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  2. 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 ...

  3. Isovalent hybridization - Wikipedia

    en.wikipedia.org/wiki/Isovalent_hybridization

    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 ...

  4. Carbon–hydrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–hydrogen_bond

    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. This trend is illustrated by the molecular geometry of ethane, ethylene and acetylene. [citation needed]

  5. Tertiary carbon - Wikipedia

    en.wikipedia.org/wiki/Tertiary_carbon

    Tertiary carbon. A tertiary carbon atom is a carbon atom bound to three other carbon atoms. [1] For this reason, tertiary carbon atoms are found only in hydrocarbons containing at least four carbon atoms. They are called saturated hydrocarbons because they only contain carbon-carbon single bonds. [2] Tertiary carbons have a hybridization of sp3.

  6. Orbital hybridisation - Wikipedia

    en.wikipedia.org/wiki/Orbital_hybridisation

    Checked. In chemistry, orbital hybridisation (or hybridization) is the concept of mixing atomic orbitals to form new hybrid orbitals (with different energies, shapes, etc., than the component atomic orbitals) suitable for the pairing of electrons to form chemical bonds in valence bond theory. For example, in a carbon atom which forms four ...

  7. Homolysis (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Homolysis_(chemistry)

    An sp3 hybridized atom is the most stable configuration for a radical because of the low s-character. Orbital hybridization. The s-character of an orbital relates to how close electrons are to the nucleus. In the case of a radical, s-character more specifically relates to how close the single electron is to the nucleus.

  8. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    Alkane. In organic chemistry, an alkane, or paraffin (a historical trivial name that also has other meanings), is an acyclic saturated hydrocarbon. In other words, an alkane consists of hydrogen and carbon atoms arranged in a tree structure in which all the carbon–carbon bonds are single. [1] Alkanes have the general chemical formula CnH2n+2.

  9. Isolobal principle - Wikipedia

    en.wikipedia.org/wiki/Isolobal_principle

    Isolobal principle. In organometallic chemistry, the isolobal principle (more formally known as the isolobal analogy) is a strategy used to relate the structure of organic and inorganic molecular fragments in order to predict bonding properties of organometallic compounds. [1] Roald Hoffmann described molecular fragments as isolobal "if the ...