shaalaa.com
S

Solution - Chemical Reactions of Haloalkanes and Haloarenes - Reactions of Haloalkanes - Nucleophilic Substitution Reactions

Account
User


Login
Register


      Forgot password?
Share
Notifications

View all notifications
Books Shortlist
Your shortlist is empty

Question

Which would undergo SN2 reaction faster in the following pair and why ?

Solution

You need to to view the solution
Is there an error in this question or solution?

Similar questions

 Give reasons for the following:

(CH3)3C–O–CH3 on reaction with HI gives (CH3)3C–I and CH3–OH as the main products and not (CH3)3C–OH and CH3–I.

view solution

Arrange the compounds of each set in order of reactivity towards SN2 displacement:

1-Bromo-3-methylbutane, 2-Bromo-2-methylbutane, 3-Bromo-2- methylbutane

view solution

Arrange the compounds of each set in order of reactivity towards SN2 displacement:

1-Bromobutane, 1-Bromo-2,2-dimethylpropane, 1-Bromo-2-methylbutane, 1-Bromo-3-methylbutane.

view solution

C–Cl bond length in chlorobenzene is shorter than C–Cl bond length in CH3–Cl.

view solution

Predict all the alkenes that would be formed by dehydrohalogenation of the following halides with sodium ethoxide in ethanol and identify the major alkene:

1-Bromo-1-methylcyclohexane

view solution

Reference Material

S