Reviewed stored connectivity; detailed electron placement is explained below
Total valence electrons46
Reviewed connectivityC₆H₅—N⁺(=O)—O⁻
GeometryPlanar or nearly planar conjugated nitro group
Support levelReviewed guide
Nitrobenzene overview
The stored Lewis connectivity is C₆H₅—N⁺(=O)—O⁻. The nitro group requires N⁺/O⁻ formal charges in each contributor, with the N=O bond alternating between oxygens.
How to draw C₆H₅NO₂
Count 46 valence electrons. Include charge adjustments before drawing.
Use the reviewed connectivity C₆H₅—N⁺(=O)—O⁻. Do not infer a different isomer from the formula alone.
Place the required single, double or multiple bonds. Keep a running electron total.
Complete terminal valence shells and add lone pairs or formal charges. The nitro group requires N⁺/O⁻ formal charges in each contributor, with the N=O bond alternating between oxygens.
Verify the total electron count and geometry. The reviewed geometry is Planar or nearly planar conjugated nitro group.
Why this example matters
The nitro group requires N⁺/O⁻ formal charges in each contributor, with the N=O bond alternating between oxygens.
Scope and model limits
The aromatic ring and nitro group both involve delocalization. One Lewis contributor cannot represent the complete electron distribution.