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4-Aminophenol: spot the fabricated intermediate

Single question

Two-step route to 4-aminophenol: reduce nitrobenzene to phenylhydroxylamine, then run the Bamberger rearrangement in dilute H2SO4. Step 2 draws an isolated intermediate. Inspect that structure carefully.

Bamberger rearrangement of phenylhydroxylamine
Nitrenium ion intermediates
Distinguishing fused-ring inventions from real cationic intermediates

Find the flaw

Click the step that contains the flaw, or pick “No flaw” if you think every step is correct.