Amides on reduction with Lithium Aluminium hydride gives
Amino acids
Amines
Alkanes
Alkenes
Aniline reacts with bromine water at room temperature to give a white precipitate of
2-bromoaniline
2,4,6-tribromoaniline
4-bromoaniline
3-bromoaniline
A tertiary amino compound which is a well known antihistaminic drug
Benadryl
Novocain
Paracetamine
Acetophenanine
In trimethylamine, the C-N-E bond angle is
118.50
1030
109.50
1080
Amines react with benzoyl chloride. This reaction is called
Alkylation
Arylation
Catenation
Benzoylation
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
Benzene diazonium salt is
C6H5NH2Cl
C6H5N2HCl2
C6H5N2Cl
C6H5NO2Cl
Sulphanilic acid is
P-aminobenzene sulphonic acid
M-aminobenzene sulphonic acid
Anilinium hydrogen sulphate
Nitroaufanilide
Ethanol and hydrogen
Ethanolic HCN
Ethanolic NaCN
HCN/HCl