Skip to main content
Organic Chemistry
My Course
Learn
Exam Prep
AI Tutor
Study Guides
Textbook Solutions
Flashcards
Explore
Try the app
My Course
Learn
Exam Prep
AI Tutor
Study Guides
Textbook Solutions
Flashcards
Explore
Try the app
Back
27. Heterocycles - Part 1 of 2!
Download worksheet
Problem 1
Problem 2
Problem 3
Problem 4
Problem 5
Problem 6
Problem 7
Problem 8
Problem 9
Problem 10
Problem 11
Problem 12
27. Heterocycles - Part 1 of 2!
Download worksheet
Practice
Summary
Previous
8 of 12
Next
27. Heterocycles / Reactions of Pyrrole, Furan, and Thiophene / Problem 8
Problem 8
During electrophilic aromatic substitution, why is substitution at the 2 position favored over the 3 position in pyrrole?
A
Substitution at carbon 2 allows for more resonance stabilization.
B
Carbon 3 is less accessible to electrophiles.
C
Substitution at carbon 2 prevents loss of electron density.
D
Substitution at carbon 3 disrupts aromaticity more significantly.
AI tutor
0
0 Comments
Show Answer
More options