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 Multiple Choice QuestionsMultiple Choice Questions

91.

Rate determining step in nitration of benzene is

  • formation of NO2+

  • formation of carbocation

  • replacement of H atom

  • none of these.


92.

1,4-dimethylbenzene on heating with anhydrous AlCl3 and HCl produces

  • 1, 2-dimethylbenzene

  • 1, 3-dimethylbenzene

  • 1, 2, 3-trimethylbenzene

  • ethylbenzene


93.

In 2-butene, which one of the following statements is true?

  • C1-C2 bond is sp3-sp3 -σ-bond

  • C2-C3 bond is sp3-sp2 -σ-bond

  • C1-C2 bond is an sp3-sp2 -σ-bond

  • C1-C2 bond is an sp2-sp2 -σ-bond


94.

The stability of Me2C=CH2 is more than that of MeCH2CH=CH2 due to:

  • inductive effect of the Me groups

  • resonance effect of the Me groups

  • hyperconjugation effect of the Me groups

  • resonance as well as the inductive effect of the Me groups


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95.

Friedel-Craft's reaction using MeCl and anhydrous AlCl3 will take place most efficiently with:

  • benzene

  • nitrobenzene

  • acetophenone

  • toluene


96.

The 4th higher homologue of ethane is

  • butane

  • pentane

  • hexane

  • heptane


97.

The ease of nitration of the following three hydrocarbons follows the order:

  • II = III = I

  • II > III > I

  • III > II > I

  • I = III > II


98.

Among the alkenes which one produces tertiary butyl alcohol on acid hydration?

  • CH3-CH2-CH=CH2

  • CH3-CH=CH-CH3

  • (CH3)2C=CH2

  • CH3-CH=CH2


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99.

The most likely protonation site in the following molecule is

  • C-1

  • C-2

  • C-3

  • C-6


A.

C-1

Addition of a proton at C1 results in the formation of tropylium carbocation (i.e. an aromatic species with more stability due to delocalisation of π electrons), thus, it is the most reactive site towards protonation.

Addition of proton. at any other carbon atom, interupt in the delocalisation of π electrons by disturbing planarity of molecules and hence, makes it less stable. Thus, these all are less reactive towards protonation.


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100.

The structure of isobutyl group in an organic compound is

  • C2H6-CH-CH2-

  • CH3-CH|-CH2-CH3

  • CH3-CH2-CH2-CH2-

  • CH3-C(C2H6)-


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