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  2. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    A monosubstituted cyclohexane is one in which there is one non-hydrogen substituent in the cyclohexane ring. The most energetically favorable conformation for a monosubstituted cyclohexane is the chair conformation with the non-hydrogen substituent in the equatorial position because it prevents high steric strain from 1,3 diaxial interactions. [10]

  3. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    Cyclohexane is a cycloalkane with the molecular formula C 6 H 12. Cyclohexane is non-polar . Cyclohexane is a colourless, flammable liquid with a distinctive detergent -like odor, reminiscent of cleaning products (in which it is sometimes used).

  4. A value - Wikipedia

    en.wikipedia.org/wiki/A_value

    A methyl substituent has a significantly smaller A-value than a tert-butyl substituent; therefore the most stable conformation has the tert-butyl in the equatorial position. The utility of A-values can be generalized for use outside of cyclohexane conformations. A-values can help predict the steric effect of a substituent. In general, the ...

  5. File:Cyclohexane ring flip and relative conformation energies ...

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

    This image of a simple chemical equation is ineligible for copyright and therefore in the public domain, because it consists entirely of information that is common property and contains no original authorship.

  6. Cyclohexene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene

    Cyclohexene is most stable in a half-chair conformation, [11] unlike the preference for a chair form of cyclohexane. One basis for the cyclohexane conformational preference for a chair is that it allows each bond of the ring to adopt a staggered conformation. For cyclohexene, however, the alkene is planar, equivalent to an eclipsed conformation ...

  7. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    The strain energy of a cycloalkane is the increase in energy caused by the compound's geometry, and is calculated by comparing the experimental standard enthalpy change of combustion of the cycloalkane with the value calculated using average bond energies. Molecular mechanics calculations are well suited to identify the many conformations ...

  8. Rotamers - Wikipedia

    en.wikipedia.org/wiki/Chemical_conformation

    The repulsion between an axial t-butyl group and hydrogen atoms in the 1,3-diaxial position is so strong that the cyclohexane ring will revert to a twisted boat conformation. The strain in cyclic structures is usually characterized by deviations from ideal bond angles ( Baeyer strain ), ideal torsional angles ( Pitzer strain ) or transannular ...

  9. Cyclohexane (data page) - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_(data_page)

    Otherwise value is equilibrium temperature of vapor over liquid. log 10 of Cyclohexane vapor pressure. Uses formula: ...