English
Karnataka Board PUCPUC Science 2nd PUC Class 12

Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.

Advertisements
Advertisements

Question

Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.

(a)
(b)
(c)

Options

  • (a) < (b) < (c)

  • (c) < (b) < (a)

  • (a) < (c) < (b)

  • (c) < (a) < (b)

MCQ
Advertisements

Solution

(a) < (c) < (b)

Explanation:

The presence of an electron-withdrawing group (−NO2) at the ortho and para position facilitates nucleophilic substitution. The effect of the presence of the electron-withdrawing group is very less at the meta position.

shaalaa.com
  Is there an error in this question or solution?
Chapter 10: Haloalkanes and Haloarenes - Exercises [Page 139]

APPEARS IN

NCERT Exemplar Chemistry Exemplar [English] Class 12
Chapter 10 Haloalkanes and Haloarenes
Exercises | Q I. 26. | Page 139

RELATED QUESTIONS

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


Write the product formed on reaction of D-glucose with Br2 water.


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? 


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)

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.


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.


Why haloarenes are not reactive towards nucleophilic substitution reaction? Give two reactions.


In the reaction, \[\mathrm{CH}_3\mathrm{C}\equiv\mathrm{\overline{C}Na}^++(\mathrm{CH}_3)_2\mathrm{CHCl}\to\] the product formed is ______.


Identify the final product [D] obtained in the following sequence of reactions.

\[\ce{CH3CHO \underset{ii) H2O+}{\overset{i) LiAlH4}{->}} [A] \underset{\triangle}{\overset{H2SO4}{->}} [B]}\]


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×