Isobutane (2-Methylpropane) · i-C₄H₁₀

i-C₄H₁₀ Lewis Structure

The branched carbon skeleton distinguishes isobutane from n-butane even though both have formula C₄H₁₀.

i-C₄H₁₀
(CH₃)₃CH
Reviewed stored connectivity; detailed electron placement is explained below
Total valence electrons26
Reviewed connectivity(CH₃)₃CH
GeometryTetrahedral at each carbon
Support levelReviewed guide

Isobutane (2-Methylpropane) overview

The stored Lewis connectivity is (CH₃)₃CH. The branched carbon skeleton distinguishes isobutane from n-butane even though both have formula C₄H₁₀.

How to draw i-C₄H₁₀

  1. Count 26 valence electrons. Include charge adjustments before drawing.
  2. Use the reviewed connectivity (CH₃)₃CH. 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 branched carbon skeleton distinguishes isobutane from n-butane even though both have formula C₄H₁₀.
  5. Verify the total electron count and geometry. The reviewed geometry is Tetrahedral at each carbon.

Why this example matters

The branched carbon skeleton distinguishes isobutane from n-butane even though both have formula C₄H₁₀.

Scope and model limits

The separate record prevents the name isobutane from resolving to the n-butane connectivity.

Common mistakes

  • Using the straight-chain skeleton
  • Adding a C=C bond
  • Treating constitutional isomers as resonance forms

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