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
HYDROCARBONS
Question #47280
Back to Home
View All HYDROCARBONS Questions
31 Views
Question
Which of the following best explains why the -CH₃ group is ortho and para directing?
A. Due to hyperconjugation and weak +I (inductive donation) effects, increasing electron density at ortho/para positions.
B. Because the -CH₃ group is very large and sterically blocks the meta position.
C. Because the -CH₃ group is strongly electron-withdrawing.
D. Because the -CH₃ group forms strong hydrogen bonds.
Check Answer
Share on Twitter
Share on Facebook
Copy Link
Related Questions
What is the key difference between chain isomers and position isomers?
27
What is the molecular formula of the product formed when cyclohexene reacts with hot, acidic KMnO4?
11
Arrange toluene, p-H3C–C6H4–NO2, and p-O2N–C6H4–NO2 in order of decreasing reactivity with a...
15