Subject

Chemistry

Class

JEE Class 12

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 Multiple Choice QuestionsMultiple Choice Questions

41.

The brown ring test for nitrates depends on :

  • the reduction of nitrate to nitric oxide

  • oxidation of nitric oxide to nitrogen dioxide

  • reduction of ferrous sulphate to iron

  • oxidising action of sulphuric acid


42.

An organic compound which produces a bluish green coloured flame on heating in presence of copper is :

  • chlorobenzene

  • benzaldehyde

  • aniline

  • benzoic acid


43.

For a reaction A+ B → C + D if the concentration of A is doubled without alterning the concentration of B, the rate gets doubled. If the concentration of B is increased by nine times without alterning the concentration of A, the rate gets tripled. The order of the reaction is :

  • 2

  • 1

  • 3/2

  • 4/3


44.

Methyl bromide is converted into ethane by heating it in ether medium with :

  • Al

  • Zn

  • Na

  • Cu


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45.

The catalyst used in the preparation of an alkyl chloride by the action of dry HCl on an alcohol is:

  • anhydrous AlCl3

  • FeCl3

  • anyhydrous ZnCl2

  • Cu


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46.

Which of the following compound would not evolve CO2 when treated with NaHCO3 solution?

  • Salicylic acid

  • Phenol

  • Benzoic acid

  • 4-nitrobenzoic acid


B.

Phenol

Phenol does not decompose sodium carbonate or sodium bicarbonate i.e., CO2 is not evolved, because phenol is a weaker acid than carbonic acid.


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47.

Identify the product Y in the following reaction sequence:

  • pentane

  • cyclobutane

  • cyclopentane

  • cyclopentanone


48.

The reaction C2H5ONa + C2H5I → C2H5OC2H5 + NaI is known as:

  • Kolbe's synthesis

  • Wurtz's synthesis

  • Williamson's synthesis

  • Grignard's synthesis


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49.

The basicity of aniline is less than that of cyclohexylamine. This is due to :

  • +R-effect of-NH2 group

  • -I effect of -NH2 group

  • -R effect of-NH2 group

  • hyperconjugation effect


50.

Which of the following compound is expected to be optically active?

  • (CH3)2CHCHO

  • CH3CH2CH2CHO

  • CH3CH2CHBrCHO

  • CH3CH2CBr2CHO


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