The document summarizes the aldol condensation reaction of benzaldehyde and acetone to produce dibenzalacetone. It involves generating the acetone enolate ion using a strong base. The enolate then reacts with benzaldehyde through an E1CB mechanism to form the product. The reaction is performed in water/ethanol with sodium hydroxide and produces the trans, trans isomer of dibenzalacetone as the exclusive product. Stirring and controlling temperature and base concentration are important for obtaining the desired product.

1. prepared by. Aram Ishmael Bakhan Ibrahim 3 rd stage –chem.dept. Sulaimani uni.

4. Being a very strong nucleophile, this enolate attacks the carbonyl of benzaldehyde and forms a B-carbonyl alkoxide ion. This alkoxide ion abstracts a proton from water to form a beta hydroxy ketone. Sodium hydroxide abstracts another acidic alpha H to form a stabilized carbanion. The electron pair on carbon is used to eliminate the hyroxide ion, forming a alpha-beta unsaturated ketone in an irreversible step. This is an example of an E1CB mechanism. Note that in this reaction, the intermediate alcohol is dehydrated under basic conditions, unlike most alcohol dehydrations, which are generally E1 mechanisms under acid conditions. The E1CB mechanism is made possible by the presence of the carbonyl, which stabilizes the intermediate carbanion

5. Since this newly formed ketone still posses alpha hydrogens, it too can undergo the same enolate condensation reaction with a second mole of benzaldehyde to form the final product: