हिंदी

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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प्रश्न

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

विकल्प

  • I < II < III < IV

  • II < I < III < IV

  • III < IV < II < I

  • IV < III < I < II

  • I < II < IV < III

MCQ
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उत्तर

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
  क्या इस प्रश्न या उत्तर में कोई त्रुटि है?
अध्याय 10: Halogen Derivatives - Exercises [पृष्ठ २३१]

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बालभारती Chemistry [English] Standard 12 Maharashtra State Board
अध्याय 10 Halogen Derivatives
Exercises | Q 1. i. | पृष्ठ २३१

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\[\begin{array}{cc}
\ce{CH3-CH-C2H5}\\
|\\
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(III) 

(IV)

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\phantom{.....}|\\
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\phantom{.....}|\\
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\end{array}\]


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|\phantom{.....}\\
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\end{array}\]
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  benzyl halide
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\[\ce{CH3C(C2H5)2CH2Br}\]


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