Aza-Claisen Rearrangement:

The Aza-Claisen rearrangement is a chemical reaction involving a nitrogen atom’s migration from one position to another within a molecule. It is named after the Claisen rearrangement, a well-known rearrangement reaction involving oxygen atoms. The mechanism of the aza-Claisen rearrangement: The mechanism of the aza-Claisen rearrangement involves three steps:  Protonation: The reaction often starts with … Read more

Schmidt Reaction (Rearrangement): definition| Mechanism| example

Schmidt Reaction for Synthesis of Nitrile and Amide

Schmidt reaction is a acid-catalyzed Rearrangement reaction of hydrazoic acid reactions of electrophiles, like carbonyl compounds, alkenes tertiary and alcohols. The following these substrates include amines, nitriles, amides or imines, rearrangement and extrusion of nitrogen.

Favorskii Rearrangement


What is Favorskii Rearrangement explain? Favorskii Rearrangement is organic reaction of α-halo ketones (chlorine, bromine, or iodine) having at least one α-hydrogen, with a nucleophile (alcohol, amine, or H2O) in the presence base (usually an alkoxide or hydroxide) give carboxylic acids or carboxylic acid derivatives via a cyclopropanone intermediate. It is widely used organic reaction … Read more

Dakin Oxidation Reaction : Definition | Mechanism | Examples

Definition : In Dakin oxidation, aromatic aldehydes or ketones undergo treatment with RCO3H or H2O2 to smoothly oxidize them into carboxylic acids. The reaction operates effectively when the aromatic aldehyde or ketone possesses electron-rich (-R, -OH, -OR, -NH2, or -NHR) substituents in the para or ortho positions. When the aromatic ring is substituted with electron-withdrawing … Read more