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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?
Chlorobenzene is extremely less reactive towards a nucleophilic substitution reaction. Give two reasons for the same.
The presence of nitro group (−NO2) at o/p positions increases the reactivity of haloarenes towards nucleophilic substitution reactions.
How the following conversion can be carried out?
Chlorobenzene to p-nitrophenol
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.
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) |  |
Allyl chloride is hydrolysed more readily than n-propyl chloride. Why?
Assertion: Chlorobenzene is resistant to nucleophilic substitution reaction at room temperature.
Reason (R): C–Cl bond gets weaker due, to resonance.
In the reaction, \[\mathrm{CH}_3\mathrm{C}\equiv\mathrm{\overline{C}Na}^++(\mathrm{CH}_3)_2\mathrm{CHCl}\to\] the product formed is ______.
