The Azide ion Lewis structure is N–N double bond and N–N double bond; the central N has 2 electron domains (0 lone pairs), giving a linear electron-domain arrangement and a linear molecular geometry with a 180° bond angle. N is best described as sp-hybridized, and Azide ion is nonpolar because the bond dipoles cancel by molecular symmetry.
Figure 1: Lewis Structure of Azide ion (N3-)
| Chemical Formula | N3- |
| CAS Number | 14343-69-2 |
| Net Charge | -1 |
| Total Valence Electrons | 16 |
| Lewis Structure | N–N double bond and N–N double bond |
| Electron-Domain Geometry | linear |
| Molecular Geometry | linear |
| Hybridization Model | sp (central N) |
| Bond Angle | 180° |
| Polarity | Nonpolar molecule |
In aqueous and process chemistry, N3- exists as the anion Azide ion ion. It is encountered as a counterion and a controlled source of N in salts, buffers, electrochemistry and analytical protocols, and as a reactant in syntheses that require a defined equivalent of N-containing material.
To draw the Azide ion Lewis structure we first count the total valence electrons. N3- contains 3×5 (N) − 1 (net anion); the net charge of -1 gives a total of 16 valence electrons to place.
The central atom is N. It is the least electronegative atom capable of forming multiple bonds and is surrounded by the more electronegative terminal atom(s); hydrogen, when present, always occupies a terminal position. Electronegativity considerations place the electron density toward the terminal atom(s).
Total valence electrons = 3×5 (N) − 1 (net anion) = 16 electrons.
Place N at the center and connect each surrounding atom with a single bond, complete octets on the terminal atoms, and place any remaining electrons on the central atom. The resulting electron distribution is: N–N double bond and N–N double bond; no lone pairs on N.
Counting bonding and nonbonding electrons around N therefore satisfies the octet/expanded-octet requirement for the drawn structure.
This species is best represented by resonance structures; the π bonding is delocalized over the equivalent terminal atom(s), so all N–terminals bonds are equivalent in the resonance hybrid.
VSEPR theory states that the 2 electron domains around N arrange to minimize mutual repulsion, giving an linear electron-domain geometry.
Because 0 of these domains are lone pair(s) — and lone pairs repel more strongly than bonding pairs — the observed molecular geometry is linear; the N bond angle is set to 180° rather than the ideal value for the electron-domain geometry.
A useful VSEPR approximation is: lone pair–lone pair repulsion > lone pair–bonding pair repulsion > bonding pair–bonding pair repulsion. With 0 lone pair(s) on N, the lone-pair domains occupy positions that minimize overall repulsion while pushing the bonding domains (and therefore the bonded atoms) closer together.
In the conventional localized-bond model, N uses sp hybrid orbitals to form the 2 equivalent electron-domain directions (2 bonding + 0 lone pair).
Formal charge on central N = V − N − ½B = 5 − 0 − ½×8 = 1. The nonzero formal charge is distributed by resonance / charge separation; the drawn structure is the lowest-energy contributor.
Azide ion is nonpolar. Although individual N–terminal bonds are polar when the atoms differ in electronegativity, the linear geometry makes their vector sum zero, so there is no net molecular dipole.
A common misconception is that polar bonds guarantee a polar molecule. Azide ion shows the opposite: identical bond dipoles arranged with linear symmetry cancel exactly, yielding a nonpolar species.
Interpretation consistent with standard VSEPR / molecular-geometry references.Its nonpolar character governs solvation and intermolecular behavior; specify grade and handling when sourcing.
| Species | Formula | Central Atom | Electron Domains | Molecular Geometry | Polarity |
|---|---|---|---|---|---|
| Azide ion | N3- | N | 2 | linear | Nonpolar |
| Ammonia | H3N | N | 4 | trigonal pyramidal | Polar |
| Ammonium | H4N | N | 4 | tetrahedral | Nonpolar |
| Hydrazine | H4N2 | N | 4 | trigonal pyramidal | Polar |
| Nitrogen | N2 | N | 2 | linear (diatomic) | Nonpolar |
| Nitric oxide | NO | N | 3 | linear (diatomic) | Polar |
Azide ion is nonpolar. Its linear symmetry cancels the bond dipoles exactly.
N–N double bond and N–N double bond; no lone pairs on N. It uses all 16 valence electrons and the preferred structure carries a formal charge of 1 on the central atom.
The N angle is about 180°. Lone-pair repulsion compresses the angle from the ideal linear value.
The conventional model is sp. Azide ion has 2 electron domains around the central N.
The CAS number is 14343-69-2. PubChem (CID 33558) and NIST identify this with N3-; use it to locate suppliers and database records.
Technical scope: Lewis structures, VSEPR and hybridization are model-based descriptions for chemical communication and structure prediction; actual molecular electronic structure is more accurately represented by molecular-orbital and quantum-chemical methods. Commercial grades vary substantially by supplier and intended use; CAS 14343-69-2 identifies the substance, not a universal purity specification.
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