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The correct order of reactivity in electrophilic substitution reaction of the following compounds is:


(a)B > C > A > D
(b)D > C > B > A
(c)A > B > C > D
(d)B > A > C > D

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Important Questions on Some Basic Principles of Organic Chemistry
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Given below are two statements :
Statement I : Hyperconjugation is a permanent effect.
Statement II : Hyperconjugation in ethyl cation involves the overlapping of bond with empty orbital of other carbon.
Choose the correct option:

EASY
The most acidic proton and the strongest nucleophilic nitrogen in the following compound
respectively, are

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(i)
(ii)
(iii)
(iv)

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EASY

HARD
The correct order of the stability of the following compounds based on hyperconjugation is

EASY


HARD
Increasing order of stability of the resonance structure is:

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Among the given species the Resonance stabilised carbocations are:

EASY

HARD
Number of electrophillic centres in the given compound is___

EASY

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EASY

Hyperconjugation occurs in:

