A double bond in chemistry is a chemical bond between two chemical elements involving four bonding electrons instead of the usual two. The most common double bond, that between two carbon atoms, can be found in alkenes. Many types of double bonds between two different elements exist, for example in a carbonyl group with a carbon atom and an oxygen atom. Other common double bonds are found in azo compounds (N=N), imines (C=N) and sulfoxides (S=O). In skeletal formula the double bond is drawn as two parallel lines (=) between the two connected atoms; typographically, the equals sign is used for this.^[1][2]

Double bonds are stronger than single bonds and double bonds are also shorter. The bond order is two. Double bonds are also electron-rich, which makes them reactive.

ethylene	acetone	dimethyl sulfoxide
Common chemical compounds with double bonds

The type of bonding can be explained in terms of orbital hybridization. In ethylene each carbon atom has three sp² orbitals and one p-orbital. The three sp² orbitals lie in a plane with 120° angles. The p-orbital is perpendicular to this plane. When the carbon atoms approach each other, two of the sp² orbitals overlap to form a sigma bond. At the same time, the two p-orbitals approach (again in the same plane) and together they form a pi-bond. For maximum overlap, the p-orbitals have to remain parallel, and, therefore, rotation around the central bond is not possible. This property gives rise to cis-trans isomerism. Double bonds are shorter than single bonds because p-orbital overlap is maximized.

2 sp2 orbitals (total of 3 such orbitals) approach to form a sp2-sp2 sigma bond		Two p-orbitals overlap to form a pi-bond in a plane parallel to the sigma plane

With 133 pm, the C=C bond length is shorter than the C−C length in ethane with 154 pm. The double bond is also stronger, 636 (KJ/mol) versus 368 kJ/mole but not twice as much as the pi-bond is weaker than the sigma bond due to less effective pi-overlap.

In an alternative representation, the double bond results from two overlapping sp³ orbitals as in a bent bond.^[3]

In molecules with alternating double bonds and single bonds, p-orbital overlap can exist over multiple atoms in a chain, giving rise to a conjugated system. Conjugation can be found in systems such as dienes and enones. In cyclic molecules, conjugation can lead to aromaticity. In cumulenes two double bonds are adjacent.

Double bonds are common for period 2 elements carbon, nitrogen, and oxygen, and less common with elements of higher periods. Metals, too, can engage in multiple bonding in a metal ligand multiple bond.

• doi:10.1002/chem.200401299

v t e Chemical bonds
Intramolecular (strong)	Covalent Electron deficiency 3c–2e 4c–2e 8c–2e Hypervalence 3c–4e Agostic Bent Coordinate (dipolar) Pi backbond Metal–ligand multiple bond Charge-shift Hapticity Conjugation Hyperconjugation Aromaticity homo bicyclo Metallic Metal aromaticity Ionic
Intermolecular (weak)	Van der Waals forces London dispersion Hydrogen Low-barrier Resonance-assisted Symmetric Dihydrogen bonds C–H···O interaction Noncovalent other Mechanical Halogen Chalcogen Metallophilic (aurophilic) Intercalation Stacking Cation–pi Anion–pi Salt bridge
Bond cleavage	Heterolysis Homolysis
Electron counting rules	Aromaticity Hückel's rule Baird's rule Möbius spherical Polyhedral skeletal electron pair theory Jemmis mno rules