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Stephen Reduction Reaction is also known as Stephen aldehyde synthesis or Stephen reaction in organic chemistry. here is the Stephen Aldehyde Synthesis Mechanism and Application. here aliphatic or aromatic nitrile is converted to imidoyl chloride or uses of sulphuric acid by using hydrochloric acid and further to aliphatic or aromatic aldehyde. Sandmeyer Reaction: Definition| Mechanism| … Read more
The formylation of electron-rich aromatic compounds with a mixture of dimethylformamide and phosphorus oxychloride POCl3 is commonly referred to as the Vilsmeier reaction, or sometimes the Vilsmeier-Haack reaction, from the names of the two German chemists who first described it in 1927.
here we will discuses about mechanism and examples of Chugaev Elimination Reaction. chugaev elimination pdf, chugaev reaction slideshare, chugaev reaction ppt.
The Sandmeyer reaction is an organic substitution type reaction used for the synthesis of aryl halide from an aryl diazonium salt. the catalyst used in Sandmeyer reaction is a copper(I) halide like chloride, bromide or iodide ions catalyst. significantly, The reaction include trifluoromethylation, hydroxylation, cyanation, and halogenation type reaction on benzene.
The most well-known use of the Strecker reaction, α-amino nitriles, is their hydrolysis under acidic or basic conditions to obtain α-amino acids (Strecker amino acid synthesis).
The Perkin reaction (or Perkin condensation) is an condensation of aromatic aldehydes and the anhydrides of aliphatic carboxylic acids in the presence of a weak base to obtain α,β-unsaturated carboxylic acids