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  2. Carbon–nitrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbonnitrogen_bond

    Similar to carboncarbon bonds, these bonds can form stable double bonds, as in imines; and triple bonds, such as nitriles. Bond lengths range from 147.9 pm for simple amines to 147.5 pm for C-N= compounds such as nitromethane to 135.2 pm for partial double bonds in pyridine to 115.8 pm for triple bonds as in nitriles. [2]

  3. Imine - Wikipedia

    en.wikipedia.org/wiki/Imine

    In organic chemistry, an imine (/ ɪ ˈ m iː n / or / ˈ ɪ m ɪ n /) is a functional group or organic compound containing a carbonnitrogen double bond (C=N). The nitrogen atom can be attached to a hydrogen or an organic group (R). The carbon atom has two additional single bonds.

  4. 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 ...

  5. Ball-and-stick model - Wikipedia

    en.wikipedia.org/wiki/Ball-and-stick_model

    Double and triple bonds are usually represented by two or three curved rods, respectively, or alternately by correctly positioned sticks for the sigma and pi bonds. In a good model, the angles between the rods should be the same as the angles between the bonds , and the distances between the centers of the spheres should be proportional to the ...

  6. Bond length - Wikipedia

    en.wikipedia.org/wiki/Bond_length

    It is generally considered the average length for a carboncarbon single bond, but is also the largest bond length that exists for ordinary carbon covalent bonds. Since one atomic unit of length (i.e., a Bohr radius) is 52.9177 pm, the C–C bond length is 2.91 atomic units, or approximately three Bohr radii long.

  7. Double bond rule - Wikipedia

    en.wikipedia.org/wiki/Double_bond_rule

    Moreover, the multiple bonds of the elements with n=2 are much stronger than usual, because lone pair repulsion weakens their sigma bonding but not their pi bonding.) [2] An example is the rapid polymerization that occurs upon condensation of disulfur, the heavy analogue of O 2.

  8. Molecular model - Wikipedia

    en.wikipedia.org/wiki/Molecular_model

    This also allows double and triple bonds to be approximated by multiple single bonds. A modern plastic ball and stick model. The molecule shown is proline. The model shown to the left represents a ball-and-stick model of proline. The balls have colours: black represents carbon (C); red, oxygen (O); blue, nitrogen (N); and white, hydrogen (H).

  9. Diatomic molecule - Wikipedia

    en.wikipedia.org/wiki/Diatomic_molecule

    All diatomic molecules are linear and characterized by a single parameter which is the bond length or distance between the two atoms. Diatomic nitrogen has a triple bond, diatomic oxygen has a double bond, and diatomic hydrogen, fluorine, chlorine, iodine, and bromine all have single bonds. [6]