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  2. Carbon–carbon bond - Wikipedia

    en.wikipedia.org/wiki/Carboncarbon_bond

    In fact, the carbon atoms in the single bond need not be of the same hybridization. Carbon atoms can also form double bonds in compounds called alkenes or triple bonds in compounds called alkynes. A double bond is formed with an sp 2-hybridized orbital and a p-orbital that is not involved in the hybridization. A triple bond is formed with an sp ...

  3. Orbital hybridisation - Wikipedia

    en.wikipedia.org/wiki/Orbital_hybridisation

    For this molecule, carbon sp 2 hybridises, because one π (pi) bond is required for the double bond between the carbons and only three σ bonds are formed per carbon atom. In sp 2 hybridisation the 2s orbital is mixed with only two of the three available 2p orbitals, usually denoted 2p x and 2p y. The third 2p orbital (2p z) remains unhybridised.

  4. Double bond rule - Wikipedia

    en.wikipedia.org/wiki/Double_bond_rule

    In chemistry, the double bond rule states that elements with a principal quantum number (n) greater than 2 for their valence electrons (period 3 elements and higher) tend not to form multiple bonds (e.g. double bonds and triple bonds).

  5. Double bond - Wikipedia

    en.wikipedia.org/wiki/Double_bond

    In chemistry, a double bond 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 ...

  6. Carbon–oxygen bond - Wikipedia

    en.wikipedia.org/wiki/Carbonoxygen_bond

    A carbonoxygen bond is a polar covalent bond between atoms of carbon and oxygen. [ 1 ] [ 2 ] [ 3 ] : 16–22 Carbonoxygen bonds are found in many inorganic compounds such as carbon oxides and oxohalides , carbonates and metal carbonyls , [ 4 ] and in organic compounds such as alcohols , ethers , and carbonyl compounds .

  7. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    In diboron the 1s and 2s electrons do not participate in bonding but the single electrons in the 2p orbitals occupy the 2πp y and the 2πp x MO's resulting in bond order 1. Because the electrons have equal energy (they are degenerate) diboron is a diradical and since the spins are parallel the molecule is paramagnetic. MO diagram of diboron ...

  8. Carbonyl group - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_group

    In organic chemistry, a carbonyl group is a functional group with the formula C=O, composed of a carbon atom double-bonded to an oxygen atom, and it is divalent at the C atom. It is common to several classes of organic compounds (such as aldehydes, ketones and carboxylic acid), as part of many larger functional groups. A compound containing a ...

  9. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    For a tetrahedral molecule such as difluoromethane with two types of atom bonded to the central atom, the C-F bond to the more electronegative substituent (F) will involve a carbon orbital with less s character than the C-H bond, so that the angle between the C-F bonds is less than the tetrahedral bond angle of 109.5°. [15] [23]