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  2. Eclipsed conformation - Wikipedia

    en.wikipedia.org/wiki/Eclipsed_conformation

    In the example of ethane, such a graph shows that rotation around the carbon-carbon bond is not entirely free but that an energy barrier exists. The ethane molecule in the eclipsed conformation is said to suffer from torsional strain, and by a rotation around the carbon carbon bond to the staggered conformation around 12.5 kJ/mol of torsional ...

  3. Ethane - Wikipedia

    en.wikipedia.org/wiki/Ethane

    Ethane (US: / ˈ ɛ θ eɪ n / ETH-ayn, UK: / ˈ iː-/ EE-) is a naturally occurring organic chemical compound with chemical formula C 2 H 6. At standard temperature and pressure, ethane is a colorless, odorless gas. Like many hydrocarbons, ethane is isolated on an industrial scale from natural gas and as a petrochemical by-product of petroleum ...

  4. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    The textbook explanation for the existence of the energy maximum for an eclipsed conformation in ethane is steric hindrance, but, with a C-C bond length of 154 pm and a Van der Waals radius for hydrogen of 120 pm, the hydrogen atoms in ethane are never in each other's way. The question of whether steric hindrance is responsible for the eclipsed ...

  5. Molecular binding - Wikipedia

    en.wikipedia.org/wiki/Molecular_binding

    For example, the biotin-streptavidin interaction can be broken by incubating the complex in water at 70 °C, without damaging either molecule. [6] An example of change in local concentration causing dissociation can be found in the Bohr effect , which describes the dissociation of ligands from hemoglobin in the lung versus peripheral tissues.

  6. Carbon–hydrogen bond activation - Wikipedia

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

    In organic chemistry and organometallic chemistry, carbon–hydrogen bond activation (C−H activation) is a type of organic reaction in which a carbon–hydrogen bond is cleaved and replaced with a C−X bond (X ≠ H is typically a main group element, like carbon, oxygen, or nitrogen).

  7. Carbon–carbon bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–carbon_bond

    Carbon is one of the few elements that can form long chains of its own atoms, a property called catenation.This coupled with the strength of the carbon–carbon bond gives rise to an enormous number of molecular forms, many of which are important structural elements of life, so carbon compounds have their own field of study: organic chemistry.

  8. Catenation - Wikipedia

    en.wikipedia.org/wiki/Catenation

    In organic chemistry, hydrogen bonding is known to facilitate the formation of chain structures. For example, 4-tricyclanol C 10 H 16 O shows catenated hydrogen bonding between the hydroxyl groups, leading to the formation of helical chains; [4] crystalline isophthalic acid C 8 H 6 O 4 is built up from molecules connected by hydrogen bonds ...

  9. 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.