To aniline, we add Sulphuric acid at 180.C. This will give us Sulphanilic acid.
C6H5NH2+H2SO4-------->C6H5 NH3+HSO4-------455 to 475.K----->
C6H5NH2SO3H <=>C6H5NH3+SO3- (zwitter ion)
Obviously its acid, because its name is acid
To prepare phenyl benzoate from phenol, first convert phenol to phenyl benzoate by reacting it with benzoic acid and a catalyst such as concentrated sulfuric acid or concentrated hydrochloric acid at elevated temperatures. This esterification reaction will yield phenyl benzoate along with water as a byproduct. Purification techniques such as distillation can then be used to isolate the desired product.
The R-group in the phenylalanine amino acid is: CH2-benzene ring
Phenyl salicylate does not form a polar covalent bond. It is an ester that consists of a benzene ring (phenyl group) and salicylic acid. The bond between the benzene ring and the carboxyl group in salicylic acid is a typical ester covalent bond.
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.
Obviously its acid, because its name is acid
To prepare phenyl benzoate from phenol, first convert phenol to phenyl benzoate by reacting it with benzoic acid and a catalyst such as concentrated sulfuric acid or concentrated hydrochloric acid at elevated temperatures. This esterification reaction will yield phenyl benzoate along with water as a byproduct. Purification techniques such as distillation can then be used to isolate the desired product.
It is an organic acid where a -SO3H functional group is attached to a benzene ring.
Phenyl acetate is less polar than butyric acid. This is because butyric acid has more polar functional groups present (carboxylic acid) compared to phenyl acetate (ester).
Its common name is B- phenyl butyric acid (B=Beta)
The ingredients that are in a Tide to Go pen are water, alkyl amine oxide, dipropylene glycol phenyl ether, hydrogen peroxide and citric acid. It also contains ethylene diamine disuccinic acid, sodium salt, sodium alkyl sulfate and fragrances.
Salts in amine solutions are formed through the reaction of amines with acids. When an amine, which is a basic compound, reacts with an acid, it accepts a proton (H+) from the acid, resulting in the formation of an ammonium ion. This ammonium ion then combines with the anion from the acid, leading to the formation of an amine salt. The process is an example of acid-base neutralization, where the amine acts as a base.
The R-group in the phenylalanine amino acid is: CH2-benzene ring
First off, if it has Phenyl in it, it is a poison
Amine.
Aniline can be converted into phenyl hydrazine by reacting it with hydrazine hydrate in the presence of an acid catalyst such as hydrochloric acid. The reaction proceeds through the formation of a diazonium salt intermediate, which then reacts with excess hydrazine to form phenyl hydrazine.
The carbohydrate that has a sugar acid and sugar amine disaccharide repeat unit are called heteropolysaccharides.