(Solved): 2. Pyrrole is highly activated towards EAS reactions compared to a regular benzene ring. Please just ...

2. Pyrrole is highly activated towards EAS reactions compared to a regular benzene ring. Please justify this. "Hint: What is a common structural feature among activating groups, why do they make aromatic rings more nucleophilic, and what does pyrrole have in common with these?* 3. a. Please write a mechanism to account for the formation of the product shown in the EAS reaction below. Please also make sure that after you attack with a pi bond, you draw all resonance structures for the resulting cation. "Note: \( \mathrm{E}+ \) represents a general electrophile. You can use "B" to represent a generic base. b. Please write a mechanism to account for the formation of the product shown in the EAS reaction below. Please also make sure that after you attack with a pi bond, you draw all resonance structures for the resulting cation. *Note: \( \mathrm{E}+ \) represents a general electrophile. You can use "B" to represent a generic base. c. Given your answers above, which product do you predict will be the major product? You can just d. Justify your answer to \( \mathrm{c} \). Why did you predict that this would be the major product? It may help to look back at your answers to \( a \). and \( b \).