carboxylic acid reaction with bromine water


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  • Why do bromides react with -bromo carboxylic acids?

    Because bromides are capable of reacting with a wide variety of nucleophiles, α -bromo carboxylic acids serve as important intermediates. Reaction of α -bromo carboxylic acids with an aqueous basic solution followed by an acidic work-up produces α -hydroxy carboxylic acids.

  • What happens when carboxylic acid reacts with PBR 3?

    The reaction stats with the reaction of the carboxylic acid with PBr 3 to form the acid bromide and HBr. The HBr then catalyzes the formation of the acid bromide enol which subsequently reacts with Br 2 to give alpha bromination. Lastly, the acid bromide reacts with water to reform the carboxylic acid. Explain why the following reaction occurs.

  • Can a carboxylic acid be substituted with a bromine phosphorous tribromide?

    We could make an amino acid, starting from this carboxylic acid. This is a three carbon carboxylic acid. This is propanoic acid. If we react propanoic acid with, once again, a bromine phosphorous tribromide and then water, this is the HVZ reaction, which we know allows us to substitute the alpha position.

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