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  2. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    The staggered conformation is more stable by 12.5 kJ/mol than the eclipsed conformation, which is the energy maximum for ethane. In the eclipsed conformation the torsional angle is minimised. staggered conformation left, eclipsed conformation right in Newman projection

  3. File:Ethane conformations and relative energies.svg - Wikipedia

    en.wikipedia.org/wiki/File:Ethane_conformations...

    B is highest & A lowest in energy. A is thus the most stable conformation. Valleys are local energy minima. A can thus be classified as a rotamer (a class of conformers). Peaks are not rotamers, & are caused by repulsive forces of the hydrogens. Source for conformation names & rotamer classification:

  4. Standard Gibbs free energy of formation - Wikipedia

    en.wikipedia.org/wiki/Standard_Gibbs_free_energy...

    The standard Gibbs free energy of formation (G f °) of a compound is the change of Gibbs free energy that accompanies the formation of 1 mole of a substance in its standard state from its constituent elements in their standard states (the most stable form of the element at 1 bar of pressure and the specified temperature, usually 298.15 K or 25 °C).

  5. 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 ...

  6. Standard enthalpy of formation - Wikipedia

    en.wikipedia.org/wiki/Standard_enthalpy_of_formation

    For elements that have multiple allotropes, the reference state usually is chosen to be the form in which the element is most stable under 1 bar of pressure. One exception is phosphorus, for which the most stable form at 1 bar is black phosphorus, but white phosphorus is chosen as the standard reference state for zero enthalpy of formation. [2]

  7. Gauche effect - Wikipedia

    en.wikipedia.org/wiki/Gauche_effect

    The gauche effect is very sensitive to solvent effects, due to the large difference in polarity between the two conformers.For example, 2,3-dinitro-2,3-dimethylbutane, which in the solid state exists only in the gauche conformation, prefers the gauche conformer in benzene solution by a ratio of 79:21, but in carbon tetrachloride, it prefers the anti conformer by a ratio of 58:42. [9]

  8. Eclipsed conformation - Wikipedia

    en.wikipedia.org/wiki/Eclipsed_conformation

    It was found that the most stable conformations had lower energies based on values of energy due to bond distances and bond angles. [ 6 ] In many cases, isomers of alkanes with branched chains have lower boiling points than those that are unbranched, which has been shown through experimentation with isomers of C 8 H 18 .

  9. Chemical stability - Wikipedia

    en.wikipedia.org/wiki/Chemical_stability

    Chemical substances or states can persist indefinitely even though they are not in their lowest energy state if they experience metastability - a state which is stable only if not disturbed too much. A substance (or state) might also be termed "kinetically persistent" if it is changing relatively slowly (and thus is not at thermodynamic ...