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प्रश्न
Write chemical equation in support of your answer.
Out of 
Cl and 
CH2- Cl, which one is more reactive towards nucleophilic substitution reaction and why?
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उत्तर
CH2 - Cl , will be more reactive towards SN2 reaction as in case of reaction as in case of Cl the back side attack will be very difficult.
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संबंधित प्रश्न
What happens when \[\ce{CH3 - Br}\] is treated with KCN?
The presence of nitro group (−NO2) at o/p positions increases the reactivity of haloarenes towards nucleophilic substitution reactions.
Give reasons:
The dipole moment of chlorobenzene is lower than that of cyclohexyl chloride.
Assertion: Presence of a nitro group at ortho or para position increases the reactivity of haloarenes towards nucleophilic substitution.
Reason: Nitro group, being an electron-withdrawing group decreases the electron density over the benzene ring.
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) \[\begin{array}{cc}
\phantom{....}\ce{CH3 - CH - CH2Br}\\
\phantom{}|\\
\phantom{....}\ce{C2H5}\phantom{}
\end{array}\]
Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.
| (a) |  |
| (b) |  |
| (c) |  |
Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.
| (a) |  |
| (b) |  |
| (c) |  |
Haloarenes are less reactive than haloalkanes and haloalkenes. Explain.
Why haloarenes are not reactive towards nucleophilic substitution reaction? Give two reactions.
Identify the final product [D] obtained in the following sequence of reactions.
\[\ce{CH3CHO \underset{ii) H2O+}{\overset{i) LiAlH4}{->}} [A] \underset{\triangle}{\overset{H2SO4}{->}} [B]}\]
