Nitrobenzene on treatment with zinc dust and aqueous ammonium chloride gives
C6H5N =N-C6H5
C6H5NH2
C6H5NO
C6H5NHOH.
Among the following which one does not act as an intermediate in Hofmann rearrangement?
RNCO
RCO
RCOHBr
RNC
Pyridine is less basic than triethylamine because
pyridine has aromatic character
nitrogen in pyridine is sp2 hybridised
pyridine is a cyclic system
in pyridine, lone pair of nitrogen is delocalised
Assertion: Anilinium chloride is more acidic than ammonium chloride.
Reason : Anilinium ion is resonance-stabilised.
If both assertion and reason are true and reason is the correct explanation of the assertion.
If both assertion and reason are true but reason is not the correct explanation of the assertion.
If assertion is true, but reason is false.
Both assertion and reason are false statements.
Hinsberg's reagent is :
B.
Benzene sulphonyl chloride is called Hinsberg's reagent. This reagent is used to distinguish between primary secondary and tertiary amines.
In the reaction :
C6H5CHO + C6H5NH2 C6H5N=HCC6H5 + H2O, the compound C6H5N=HCC6H5 is known as :
aldol
Schiffs base
Schiff's reagent
Benedict's reagent
IUPAC name of CH3-CH(CH2CH3)-CH2-CH(CN)-CH3 is :
2-cyano-3-methylhexane
2.4-dimethylhexanenitrile
3-methyl-5-cyanohexane
2-cyano-3-methylhexane
Aromatic nitriles (ArCN) are not prepared by reaction:
ArX + KCN
ArN2++ CuCN
ArCONH2+ P2O5
ArCONH2+ SOCl2
Melting points are normally the highest for
tertiary amides
secondary amides
primary amides
amines.