Neither.
Aspirin, acetyl salicylic acid, is a structure containing benzene, carboxylic acid, and ester functional groups, but it does not contain nitrogen at all, let alone eitehr an amine or amide.
Amide on heating.
An amidoamine is any amine which also has an amide group, typically a monoamide of a diamine.
When an amine is combined (reacted) with a carboxyl group, an AMIDE + water is formed, and if you carry on heating under a vacuum, an imidazoline is formed.
The amine group because it means nitrogen-containing, and nitrogen is indeed the essential componenet of the amine portion of the molecule.
Esters and amides are derivatives of carboxylic acids. Amines are alkylated derivatives of ammonia: carboxylic acid= R-COOH ester= R-COOR amide=R-CONH2 amine= R-NHR
Amine.
Oh yeah, gotta love a good question about urine. Urea has the structure of an Amide.
An amidification is the formation of an amide from a carboxylic acid by reaction with an amine.
Amide on heating.
An amidoamine is any amine which also has an amide group, typically a monoamide of a diamine.
The functional groups present in caffeine are alkene, amide, and amine.
When an amine is combined (reacted) with a carboxyl group, an AMIDE + water is formed, and if you carry on heating under a vacuum, an imidazoline is formed.
A special amide bond that forms between the amine group and the hydroxyl group on amino acids.
The amine group because it means nitrogen-containing, and nitrogen is indeed the essential componenet of the amine portion of the molecule.
They are amide bonds -covalent. When an amino acid reacts with another, the carboxylic acid reacts with the amine forming an amide.
N in the amine group. N in the amide group is stabilized thru resonance=less basic
Native amide bonds take part in formation of a peptide. If the amine and carboxylic acid functional groups in amino acids join together to form amide bonds, a chain of amino acid units is formed, thus called the peptide bonds.Ê