What is the slow step in electrophilic aromatic substitution?
Nucleophilic Aromatic Substitution

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Chemistry, Science
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11th Grade - University
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Hard
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Formation of the carbocation intermediate
Restoration of aromaticity
Attack of the nucleophile
Formation of the leaving group
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
In nucleophilic aromatic substitution, what type of charge is present on the intermediates?
Double charge
Neutral charge
Negative charge
Positive charge
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What effect do electron-withdrawing groups have on the intermediate in nucleophilic aromatic substitution?
Convert the intermediate to a different compound
Stabilize the intermediate
Have no effect
Destabilize the intermediate
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is a Meisenheimer adduct?
An intermediate in nucleophilic aromatic substitution
A product of SN2 reaction
A catalyst in aromatic reactions
A type of electrophile
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which halogen is considered the best leaving group in nucleophilic aromatic substitution?
Fluorine
Iodine
Chlorine
Bromine
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the role of fluorine in nucleophilic aromatic substitution?
It increases the reaction temperature
It stabilizes the nucleophile
It acts as a catalyst
It polarizes the carbon-halogen bond
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is a benzyne?
A catalyst in substitution reactions
A type of nucleophile
An intermediate with a triple bond
A stable aromatic compound
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