amides can be formed by the reaction of which of the following?


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  • Why is the reaction between amines and carboxylic acids important?

    The reaction between amines and carboxylic acids to form amides is biologically important. It is through this reaction that amino acids (molecules containing both amine and carboxylic acid substituents) link together in a polymer to form proteins.

  • How amide hydrolysis occurs?

    Amides undergo hydrolysis to yield carboxylic acids plus ammonia or an amine upon heating in either aqueous acid or aqueous base. The conditions required for amide hydrolysis are more extreme than those required for the hydrolysis of acid chlorides or esters, but the mechanisms are similar.

  • How does amide ion deprotonate carboxylic acid?

    In the last step, the amide ion deprotonates the carboxylic acid to form a carboxylate salt and an amine as products. This final deprotonation step essentially removes the carboxylic acid from the equilibrium which drives the reaction towards completion.

Acid and base-catalyzed hydrolysis of amides  Organic chemistry  Khan Academy

Acid and base-catalyzed hydrolysis of amides Organic chemistry Khan Academy

Nomenclature and properties of amides  Organic chemistry  Khan Academy

Nomenclature and properties of amides Organic chemistry Khan Academy

Preparation of amides using DCC  Organic chemistry  Khan Academy

Preparation of amides using DCC Organic chemistry Khan Academy

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amine + hcl mechanism amine + koh amine acetic acid reaction amine acetylation mechanism amine alcohol condensation amine and acid chloride reaction amine and amino acid reaction amine and carboxylic acid reaction mechanism

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