Rosenmund Reduction
The Rosenmund Reduction reaction is a hydrogenation process in which an acyl chloride is selectively reduced to an aldehyde. The reaction was named after Karl Wilhelm Rosenmund who discovered it …
The Rosenmund Reduction reaction is a hydrogenation process in which an acyl chloride is selectively reduced to an aldehyde. The reaction was named after Karl Wilhelm Rosenmund who discovered it …
The Haloform Reaction is an organic chemical reaction where a haloform (CHX3, where X is a halogen) is produced by the exhaustive halogenation of a methyl ketone (RCOCH3, where R …
SN2 Reaction is a Nucleophilic Substitution reaction (A class of reactions wherein the electron-rich nucleophile attacks a positively charged electrophile to replace a leaving group) in which two components are …
SN1 Reaction is a Nucleophilic Substitution reaction (A class of reactions wherein the electron-rich nucleophile attacks a positively charged electrophile to replace a leaving group) in which the rate-determining step …
Etard Reaction is the partial oxidation of an aromatic ring with an attached methyl group. For example, converting Toluene (C7H8– A hexagon with a methyl group-CH3) into aldehydes like Benzaldehyde (C7H6O …
Wurtz Reaction is an organic coupling reaction in organic and organo-metallic chemistry which is named after Charles Adolphe Wurtz . This reaction is also known as Wurtz coupling. It is …
Swarts Reaction is an organic reaction in which alkyl chlorides/alkyl bromides are usually converted to alkyl fluorides. This process was described by Frederick Jean Edmond Swarts in 1892. This reaction …
The Finkelstein Reaction is an organic SN2 Reaction(substitution nucleophilic bimolecular reaction) which is named after the German chemist Hans Finkelstein. This reaction involves the exchange of one halogen atom for another. …
The Gattermann reaction is as an organic chemical reaction in which Aromatic compounds are formylated by a mixture of hydrogen cyanide and hydrochloric acid(HCL) in the presence of a Lewis …