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  2. Transition metal alkene complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_alkene...

    The bonding between alkenes and transition metals is described by the Dewar–Chatt–Duncanson model, which involves donation of electrons in the pi-orbital on the alkene to empty orbitals on the metal. This interaction is reinforced by back bonding that entails sharing of electrons in other metal orbitals into the empty pi-antibonding level ...

  3. Dewar–Chatt–Duncanson model - Wikipedia

    en.wikipedia.org/wiki/Dewar–Chatt–Duncanson...

    On the left, a filled pi-orbital on C 2 H 4 overlaps with an empty d-orbital on the metal. On the right, an empty pi-antibonding orbital on C 2 H 4 overlaps with a filled d-orbital on the metal The Dewar–Chatt–Duncanson model is a model in organometallic chemistry that explains the chemical bonding in transition metal alkene complexes .

  4. Frontier molecular orbital theory - Wikipedia

    en.wikipedia.org/wiki/Frontier_molecular_orbital...

    Since the exo-product has primary (bonding) orbital interactions, it can still form; but since the endo-product forms faster, it is the major product. [2] *Note: The HOMO of ethene and the LUMO of butadiene are both symmetric, meaning the reaction between these species is allowed as well. This is referred to as the "inverse electron demand ...

  5. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    The possible orbital symmetries are listed in the table below. For example, an orbital of B 1 symmetry (called a b 1 orbital with a small b since it is a one-electron function) is multiplied by -1 under the symmetry operations C 2 (rotation about the 2-fold rotation axis) and σ v '(yz) (reflection in the molecular

  6. Molecular orbital - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital

    Complete acetylene (H–C≡C–H) molecular orbital set. The left column shows MO's which are occupied in the ground state, with the lowest-energy orbital at the top. The white and grey line visible in some MO's is the molecular axis passing through the nuclei. The orbital wave functions are positive in the red regions and negative in the blue.

  7. Pi bond - Wikipedia

    en.wikipedia.org/wiki/Pi_bond

    Ethylene (ethene), a small organic molecule containing a pi bond, shown in green.. In chemistry, pi bonds (π bonds) are covalent chemical bonds, in each of which two lobes of an orbital on one atom overlap with two lobes of an orbital on another atom, and in which this overlap occurs laterally.

  8. Hückel method - Wikipedia

    en.wikipedia.org/wiki/Hückel_method

    The method predicts how many energy levels exist for a given molecule, which levels are degenerate and it expresses the molecular orbital energies in terms of two parameters, called α, the energy of an electron in a 2p orbital, and β, the interaction energy between two 2p orbitals (the extent to which an electron is stabilized by allowing it ...

  9. Ethane - Wikipedia

    en.wikipedia.org/wiki/Ethane

    The chief use of ethane is the production of ethylene (ethene) by steam cracking. Steam cracking of ethane is fairly selective for ethylene, while the steam cracking of heavier hydrocarbons yields a product mixture poorer in ethylene and richer in heavier alkenes (olefins), such as propene (propylene) and butadiene, and in aromatic hydrocarbons.