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When a carboxylic acid and an amine react, they form an amide through a condensation reaction. This reaction involves the loss of a water molecule and the formation of a new C-N bond between the carbonyl carbon of the carboxylic acid and the amino nitrogen of the amine.

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Q: When a carboxylic acid and an amine react they form a?
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Why can 6-aminohexanoic acid undergo a polymerization reaction with itself?

6-aminohexanoic acid contains two functional groups, an amine group and a carboxylic acid group, that can react with each other. When these functional groups react, they form amide linkages, resulting in the formation of a polymer through a process known as polyamide synthesis.


What is the Reaction with carboxylic acid and metal acids?

When carboxylic acids react with metal hydroxides, they form metal carboxylates and water through a neutralization reaction. This process involves the transfer of a proton from the carboxylic acid to the metal hydroxide, leading to the formation of the salt (metal carboxylate) and water as a byproduct.


Is a sodium fatty acid salt the same as a carboxylic acid salt?

Yes, a sodium fatty acid salt is a type of carboxylic acid salt. Fatty acids are carboxylic acids with long hydrocarbon chains, and when they react with a base like sodium hydroxide, they form carboxylic acid salts such as sodium fatty acid salts.


Identify two compounds which react together to form a ester?

An alcohol (such as ethanol) and a carboxylic acid (such as acetic acid) can react together in the presence of an acid catalyst to form an ester, with water as a byproduct. This reaction is known as esterification.


Why does chromic acid react with aldehydes?

Chromic acid (H2CrO4) reacts with aldehydes to form carboxylic acids through oxidation. This reaction involves the transfer of oxygen to the aldehyde carbon, converting it to a carboxylic acid functional group.

Related questions

An amine and a carboxylic acid react to form water and?

Amide on heating.


What are the two functional groups that react to form nylon?

The two functional groups that react to form nylon are an amine group (-NH2) and a carboxylic acid group (-COOH). These groups undergo a condensation reaction to form an amide bond, resulting in the polymer known as nylon.


Why can 6-aminohexanoic acid undergo a polymerization reaction with itself?

6-aminohexanoic acid contains two functional groups, an amine group and a carboxylic acid group, that can react with each other. When these functional groups react, they form amide linkages, resulting in the formation of a polymer through a process known as polyamide synthesis.


Does potassium oxide react with a carboxylic acid?

Yes, they react tor form water and the corresponding potassium carboxylate salt.


What is the Reaction with carboxylic acid and metal acids?

When carboxylic acids react with metal hydroxides, they form metal carboxylates and water through a neutralization reaction. This process involves the transfer of a proton from the carboxylic acid to the metal hydroxide, leading to the formation of the salt (metal carboxylate) and water as a byproduct.


Is a sodium fatty acid salt the same as a carboxylic acid salt?

Yes, a sodium fatty acid salt is a type of carboxylic acid salt. Fatty acids are carboxylic acids with long hydrocarbon chains, and when they react with a base like sodium hydroxide, they form carboxylic acid salts such as sodium fatty acid salts.


What common characteristics do all amino acids have?

Their base. A ionized in solution amine group attached to a central chiral carbon, which is attached to a variable R group, a hydrogen and a carboxylic acid, which is the ionized form of a carboxyl group.


Can carboxylic acid react with grignard reagent?

Yes, carboxylic acids can react with Grignard reagents to form a variety of products, including ketones and alcohols. The reaction typically involves the addition of the Grignard reagent to the carbonyl carbon of the carboxylic acid, followed by protonation to give the desired product.


Identify two compounds which react together to form a ester?

An alcohol (such as ethanol) and a carboxylic acid (such as acetic acid) can react together in the presence of an acid catalyst to form an ester, with water as a byproduct. This reaction is known as esterification.


Is esterfication a substitution or addition reaction?

Esterification is a type of substitution reaction where an alcohol and carboxylic acid react to form an ester and water. This reaction involves the substitution of the hydroxyl group of the carboxylic acid with an alkoxy group from the alcohol.


Why does chromic acid react with aldehydes?

Chromic acid (H2CrO4) reacts with aldehydes to form carboxylic acids through oxidation. This reaction involves the transfer of oxygen to the aldehyde carbon, converting it to a carboxylic acid functional group.


What product wil form when Anthranilic acid reacts with ethanol amine in presence of sulfuric acid?

Anthranilic acid + ethanol amine C6H4(NH2)COOH + OHCH2CH2NH2 = C6H4(NH2)COOCH2CH2NH2 + H2O Sulphuric acid(H2SO4) is an acid catalyst which deprotonates the carboxylic group(COOH) of anthranilic acid and removes the hydroxy(OH) group from ethanol amine. The (H+) proton then attaches to the (-OH) to form water(H2O) as a byproduct. The deprotonated carboylate(COO-) group of anthranilic acid then attaches to the the (+CH2CH2NH2) to form the amide/ester product. The structure is amine (NH2 bonded to benzene ring) with (COOCH2CH2NH2) bonded to the ortho position of the benzene ring