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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. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    In traditional hybridisation theory, the hybrid orbitals are all equivalent. [12] [27] Namely the atomic s and p orbital(s) are combined to give four sp i 3 = 1 ⁄ √ 4 (s + √ 3 p i) orbitals, three sp i 2 = 1 ⁄ √ 3 (s + √ 2 p i) orbitals, or two sp i = 1 ⁄ √ 2 (s + p i) orbitals. These combinations are chosen to satisfy two ...

  4. Carbanion - Wikipedia

    en.wikipedia.org/wiki/Carbanion

    Absent π delocalization, the negative charge of a carbanion is localized in an sp x hybridized orbital on carbon as a lone pair.As a consequence, localized alkyl, alkenyl/aryl, and alkynyl carbanions assume trigonal pyramidal, bent, and linear geometries, respectively.

  5. Carbon–carbon bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–carbon_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 ...

  6. Orbital overlap - Wikipedia

    en.wikipedia.org/wiki/Orbital_overlap

    In chemical bonds, an orbital overlap is the concentration of orbitals on adjacent atoms in the same regions of space. Orbital overlap can lead to bond formation. Linus Pauling explained the importance of orbital overlap in the molecular bond angles observed through experimentation; it is the basis for orbital hybridization.

  7. Tertiary carbon - Wikipedia

    en.wikipedia.org/wiki/Tertiary_carbon

    Additionally, the surrounding sp3 hybridized carbons can stabilize the carbocation through hyperconjugation. [5] This occurs when adjacent sp3 orbitals have a weak overlap with the vacant p orbital; since there are 3 surrounding carbons with sp3 hybridization , there are more opportunities for overlap, which contributes to increasing ...

  8. Isovalent hybridization - Wikipedia

    en.wikipedia.org/wiki/Isovalent_hybridization

    In chemistry, isovalent or second order hybridization is an extension of orbital hybridization, the mixing of atomic orbitals into hybrid orbitals which can form chemical bonds, to include fractional numbers of atomic orbitals of each type (s, p, d). It allows for a quantitative depiction of bond formation when the molecular geometry deviates ...

  9. 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.