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प्रश्न
Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.
| (a) |  |
| (b) |  |
| (c) |  |
पर्याय
(a) < (b) < (c)
(b) < (a) < (c)
(c) < (b) < (a)
(a) < (c) < (b)
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उत्तर
(c) < (b) < (a)
Explanation:
The presence of electron releasing group at ortho- and para-positions decreases the reactivity of haloarenes. Because of the possible repulsion, it is less likely for the electron-rich nucleophile to approach electron-rich arenes. The more the electron-releasing group is attached lesser, will be the rate of reaction.
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संबंधित प्रश्न
What happens when \[\ce{CH3 - Br}\] is treated with KCN?
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Write chemical equation in support of your answer.
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Cl and 
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Which of the following compounds will give racemic mixture on nucleophilic substitution by \[\ce{OH-}\] ion?
(a) \[\begin{array}{cc}
\phantom{}\ce{CH3 - CH - Br}\\
\phantom{}|\\
\phantom{....}\ce{C2H5}\phantom{}
\end{array}\]
(b) \[\begin{array}{cc}
\phantom{..}\ce{Br}\\
\phantom{}|\\
\phantom{}\ce{CH3 - C - CH3}\\
\phantom{}|\\
\phantom{....}\ce{C2H5}\phantom{}
\end{array}\]
(c) \[\begin{array}{cc}
\phantom{....}\ce{CH3 - CH - CH2Br}\\
\phantom{}|\\
\phantom{....}\ce{C2H5}\phantom{}
\end{array}\]
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| (a) |  |
| (b) |  |
| (c) |  |
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| (a) |  |
| (b) |  |
| (c) |  |
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| (a) |  |
| (b) |  |
| (c) |  |
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