Content protected from screenshots
GKFix.in
General Knowledge
Categories
Concept Builder Quiz
About Us
Start Quiz
Home
My Profile
General Knowledge
Categories
Concept Builder
Start Quiz
Logout
GKFix MCQ Question
Test your knowledge and learn something new
Home
ORGANIC COMPOUNDS CONTAINING HALOGENS
Question #49838
Back to Home
View All ORGANIC COMPOUNDS CONTAINING HALOGENS Questions
64 Views
Question
Why don't methyl halides (CH3X) typically undergo SN1 reactions?
A. They are too sterically hindered
B. The C-X bond is too strong
C. The methyl carbocation (CH3+) is highly unstable
D. They cannot form a carbocation
Check Answer
Share on Twitter
Share on Facebook
Copy Link
Related Questions
What is the major product when 1-bromobutane reacts with a strong nucleophile like NaOH?
61
Why is the SN2 reaction described as a concerted process?
57
What is the expected stereochemical outcome when an SN1 reaction occurs on an optically active alkyl...
37