Multiple Choice
What is the driving force for losing a proton as the last step in electrophilic aromatic substitution?
A) To neutralize the base that is present
B) To make room for the electrophile
C) To make the ring more reactive
D) To rearomatize the ring system
Correct Answer:
Verified
Correct Answer:
Verified
Q1: What is the major product of electrophilic
Q2: How can polyalkylation be minimized in Friedel-Crafts
Q3: Rank the following activating groups in order
Q5: What is a major problem with Friedel-Crafts
Q6: What is (are)the product(s)of the following reaction?
Q7: What is the best choice of reagent
Q8: What reagents would be necessary to produce
Q9: Which of the following substituents are deactivators
Q10: What are the two effects that have
Q11: What are the product(s)of the following reaction?