Take This Quiz On Named Reactions!

An organic reaction in which an enolate ion reacts with a carbonyl compound to form β-hydroxy ketone, to give a conjugated enone.

The reaction showcases the conversion of arylamines to aryl fluorides.

The chemical reaction signifies the base-induced disproportionation of a non-enolizable aldehyde.

Which of the following shows how to reduce ketones or aldehydes to alkanes using zinc amalgam and hydrochloric acid.

A chemical reaction in which a heterocyclic bound or an aromatic methyl group is directly oxidized to an aldehyde using chromyl chloride.

The Friedel – Crafts Reaction is a way of attaching substituents to an aromatic ring.

The __________ reaction is used for the conversion of a primary amide to a primary amine with one less carbon atom.

Which reaction is used for the halogenation of carboxylic acids at the alpha carbon?

A chemical reaction where haloforms are produced by the exhaustive halogenation of methyl aldehyde or methyl ketone with a base present.

The Carbylamine reaction is also known as Fischer Esterification synthesis.

This is a named reaction in organic chemistry involving obtaining methylene groups by converting carbonyl functionalities.

Name the chemical reaction that helps in forming an ether from an organohalide and deprotonated alcohol.

________ is a chemical reaction in which we use aryl diazonium salts to synthesize aryl halides.

A hydrogenation process in which an acyl chloride is selectively reduced to an aldehyde.

Which reaction is used for the ortho-formylation of phenols?

Name the chemical reaction that is used to obtain primary amines from primary alkyl halides.

In which chemical reaction the aromatic hydroxy acid is produced?

During the Stephen Reaction, ammonium chloride is also produced.

_________ and Finkelstein reactions are halogen exchange reactions that are associated with alkyl halides.

Does Fischer Esterification an organic reaction?