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  2. Carbon–nitrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbonnitrogen_bond

    A carbonnitrogen bond is a covalent bond between carbon and nitrogen and is one of the most abundant bonds in organic chemistry and biochemistry. [ 1 ] Nitrogen has five valence electrons and in simple amines it is trivalent , with the two remaining electrons forming a lone pair .

  3. 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 ...

  4. 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.

  5. 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.

  6. Covalent radius - Wikipedia

    en.wikipedia.org/wiki/Covalent_radius

    In principle, the sum of the two covalent radii should equal the covalent bond length between two atoms, R(AB) = r(A) + r(B). Moreover, different radii can be introduced for single, double and triple bonds (r 1, r 2 and r 3 below), in a purely operational sense. These relationships are certainly not exact because the size of an atom is not ...

  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. Bond order - Wikipedia

    en.wikipedia.org/wiki/Bond_order

    In carbon monoxide, − C≡O +, the bond order between carbon and oxygen is 3. In thiazyl trifluoride N≡SF 3, the bond order between sulfur and nitrogen is 3, and between sulfur and fluorine is 1. In diatomic oxygen O=O the bond order is 2 (double bond). In ethylene H 2 C=CH 2 the bond order between the two carbon atoms is also 2. The bond ...

  9. Buckminsterfullerene - Wikipedia

    en.wikipedia.org/wiki/Buckminsterfullerene

    The 6:6 ring bonds (between two hexagons) can be considered "double bonds" and are shorter than the 6:5 bonds (between a hexagon and a pentagon). Its average bond length is 0.14 nm. Each carbon atom in the structure is bonded covalently with 3 others. [30] A carbon atom in the C 60 can be substituted by a nitrogen or boron atom yielding a C