Double bond


A double bond in chemistry is a covalent bond between two atoms involving four bonding electrons as opposed to two in a single bond. Double bonds occur most commonly between two carbon atoms, for example in alkenes. Many double bonds exist between two different elements: for example, in a carbonyl group between a carbon atom and an oxygen atom. Other common double bonds are found in azo compounds, imines and sulfoxides. In a skeletal formula, a double bond is drawn as two parallel lines between the two connected atoms; typographically, the equals sign is used for this. Double bonds were first introduced in chemical notation by Russian chemist Alexander Butlerov.
Double bonds involving carbon are stronger than single bonds and are also shorter. The bond order is two. Double bonds are also electron-rich, which makes them potentially more reactive in the presence of a strong electron acceptor.
Chemical compounds with double bonds
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Ethylene
Carbon-carbon
double bond
Acetone
Carbon-oxygen
double bond
Dimethyl sulfoxide
Sulfur-oxygen
double bond
Diazene
Nitrogen-nitrogen
double bond

Double bonds in alkenes

The type of bonding can be explained in terms of orbital hybridisation. 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 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 approach to form a sp2-sp2 sigma bondTwo p-orbitals overlap to form a pi-bond in a plane parallel to the sigma planepi bond in ethylene

With 133 pm, the ethylene 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−1 versus 368 kJ mol−1 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.

Types of double bonds between atoms

Variations

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.

Group 14 alkene homologs

Double bonded compounds, alkene homologs, R2E=ER2 are now known for all of the heavier group 14 elements. Unlike the alkenes these compounds are not planar but adopt twisted and/or trans bent structures. These effects become more pronounced for the heavier elements. The distannene 2CHSn=SnCH2 has a tin-tin bond length just a little shorter than a single bond, a trans bent structure with pyramidal coordination at each tin atom, and readily dissociates in solution to form 2CHSn:. The bonding comprises two weak donor acceptor bonds, the lone pair on each tin atom overlapping with the empty p orbital on the other. In contrast, in disilenes each silicon atom has planar coordination but the substituents are twisted so that the molecule as a whole is not planar. In diplumbenes the Pb=Pb bond length can be longer than that of many corresponding single bonds Plumbenes and stannenes generally dissociate in solution into monomers with bond enthalpies that are just a fraction of the corresponding single bonds. Some double bonds plumbenes and stannenes are similar in strength to hydrogen bonds. The Carter-Goddard-Malrieu-Trinquier model can be used to predict the nature of the bonding.