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 Multiple Choice QuestionsMultiple Choice Questions

621.

Ethylamine (C2H5NH2) can be obtained from N-ethipthalimide on treatment with

  • CaH2

  • H2O

  • NaBH4

  • NH2NH2


622.

Aniline dissolved in dilute HCl is reacted with sodium nitrite at 0ºC. This solution was added dropwise to a solution containing equimolar mixture of aniline and phenol in dil. HCl. The structure of the major product is


623.

The major product ‘Y’ in the following reaction is :


624.

Which of the following is NOT a correct method if the preparation of benzylamine from cyanobenzene ?

  • H2/ Ni

  • (i) LiAlH4

    (ii) H3O+

  • (i) SnCl2 + HCl(gas)

    (ii) NaBH4

  • (i) HCl/H2

    (ii) NaBH4


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625.

The correct statement regarding the basicity of arylamines is

  • Arylamines are generally more basic than alkylamines because the nitrogen lone pair electrons are not delocalized by interaction with the aromatic ring pi-electron system

  • Arylamines are generally more basic than alkylamines, because of aryl group

  • Arylamines are generally more basic than alkylamines because the nitrogen atom in arylamines is sp-hydridized.

  • Arylamines are generally more basic than alkylamines because the nitrogen atom in arylamines is sp-hydridized.

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626.

In the reaction,

straight H minus straight C identical to CH space rightwards arrow from left parenthesis ii right parenthesis space CH subscript 3 CH subscript 2 Br to left parenthesis straight i right parenthesis space NaNH subscript 2 divided by liq. NH subscript 3 of space straight X
space space space space space space space space space space space space space space space space space space straight X space rightwards arrow from left parenthesis ii right parenthesis space CH subscript 3 CH subscript 2 Br to left parenthesis straight i right parenthesis NaNH subscript 2 divided by liq. NH subscript 3 of space straight Y
X and Y are

  • X=2-butyne; Y= 3-hexyne

  • X=2-butyne;Y=2-hexyne

  • X=1-butyne ;Y = 2-hexyne

  • X=1-butyne ;Y = 2-hexyne

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627.

Consider the nitration of benzene using mixed conc. H2SO4 and HNO3. If a large amount of KHSO4 is added to the mixture, the rate of nitration will be

  • slower

  • uncharge

  • doubled

  • doubled

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628.

The product formed by the reaction of an aldehyde with a primary amine is

  • Ketone

  • Carboxylic acid

  • Aromatic acid

  • Aromatic acid

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629.

The electrolytic reduction of nitrobenzene in strongly acidic medium produces

  • p-aminophenol

  • azoxybenzene

  • azobenzene

  • aniline


A.

p-aminophenol

Under weakly acidic conditions nitrobenzene on electrolytic reduction gives aniline but under strongly acidic conditions gives p-aminophenol.

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630.

In the following reaction, the product (A) is 


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