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  2. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    The chair and twist-boat are energy minima and are therefore conformers, while the half-chair and the boat are transition states and represent energy maxima. The idea that the chair conformation is the most stable structure for cyclohexane was first proposed as early as 1890 by Hermann Sachse, but only gained widespread acceptance much later.

  3. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    Cyclohexane conformations are any of several three-dimensional shapes adopted by cyclohexane. Because many compounds feature structurally similar six-membered rings , the structure and dynamics of cyclohexane are important prototypes of a wide range of compounds.

  4. Cyclohexane (data page) - Wikipedia

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

    Structure and properties Index of refraction, n D: 1.4262 at 20 °C ... for Cyclohexane/Acetic acid [6] P = 101.325 kPa BP Temp. °C % by mole acetic acid liquid

  5. Ring flip - Wikipedia

    en.wikipedia.org/wiki/Ring_flip

    Cyclohexane is a prototype for low-energy degenerate ring flipping. Two 1 H NMR signals should be observed in principle, corresponding to axial and equatorial protons. However, due to the cyclohexane chair flip, only one signal is seen for a solution of cyclohexane at room temperature, as the axial and equatorial proton rapidly interconvert ...

  6. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    Cyclohexane conformations, including with chair and boat conformations among others. Cycloalkane conformations, including medium rings and macrocycles; Carbohydrate conformation, which includes cyclohexane conformations as well as other details. Allylic strain – energetics related to rotation about the single bond between an sp 2 carbon and ...

  7. Hexachlorocyclohexane - Wikipedia

    en.wikipedia.org/wiki/Hexachlorocyclohexane

    They have been used as models for analyzing the effects of different geometric positions of the large atoms with dipolar bonds on the stability of the cyclohexane conformation. [1] The isomers are poisonous, pesticidal, and persistent organic pollutants, to varying degrees. Hexachlorocyclohexane was dimerized to produce mirex, a banned pesticide.

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

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

    English: Cyclohexane chair flip (ring inversion) reaction. Structures of the significant conformations (A, B, C & D) of the reaction are shown & plotted against their ...