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Question 14 of 40 · 2.5 pts
Which of the following correctly describes the mechanism of electrophilic aromatic substitution in the nitration of benzene? A) The electrophile NO₂⁺ attacks the π system, forming an arenium ion intermediate, followed by loss of H⁺ to restore aromaticity. B) The reaction proceeds via an SN2 mechanism at the ring carbon, with direct displacement of a hydrogen atom. C) The nitro group replaces a carbon in the ring via a radical mechanism initiated by UV light. D) Benzene undergoes addition across a double bond, forming a stable cyclohexane derivative.
Same question. Now watch it collapse.
Step through each part of the mechanism. This is exactly how our lessons are structured — not memorization, but understanding.
Step 1 of 4
Identify the Mechanism Type
EAS (Electrophilic Aromatic Substitution) is the key. Any time benzene reacts with a strong electrophile, this is your mechanism. The aromatic ring acts as the nucleophile.
Mechanism
Benzene + E⁺ → Arenium Ion → Product
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