For the routine examples here, assign all bonding Electrons between different chemical elements to the more electronegative partner; divide bonding Electrons between identical chemical elements equally. Retain each lone pair on its original chemical atom. Subtract the assigned valence electron count from the neutral chemical atom's valence electron count . The IUPAC convention uses Allen electronegativity, based on free-chemical atom valence electron energies. Close electronegativity comparisons and some reversibly bound chemical compounds require care beyond this simple rule.[ref]
Figure 1. . Original bookkeeping diagrams, not electron density maps or measured partial atomic charges. Arrows indicate allocation of bonding Electrons; an equal split is used for O–O. The sodium hydride panel represents a formula unit of an ionic compound, not an isolated gas-phase molecule. Details.
The examples explain exceptions to memorized rules:
These drawings record allocations, not molecular geometry or a physical process of breaking the chemical bonds. In particular, the O–O line in the molecular oxygen panel only marks the connection; it does not assert a complete Lewis structure or spin state.

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