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  2. Eclipsed conformation - Wikipedia

    en.wikipedia.org/wiki/Eclipsed_conformation

    In the case of butane and its four-carbon chain, three carbon-carbon bonds are available to rotate. The example below is looking down the C2 and C3 bond. Below is the sawhorse and Newman representation of butane in an eclipsed conformation with the two CH 3 groups (C1 and C4) at a 0-degree angle from one another (left).

  3. Chemical bond - Wikipedia

    en.wikipedia.org/wiki/Chemical_bond

    A chemical bond is the association of atoms or ions to form molecules, crystals, and other structures. The bond may result from the electrostatic force between oppositely charged ions as in ionic bonds or through the sharing of electrons as in covalent bonds, or some combination of these effects.

  4. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    Allylic strain – energetics related to rotation about the single bond between an sp 2 carbon and an sp 3 carbon. Atropisomerism – due to restricted rotation about a bond. Folding, including the secondary and tertiary structure of biopolymers (nucleic acids and proteins). [11] Akamptisomerism – due to restricted inversion of a bond angle.

  5. Bonding in solids - Wikipedia

    en.wikipedia.org/wiki/Bonding_in_solids

    Covalent and ionic bonding form a continuum, with ionic character increasing with increasing difference in the electronegativity of the participating atoms. Covalent bonding corresponds to sharing of a pair of electrons between two atoms of essentially equal electronegativity (for example, C–C and C–H bonds in aliphatic hydrocarbons).

  6. Chemical structure - Wikipedia

    en.wikipedia.org/wiki/Chemical_structure

    Theories of chemical structure were first developed by August Kekulé, Archibald Scott Couper, and Aleksandr Butlerov, among others, from about 1858. [4] These theories were first to state that chemical compounds are not a random cluster of atoms and functional groups, but rather had a definite order defined by the valency of the atoms composing the molecule, giving the molecules a three ...

  7. Three-center four-electron bond - Wikipedia

    en.wikipedia.org/.../Three-center_four-electron_bond

    This exercise generates the diagram at right (Figure 1). Three molecular orbitals result from the combination of the three relevant atomic orbitals, with the four electrons occupying the two MOs lowest in energy – a bonding MO delocalized across all three centers, and a non-bonding MO localized on the peripheral centers.

  8. Molecular binding - Wikipedia

    en.wikipedia.org/wiki/Molecular_binding

    Irreversible covalent – a chemical bond is formed in which the product is thermodynamically much more stable than the reactants such that the reverse reaction does not take place. Bound molecules are sometimes called a "molecular complex"—the term generally refers to non-covalent associations. [ 2 ]

  9. Intramolecular force - Wikipedia

    en.wikipedia.org/wiki/Intramolecular_force

    The bond length, or the minimum separating distance between two atoms participating in bond formation, is determined by their repulsive and attractive forces along the internuclear direction. [3] As the two atoms get closer and closer, the positively charged nuclei repel, creating a force that attempts to push the atoms apart.

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