Nitrobenzene · C₆H₅NO₂

C₆H₅NO₂ Lewis Structure

The nitro group requires N⁺/O⁻ formal charges in each contributor, with the N=O bond alternating between oxygens.

C₆H₅NO₂
C₆H₅—N⁺(=O)—O⁻
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

  1. Count 46 valence electrons. Include charge adjustments before drawing.
  2. Use the reviewed connectivity C₆H₅—N⁺(=O)—O⁻. Do not infer a different isomer from the formula alone.
  3. Place the required single, double or multiple bonds. Keep a running electron total.
  4. 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.
  5. 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.

Common mistakes

  • Using 42 instead of 46 valence electrons
  • Drawing neutral nitrogen with five bonds
  • Omitting the second nitro resonance contributor

Last reviewed: 2026-07-16. Educational reference only; verify graded work with course materials.