An Amine is best defined as a derivative of ammonia (NH3) where one or more N-H bonds are replaced by N-C bonds. Primary amines have one N-H bond replaced by a N-c bond, whereas secondary has two N-C bonds with one N-H bond and tertiary has all three N-C bonds making the molecular formula NC3. An amide is a nitrogen bonded to a carbonyl group.
amide is carbonyl group with nitrogen
and an amine is RNH2 (general formula) although u could get primary, secondary and tertiary amines. where the number of hydrogens reduce by one respectively.
In amines R-NH2 the lone pair of nitrogen is available for attack of an acid so it is a base but in amides R-CO-NH2 the lone pair of nitrogen becomes involved in resonance process due to electrons attracting effect of oxygen and is not available for the attack of an acid so it is not basic, the resonance effect produces positive charge on nitrogen atom so it may remove hydrogen ion and may acts as an acid.
Aliphatic amines has no aromatic ring while aromatic amines have the nitrogen atom connected to them.
A special amide bond that forms between the amine group and the hydroxyl group on amino acids.
Oh yeah, gotta love a good question about urine. Urea has the structure of an Amide.
The functional groups present in caffeine are alkene, amide, and amine.
This is the group amine.
An amine is a functional group while an ammine complexes are metal complexes containing at least one ammonia (NH3) ligand. "Ammine" is spelled this way due to historical reasons
Poly-amines are more durable, poly-amides are more resistant to moisture.
Amine.
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
A special amide bond that forms between the amine group and the hydroxyl group on amino acids.
Oh yeah, gotta love a good question about urine. Urea has the structure of an Amide.
Amide on heating.
An amidification is the formation of an amide from a carboxylic acid by reaction with an amine.
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.
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.
The amine group because it means nitrogen-containing, and nitrogen is indeed the essential componenet of the amine portion of the molecule.