Home
Class 12
CHEMISTRY
Bacause of the resonance stabilization...

Bacause of the resonance stabilization of Arylhalides they are unreactive toward normal nuclephilic substitution reactions . However arylhalides having strong electron withdrawing groups at ortho and para positions give aromatic nucleophilic substitution reactions `(S_(N)Ar` mechanism ) , which involves a resonance stablilized carbanion called Meisenheimer complex

What would be the product of the given reaction ?

A

B

C

D

Text Solution

Verified by Experts

The correct Answer is:
B
Promotional Banner

Topper's Solved these Questions

  • HALOALKANES AND HALOARENES

    AAKASH INSTITUTE ENGLISH|Exercise Assignment (Section - E) ( Assertion - Reason type Questions )|7 Videos

  • HALOALKANES AND HALOARENES

    AAKASH INSTITUTE ENGLISH|Exercise Assignment (Section - F) (Matrix - Match Type Question )|4 Videos

  • HALOALKANES AND HALOARENES

    AAKASH INSTITUTE ENGLISH|Exercise Assignment (Section - C ) ( Objective Type Question(More than one options are correct ))|17 Videos

  • GENERAL PRINCIPLES AND PROCESSES OF ISOLATION OF ELEMENTS

    AAKASH INSTITUTE ENGLISH|Exercise Try Yourself|33 Videos

  • HYDROCARBONS

    AAKASH INSTITUTE ENGLISH|Exercise Assignment(Section - C) (Previous Years Questions)|60 Videos

Similar Questions

Explore conceptually related problems

Bacause of the resonance stabilization of Arylhalides they are unreactive toward normal nuclephilic substitution reactions . However arylhalides having strong electron withdrawing groups at ortho and para positions give aromatic nucleophilic substitution reactions (S_(N)Ar mechanism ) , which involves a resonance stablilized carbanion called Meisenheimer complex Which of the following statement is // are true ?

Bacause of the resonance stabilization of Arylhalides they are unreactive toward normal nuclephilic substitution reactions . However arylhalides having strong electron withdrawing groups at ortho and para positions give aromatic nucleophilic substitution reactions (S_(N)Ar mechanism ) , which involves a resonance stablilized carbanion called Meisenheimer complex Which arylhalide is most reactive toward S_(N)Ar mechanism ?

Aryl halides are less reactive towards nucleophilic substitution reaction as compared to alkyl halides due to

Phenol is least reactive for aromatic nucleophilic substitution because

What are nucleophilic substitution reactions ? Give an example.

Anyl halides are practically inert toward nucleophilic substitution reactions . The reasons for this fact are

Which of the following is least reactive in a nucleophilic substitution reaction?

Although chlorine is an electron withdrawing group, yet it is ortho-, para- directing in electrophilic aromatic substitution reactions. Why?