The reaction described here is the Aldol Condensation. It involves the reaction of two aldehydes or a ketone and an aldehyde, where one of the carbonyl compounds undergoes an enolate formation followed by nucleophilic attack on another carbonyl group, leading to the formation of a β-hydroxy ketone or aldehyde (aldol product), which then undergoes dehydration to form an α,β-unsaturated carbonyl compound.
- Aldol Condensation: This reaction is a combination of two carbonyl compounds (benzaldehyde and acetophenone) that form a new carbon-carbon bond and lead to the formation of Benzalacetophenone.
- Friedel-Crafts Acylation: This reaction involves the acylation of an aromatic compound using an acyl halide and a Lewis acid like AlCl₃.
- Claisen Condensation: This is a reaction of esters with base to form β-keto esters or β-diketones.
- Benzoin Condensation: This involves the reaction of aromatic aldehydes to form a benzoin product.
Thus, Aldol Condensation is the correct name for the reaction.