Advertisements
Advertisements
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)
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.
APPEARS IN
संबंधित प्रश्न
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.
Give reasons:
The dipole moment of chlorobenzene is lower than that of cyclohexyl chloride.
Write the product formed on reaction of D-glucose with Br2 water.
What is Grignard reagent?
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?