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What is HVZ reaction?
Treatment with bromine and a catalytic amount of phosphorus leads to the selective α-bromination of carboxylic acids.
Phosphorus reacts with bromine to give phosphorus tribromide, and in the first step this converts the carboxylic acid into an acyl bromide.
An acyl bromide can readily exist in the enol form, and this tautomer is rapidly brominated at the α-carbon. The monobrominated compound is much less nucleophilic, so the reaction stops at this stage. This acyl intermediate compound can undergo bromide exchange with unreacted carboxylic acid via the anhydride, which allows the catalytic cycle to continue until the conversion is complete.
read less
Treatment with bromine and a catalytic amount of phosphorus leads to the selective α-bromination of carboxylic acids.
Phosphorus reacts with bromine to give phosphorus tribromide, and in the first step this converts the carboxylic acid into an acyl bromide.
An acyl bromide can readily exist in the enol form, and this tautomer is rapidly brominated at the α-carbon. The monobrominated compound is much less nucleophilic, so the reaction stops at this stage. This acyl intermediate compound can undergo bromide exchange with unreacted carboxylic acid via the anhydride, which allows the catalytic cycle to continue until the conversion is complete.
read lessThe Hell–Volhard–Zelinsky halogenation reaction halogenates carboxylic acids at the α carbon. The reaction is named after three chemists, the German chemists Carl Magnus von Hell (1849–1926) and Jacob Volhard(1834–1910) and the Russian chemist Nikolay Zelinsky (1861–1953)
read lessHvz means Hell-Volhard-Zelinsky Reaction. It is an ORGANIC MECHANISM in which the PHOSPHORUS reacts with BROMINE to give PHOSPHORUS TRI BROMIDE, and in the first step this converts the carboxylic acid into an acyl bromide. An acyl bromide can readily exist in the enol form, and this tautomer is rapidly.
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