaction), and this is then followed by dehydration to give a conjugated enone.
Aldol Condensation - Chemistry LibreTexts
网页2023年1月23日 · An aldol condensation is a condensation reaction in organic chemistry in which an enol or an enolate ion reacts with a carbonyl compound to form a β-hydroxyaldehyde or β-hydroxyketone, followed by dehydration to give a conjugated enone.
Aldol Condensation - Mechanism, Crossed Aldol Condensation ...
网页Aldol condensation is an organic reaction in which an enolate ion reacts with carboxyl compound in order to form a β– hydroxy aldehyde or β– hydroxy ketone. Hydroxide functions as a base and therefore moves the acidic a …
Aldol Addition and Condensation Reactions – Master Organic ...
网页2022年4月14日 · The Aldol Addition reaction is the addition of an enolate to an aldehyde (or ketone). Heating with base can result in loss of water to give a new C-C pi bond, giving a product we refer to as the Aldol Condensation product. Similar reactions can proceed with the enolates of other species.
Aldol Condensation - Organic Chemistry Portal
网页Aldol Condensation. In some cases, the adducts obtained from the Aldol Addition can easily be converted (in situ) to α,β-unsaturated carbonyl compounds, either thermally or under acidic or basic catalysis. The formation of the conjugated system is the driving force for this spontaneous dehydration.
23.8: The Aldol Reaction and Condensation of Ketones and ...
网页Aldol Condensation: the dehydration of aldol products to synthesize α, β unsaturated carbonyls (enones) The products of aldol reactions often undergo a subsequent elimination of water, made up of an alpha-hydrogen and the beta-hydroxyl group.
The Complete Mechanism of an Aldol Condensation
网页2016年6月9日 · Although aldol condensation is one of the most important organic reactions, capable of forming new C–C bonds, its mechanism has never been fully established. We now conclude that the rate-limiting step in the base-catalyzed aldol condensation of benzaldehydes with acetophenones, to produce chalcones, is the final …
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