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  2. Triple bond - Wikipedia

    en.wikipedia.org/wiki/Triple_bond

    A triple bond in chemistry is a chemical bond between two atoms involving six bonding electrons instead of the usual two in a covalent single bond. Triple bonds are stronger than the equivalent single bonds or double bonds, with a bond order of three. The most common triple bond is in a nitrogen N 2 molecule; the second most common is that ...

  3. Carbon–nitrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbonnitrogen_bond

    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] A CN bond is strongly polarized towards nitrogen (the electronegativities of C and N are 2.55 and 3.04, respectively) and subsequently molecular ...

  4. Isocyanide - Wikipedia

    en.wikipedia.org/wiki/Isocyanide

    An isocyanide (also called isonitrile or carbylamine) is an organic compound with the functional group – N + ≡C −. It is the isomer of the related nitrile (–C≡N), hence the prefix is isocyano. [1] The organic fragment is connected to the isocyanide group through the nitrogen atom, not via the carbon. They are used as building blocks ...

  5. Isocyanic acid - Wikipedia

    en.wikipedia.org/wiki/Isocyanic_acid

    Although the electronic structure according to valence bond theory can be written as H−N=C=O, the vibrational spectrum has a band at 2268.8 cm −1 in the gas phase, which some say indicates a carbonnitrogen triple bond. [10] [11] If so, then the canonical form H−N + ≡C−O − is the major resonance structure.

  6. Contact explosive - Wikipedia

    en.wikipedia.org/wiki/Contact_explosive

    Nitro compounds are explosive because although the diatomic form of nitrogen is very stable—that is, the triple bond that holds N 2 together is very strong, and therefore has a great deal of bond energy—the nitro compounds themselves are unstable, as the bonds between nitrogen atoms and other atoms in nitro compounds are weak by comparison.

  7. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    A 3D model of ethyne (), the simplest alkyneIn organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carboncarbon triple bond. [1] The simplest acyclic alkynes with only one triple bond and no other functional groups form a homologous series with the general chemical formula C n H 2n−2.

  8. Transition metal carbyne complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_carbyne...

    This triple bond consists of a σ-bond and two π-bonds. [2] The HOMO of the carbyne ligand interacts with the LUMO of the metal to create the σ-bond. The two π-bonds are formed when the two HOMO orbitals of the metal back-donate to the LUMO of the carbyne. They are also called metal alkylidynes—the carbon is a carbyne ligand.

  9. Lone pair - Wikipedia

    en.wikipedia.org/wiki/Lone_pair

    In Group 14 elements (the carbon group), lone pairs can manifest themselves by shortening or lengthening single bond (bond order 1) lengths, [16] as well as in the effective order of triple bonds as well. [17] [18] The familiar alkynes have a carbon-carbon triple bond (bond order 3) and a linear geometry of 180° bond angles (figure A in ...