Use app×
QUIZARD
QUIZARD
JEE MAIN 2026 Crash Course
NEET 2026 Crash Course
CLASS 12 FOUNDATION COURSE
CLASS 10 FOUNDATION COURSE
CLASS 9 FOUNDATION COURSE
CLASS 8 FOUNDATION COURSE
+1 vote
108 views
in Chemistry by (25.5k points)
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
image
Which of the following statement is `//` are true ?
A. `S_(N)Ar` proceeds through elimination `//` addition mechanism
B. Formation of elimination product is the rate determing step
C. Formation of Meisenheimer complex is the rate determining step
D. `S_(N)Ar` mechanism involves inversion of configuration

Please log in or register to answer this question.

Welcome to Sarthaks eConnect: A unique platform where students can interact with teachers/experts/students to get solutions to their queries. Students (upto class 10+2) preparing for All Government Exams, CBSE Board Exam, ICSE Board Exam, State Board Exam, JEE (Mains+Advance) and NEET can ask questions from any subject and get quick answers by subject teachers/ experts/mentors/students.

Categories

...