In organic chemistry, enolates are organic anions derived from the deprotonation of carbonyl (RR'C=O) compounds. Rarely isolated, they are widely used as reagents in the synthesis of …

Aug 16, 2022 · Enolates can be formed through removing the proton on carbons adjacent to a carbonyl (i.e. the “ alpha-carbon “). The resulting anions are much more stable than typical …

Since the negative charge of an enolate anion is delocalized over the alpha-carbon and the oxygen, as shown earlier, electrophiles may bond to either atom. Reactants having two or …

An enolate is a resonance-stabilized anion formed during the base-catalyzed tautomerization of carbonyl compounds. The process begins when a base removes an alpha proton (a hydrogen …

Enolates are resonance-stabilized anions that play a crucial role in organic chemistry as versatile nucleophiles. Understanding their formation, reactions, and applications is essential for …

Enolates, or oxyallyl anions, are versatile reagents for the formation of α-substituted carbonyl compounds and are therefore important intermediates for the synthesis of complex molecules.

Apr 16, 2025 · Enolates are reactive intermediates in organic chemistry that play a central role in forming carbon–carbon bonds. They are formed by deprotonating the α-hydrogen of carbonyl …

Apr 22, 2024 · One of the main characteristics of the carbonyl group is that the hydrogens adjacent to the carbonyl carbon are acidic and can react with certain bases. If this occurs, the …

Jun 9, 2025 · Enolates are versatile nucleophiles that participate in a variety of reactions, forming new carbon-carbon bonds and introducing functionality into molecules.

Feb 26, 2024 · Under neutral or acidic conditions, it can exist in the enol form, which is nucleophilic through the adjacent carbon atom. Under basic conditions, it is converted to an …