Wurtz-Fittig reaction
Step 1: The Hell-Volhard-Zelinsky reaction specifically involves the halogenation of the alpha-carbon of carboxylic acids.
Step 2: This reaction uses a halogen (Br\(_2\)) and red phosphorus, which generates phosphorus tribromide (PBr\(_3\)), acting as a catalyst.
Step 3: Phosphorus tribromide converts the carboxylic acid to an acyl bromide, which subsequently undergoes alpha-bromination.
Step 4: The product, 2-bromopropanoic acid, confirms the pathway and mechanism of the Hell-Volhard-Zelinsky reaction.