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The correct order of increasing reactivity of C-X bond towards nucleophile in the following compounds is: (I) (II) (III) (CH3)3 C-X (IV) (CH3)2 CH-X - Chemistry

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Question

The correct order of increasing reactivity of C-X bond towards nucleophile in the following compounds is:

(I)

(II)

(III) (CH3)3 C-X

(IV) (CH3)2 CH-X

Options

  • I < II < III < IV

  • II < I < III < IV

  • III < IV < II < I

  • IV < III < I < II

  • I < II < IV < III

MCQ

Solution

I < II < IV < III

Explanation:

Alkyl halides are more reactive than aryl halides. This is because of the partial double bond character between the benzene ring and the halogen. Further, in alkyl halides, the greater the stability of carbocation formed, the more would be the reactivity. Thus, the tertiary halide is more reactive. Nitro group which is electron-withdrawing increases the reactivity of aryl halide.

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Notes

The correct option is not given in the textbook.

Classification of Halogen Derivatives
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Chapter 10: Halogen Derivatives - Exercises [Page 231]

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Balbharati Chemistry [English] 12 Standard HSC
Chapter 10 Halogen Derivatives
Exercises | Q 1. i. | Page 231

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