alcoholate

the reaction was carried out with an alcoholate as the nucleophile.

lithium aluminum hydride is a strong reducing agent that can reduce esters to alcohols using an alcoholate.

the alcoholate anion acts as a base in many organic reactions.

alcoholates are often used to deprotonate carboxylic acids.

the alcoholate can be prepared by reacting an alcohol with a strong base.

alcoholates are versatile reagents in organic synthesis.

the reaction mechanism involves the nucleophilic attack of an alcoholate on an electrophile.

alcoholates can be used to form ethers through williamson ether synthesis.

the stability of an alcoholate depends on the nature of the alkyl group.

alcoholates are typically strong bases and can react with water to form alcohols and hydroxides.