The Hofmann rearrangement is a notable organic chemistry reaction that converts an amide into an amine with one less carbon atom. This process involves key steps such as bromination of nitrogen, extraction of H+ by OH-, and rearrangement of anion. The mechanism includes the formation of N-Bromoamide

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Aromatic rearrangements are key transformations in organic chemistry involving intramolecular and intermolecular rearrangements of aromatic systems. Examples include Fischer-Hepp rearrangement, Hofmann-Martius rearrangement, N-Azo to C-Azo rearrangement, Bamberger rearrangement, and Orton rearrangem

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This educational content delves into the classification and synthesis of amines, focusing on the synthesis of aliphatic amines through various methods like reduction of nitro compounds, acid amides, and aldoximes. It also discusses important reactions such as the Hofmann degradation, Curtius reactio

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