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 Multiple Choice QuestionsMultiple Choice Questions

121.

The strained tetracyclic alkane is isomerize thermally to the cyclic alkene. The reaction involves

  • free radical

  • carbocation

  • carbanion

  • carbene.


122.

How much amount of CuSO4.5H2O is required for liberation of 2.54 g of I2 when titrated with KI?

  • 2.5 gm

  • 4.99 gm

  • 2.4 gm

  • 1.2 gm


123.

Which of the following conditions is not correct for resonating structures?

  • The contributing structures must have the same number of unpaired electrons.

  • The contributing structures should have similar energies.

  • The contributing structures should be so written that unlike charges reside on atoms that are far apart.

  • The positive charge should be present on the electropositive element and the negative charge on the electronegative element.


124.

+ I effect is shown by :

  • -CH3

  • -Br

  • -Cl

  • -NO2


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125.

How many chiral carbonatoms are present in 2 , 3 , 4 - trichloropentane ?

  • 4

  • 1

  • 2

  • 3


126.

Decreasing order of nucleophilicity is

  • OH- > NH2- > CH3O- > RNH2

  • NH2- > OH- > CH3O- > RNH2

  • NH2- > CH3O- > OH- > RNH2

  • CH3O- > NH2- > OH- > RNH2


127.

Find the number of stereoisomers of 1,2-dihydroxy cyclopentane.

  • 1

  • 2

  • 3

  • 4


128.

Best method to form aromatic iodide is

  • ArN2+ + KI 

  • RNH2 + I2 

  • ArN2+ + KI 

  • ArN2+ + PI3 


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129.

Which is optically inactive?


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130.

Assertion : C(CH3)3-CH2-Br + NaOH C(CH3)2OH-CH2-CH3

Reason : It follows with formation of more stable carbocation.

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

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

  • If assertion is true but reason is false

  • If both assertion and reason are false.


A.

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

Neopentyl bromide being primary alkyl halide does not undergo SN2 reaction but proceeds via SN1 path because of steric hindrance caused by the bulky nature of tertiary butyl group.


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