Nitrites are reduced to primary amines with the help of
Pt
NaH2
LiAlH4
H2O
Due to the presence of unshared electron pair, amines behave as
Electrophiles
Anions
Nucleophiles
Cation
The simplest arylamine is known as
Benzene
Phenine
Ethamine
Aniline
The reaction which is used as a test for primary amines
Carbylamine reaction
Gaberial synthesis
Hoffmann bromamide reaction
Salphonation
Amides on reduction with Lithium Aluminium hydride gives
Amino acids
Amines
Alkanes
Alkenes
When diazonium salt is allowed to rise up to 283 K, the salt gets hydrolysed to
Alcohol
Arenes
Amides
Phenol
Sulphanilic acid is
P-aminobenzene sulphonic acid
M-aminobenzene sulphonic acid
Anilinium hydrogen sulphate
Nitroaufanilide
The conversation of primary aromatic amines into diazonium salt is known as
Alkylation
Arylation
Diazotisation
Acetylation
In Gattermann reaction, the reaction mixture combines with
Cu(I)ion
Cu(II)ion
Cu
Cyanide ion
The hybridisation of nitrogen in amines
Sp2
Sp
Sp3
Sp3d