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प्रश्न
In the following pair of halogen compounds, which compound undergoes a faster SN1 reaction?

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उत्तर
The activity of halogen compounds in SN1 reaction depends on the stability of the carbocation formed due to ionization. The order of stability is tertiary > secondary > primary. Hence, 2° alkyl chloride is more active than 1° alkyl chloride. Hence, 2° alkyl chloride is more active in SN1 reaction.
reacts faster due to the greater stability of 2° carbocation than 1° carbocation.
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संबंधित प्रश्न
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\[\begin{array}{cc}
\ce{CH3}\phantom{..}\\
|\phantom{....}\\
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\end{array}\]
(iv)
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\phantom{..}\ce{H}\\
\phantom{..}|\\
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\phantom{..}|\\
\phantom{.....}\ce{C2H5}
\end{array}\]
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| Column I | Column II | |
| (i) | ![]() |
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| (ii) | \[\begin{array}{cc} \ce{CH3 - CH = CH2 + HBr -> CH3 - CH - CH3}\\ \phantom{............................}|\phantom{}\\ \phantom{.............................}\ce{Br}\phantom{} \end{array}\] |
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| (iii) | ![]() |
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| (iv) | ![]() |
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