Home
Class 12
CHEMISTRY
The leaving group ability of halide ions...

The leaving group ability of halide ions for `S_(N)2` reaction is

A

`Cl^(-)gtF^(-)gtBr^(-)gtl^(-)`

B

`l^(-)gtBr^(-)gtCl^(-)gtF^(-)`

C

`Cl^(-)gtF^(-)gtl^(-)gtBr^(-)`

D

`Br^(-)gtl^(-)gtF^(-)gtCl^(-)`

Text Solution

Verified by Experts

The correct Answer is:
D
Promotional Banner

Topper's Solved these Questions

  • HALOALKANES (ALKYL HALIDE)

    ARIHANT PUBLICATION|Exercise PART-II- QUESTIONS FOR ASSESSMENT (VERY SHORT ANSWER TYPE QUESTIONS) |5 Videos
  • HALOALKANES (ALKYL HALIDE)

    ARIHANT PUBLICATION|Exercise PART-II- QUESTIONS FOR ASSESSMENT (SHORT ANSWER TYPE I QUESTIONS) |7 Videos
  • HALOALKANES (ALKYL HALIDE)

    ARIHANT PUBLICATION|Exercise PART-II- QUESTION FOR PRACTICE (LONG ANSWER TYPE II QUESTIONS)|12 Videos
  • GROUP 18 ELEMENTS NOBLEGASES

    ARIHANT PUBLICATION|Exercise CHAPTER PRACTICE ( Long Answer Type Questions )|6 Videos
  • PHENOLS

    ARIHANT PUBLICATION|Exercise CHAPTER PRACTICE (Long Answer Type Questions )|1 Videos

Similar Questions

Explore conceptually related problems

Discuss S_N 2 reaction.

The order of reactivities of the following alkyl halides for a S_N^2 reactions is:

Write a note on S_N1 reaction.

Which compound in each of the following pairs will react faster in S_(N)2 reaction with OH^(-) and why? CH_(3)Br or CH_(3)I

Which compound in each of the following pairs will react faster in S_(N)2 reaction with OH^(-) and why? (CH_(3))_(3)C ClorCH_(3)Cl

Which of the following alkyl halide undergoes faster SN^(1) reaction?