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  2. Orbital hybridisation - Wikipedia

    en.wikipedia.org/wiki/Orbital_hybridisation

    Chemist Linus Pauling first developed the hybridisation theory in 1931 to explain the structure of simple molecules such as methane (CH 4) using atomic orbitals. [2] Pauling pointed out that a carbon atom forms four bonds by using one s and three p orbitals, so that "it might be inferred" that a carbon atom would form three bonds at right angles (using p orbitals) and a fourth weaker bond ...

  3. Isovalent hybridization - Wikipedia

    en.wikipedia.org/wiki/Isovalent_hybridization

    For example, the C−H bond length is 110.2 pm in ethane, 108.5 pm in ethylene and 106.1 pm in acetylene, with carbon hybridizations sp 3 (25% s), sp 2 (33% s) and sp (50% s) respectively. To determine the degree of hybridization of each bond one can utilize a hybridization parameter (λ).

  4. Carbon–hydrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–hydrogen_bond

    The length of the carbonhydrogen bond varies slightly with the hybridisation of the carbon atom. A bond between a hydrogen atom and an sp 2 hybridised carbon atom is about 0.6% shorter than between hydrogen and sp 3 hybridised carbon. A bond between hydrogen and sp hybridised carbon is shorter still, about 3% shorter than sp 3 C-H.

  5. Valence bond theory - Wikipedia

    en.wikipedia.org/wiki/Valence_bond_theory

    Hybridization is a model that describes how atomic orbitals combine to form new orbitals that better match the geometry of molecules. Atomic orbitals that are similar in energy combine to make hybrid orbitals. For example, the carbon in methane (CH 4) undergoes sp 3 hybridization to form four equivalent orbitals, resulting in a tetrahedral shape.

  6. 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.

  7. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    Carbon and each oxygen atom will have a 2s atomic orbital and a 2p atomic orbital, where the p orbital is divided into p x, p y, and p z. With these derived atomic orbitals, symmetry labels are deduced with respect to rotation about the principal axis which generates a phase change, pi bond ( π ) [ 26 ] or generates no phase change, known as a ...

  8. Carbon–carbon bond - Wikipedia

    en.wikipedia.org/wiki/Carboncarbon_bond

    On the opposite extreme, the central carboncarbon single bond of diacetylene is very strong at 160 kcal/mol, as the single bond joins two carbons of sp hybridization. [9] Carboncarbon multiple bonds are generally stronger; the double bond of ethylene and triple bond of acetylene have been determined to have bond dissociation energies of ...

  9. Acetylene - Wikipedia

    en.wikipedia.org/wiki/Acetylene

    Acetylene (systematic name: ethyne) is the chemical compound with the formula C 2 H 2 and structure H−C≡C−H.It is a hydrocarbon and the simplest alkyne. [8] This colorless gas is widely used as a fuel and a chemical building block.