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101.

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.


102.

Hinsberg's reagent is :


103.

In the reaction :

C6H5CHO + C6H5NH2  C6H5N=HCC6H5 + H2O, the compound C6H5N=HCC6H5 is known as :

  • aldol

  • Schiffs base

  • Schiff's reagent

  • Benedict's reagent


104.

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


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105.

Aromatic nitriles (ArCN) are not prepared by reaction:

  • ArX + KCN

  • ArN2++ CuCN

  • ArCONH2+ P2O5

  • ArCONH2+ SOCl2


106.

Melting points are normally the highest for

  • tertiary amides

  • secondary amides

  • primary amides

  • amines.


107.

Assertion: Boiling and melting points of amides are higher than corresponding acids.
Reason: It is due to strong intermolecular hydrogen bonding in their molecules.

  • If both assertion and reason are true and the reason is a correct explanation of the assertion.

  • If both the assertion and reason are true but the reason is not a correct explanation of the assertion.

  • If the assertion is true but the reason is false.

  • If both the assertion and reason are false.


108.

The basicity of aniline is weaker in comparison to that of methylamine due to:

  • hyper conjugative effect of Me-group in MeNH2

  • resonance effect of the phenyl group in aniline

  • the lower molecular weight of methylamine as compared to that of aniline

  • resonance effect of -NH2 group in MeNH2


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109.

An amine C3H9N reacts with benzene sulphonyl chloride to form a white precipitate which is insoluble in aq. NaOH. The amine is


110.

The reaction of aniline with chloroform under alkaline conditions leads to the formation of 

  • phenylcyanide

  • phenylisonitrile

  • phenylcyanate

  • phenylisocyanate


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