Advertisements
Advertisements
Question
Chlorobenzene is extremely less reactive towards a nucleophilic substitution reaction. Give two reasons for the same.
Advertisements
Solution
Chlorobenzene is extremely less reactive towards a nucleophilic substitution reaction because of the following reasons:
(1) Resonance effect: The electron pair on chlorine atom is in conjugation with the π - electrons of the benzene ring which results in the following resonance structures:

-
This results in delocalization of the electrons of C − Cl bond and a partial double bond character develops in the bond, which makes it difficult for the nucleophile to cleave the C − Cl bond.
(2) The nucleophile suffers repulsion from the increased electron density on the benzene ring as a result the nucleophile is unable to make a close approach for the attack on the molecule.
APPEARS IN
RELATED QUESTIONS
What happens when \[\ce{CH3 - Br}\] is treated with KCN?
Write the final product(s) in each of the following reactions:

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
Out of (CH3)3 C-Br and (CH3)3 C-I, which one is more reactive towards SN1 and why?
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) | ![]() |
Haloarenes are less reactive than haloalkanes and haloalkenes. Explain.
Assertion: Chlorobenzene is resistant to nucleophilic substitution reaction at room temperature.
Reason (R): C–Cl bond gets weaker due, to resonance.






