Answer:
The structure can be found on the attached documents
Explanation:
Answer:
3-methylthiophene > thiophene > benzene > 2-methylfuran
Explanation:
Primarily, five membered heterocyclic aromatic rings undergo nitration at carbon-2. This is because, nitration at carbon-2 leads to the formation of three resonance structures while attack at carbon-3 yields only two resonance structures, hence it is less stabilized.
The presence of a methyl group which donates electrons promotes the stabilization of the cation formed in the nitration of 3-methylthiophene.
2-methylfuran is the least reactive towards nitration because the 2-position has been blocked by a methyl group.
The answer is the choice A
Explanation:
1. c
2. b
3. b
4. d
5. c
6. b
7.c
8. c
9. d
10. c
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