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  2. 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).

  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. Newman projection - Wikipedia

    en.wikipedia.org/wiki/Newman_projection

    3D structure A Newman projection is a drawing that helps visualize the 3-dimensional structure of a molecule. [ 1 ] This projection most commonly sights down a carbon-carbon bond, making it a very useful way to visualize the stereochemistry of alkanes.

  5. 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 ...

  6. 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.

  7. 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 ...

  8. Ring flip - Wikipedia

    en.wikipedia.org/wiki/Ring_flip

    Structure D (10.8 kcal/mol) is the highest energy transition state of the process. The molecular motions involved in a chair flip are detailed in the figure on the right: The half-chair conformation ( D , 10.8 kcal/mol, C 2 symmetry) is the energy maximum when proceeding from the chair conformer ( A , 0 kcal/mol reference, D 3d symmetry) to the ...

  9. 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