Important Questions of Amines Chemistry | Zigya

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511.

0ne mole of hydrazine (N2H4) loses 10 moles of electrons in a reaction to form a new compound X. Assuming that all the nitrogen atoms in hydrazine appear in the new compound, what is the oxidation state of nitrogen in X? (Note - There is no change in the oxidation state of hydrogen in the reaction).

  • -1

  • -3

  • +3

  • +5


512.

Which one of the following is used as a test for aliphatic primary amines?

  • Tollen's test

  • Fehling's test

  • lsocyanide test

  • Azo dye test


513.

When methanamine is treated with benzoyl chloride, the major product is

  • N-phenylethanamide

  • N-methylbenzamide

  • benzanilide

  • acetophenone


514.

Phenyl isocyanide is prepared from aniline by

  • Carbylamine reaction

  • Rosenmund's reaction

  • Koble's reaction

  • Reimer-Tiemann reaction


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515.

Gabriel's phthalimide synthesis can be used to prepare

  • ethanamine

  • N-methylmethanamine

  • benzene amine

  • N, N-dimethylmethanamine


516.

Select the compound which on treatment with nitrous acid liberates nitrogen.

  • Nitroethane

  • Triethylamine

  • Diethylamine

  • Ethylamine


517.

The compound that neither forms semicarbazone nor oxime is

  • HCHO

  • CH3COCH3

  • CH3CHO

  • CH3CH2CH2NH2


518.

Positive carbylamine test is shown by

  • N, N-dimethylaniline

  • triethylamine

  • N-methylaniline

  • p-methylbenzylamine


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519.

Ethanoic acid on heating with ammonia forms compound A which on treatment with bromine and sodium hydroxide gives compound B. Compound B on treatment with NaNO3/dil.HCl gives compound C. The compounds A, B and C respectively are

  • ethanamide, methanamine, methanol

  • propanamide, ethanamine, ethanol

  • N-ethylpropanamide, methaneisonitrile, methanamine

  • ethanamine, bromoethane, ethanediazoniumchloride


520.

n-butylamine (l),  diethylamine (II) and N,  N-dimethylethylamine (III)  have the same molar mass.  The increasing order of their boiling point is

  • III < II < I

  • I < II < III

  • II < III < I

  • II < I < III


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