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  2. Orbital hybridisation - Wikipedia

    en.wikipedia.org/wiki/Orbital_hybridisation

    In ethene, the two carbon atoms form a σ bond by overlapping one sp 2 orbital from each carbon atom. The π bond between the carbon atoms perpendicular to the molecular plane is formed by 2p–2p overlap. Each carbon atom forms covalent C–H bonds with two hydrogens by s–sp 2 overlap, all with 120° bond angles. The hydrogen–carbon bonds ...

  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. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    The polar substituent constants are similar in principle to σ values from the Hammett equation, as an increasing value corresponds to a greater electron-withdrawing ability. Bent's rule suggests that as the electronegativity of the groups increase, more p character is diverted towards those groups, which leaves more s character in the bond ...

  6. Carbon–carbon bond - Wikipedia

    en.wikipedia.org/wiki/Carboncarbon_bond

    In ethane, the orbitals are sp 3-hybridized orbitals, but single bonds formed between carbon atoms with other hybridizations do occur (e.g. sp 2 to sp 2). In fact, the carbon atoms in the single bond need not be of the same hybridization. Carbon atoms can also form double bonds in compounds called alkenes or triple bonds in compounds called ...

  7. Triple bond - Wikipedia

    en.wikipedia.org/wiki/Triple_bond

    Triple bonding can be explained in terms of orbital hybridization. In the case of acetylene, each carbon atom has two sp-orbitals and two p-orbitals. The two sp-orbitals are linear, with 180° bond angles, and occupy the x-axis in the cartesian coordinate system. The p-orbitals are perpendicular to the sp-orbitals on the y-axis and the z-axis.

  8. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    Carbon dioxide (CO 2) has two polar C=O bonds, but the geometry of CO 2 is linear so that the two bond dipole moments cancel and there is no net molecular dipole moment; the molecule is nonpolar. In methane , the bonds are arranged symmetrically (in a tetrahedral arrangement) so there is no overall dipole.

  9. Carbyne - Wikipedia

    en.wikipedia.org/wiki/Carbyne

    The 3σ is a carbon non-bonding orbital pointing along the C–H axis away from the hydrogen, while there are two non-bonding 1π orbitals perpendicular to the C–H axis. However the 3σ is an sp hybrid which has lower energy than the 1π orbital which is pure p, so the 3σ is filled before the 1π.