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  2. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    The axial–equatorial equilibria (A values) are however strongly affected by the replacement of a methylene by O or NH. Illustrative are the conformations of the glucosides. [2] 1,2,4,5-Tetrathiane ((SCH 2) 3) lacks the unfavorable 1,3-diaxial interactions of cyclohexane. Consequently its twist-boat conformation is populated; in the ...

  3. 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 ...

  4. A value - Wikipedia

    en.wikipedia.org/wiki/A_value

    A-values help predict the conformation of cyclohexane rings. The most stable conformation will be the one which has the substituent or substituents equatorial. When multiple substituents are taken into consideration, the conformation where the substituent with the largest A-value is equatorial is favored.

  5. File:Cyclohexane ring flip.svg - Wikipedia

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

    2: half-chair (highest in energy) 3: twist-boat 4: boat When ring flip happens completely from chair-to-chair, hydrogens that were previously axial (blue H) turn equatorial & equatorial ones (red H) turn axial. Pink and orange arrows show how one can imagine how carbons are being "pushed" as one conformation turns into another.

  6. File:Cyclohexane with H.svg - Wikipedia

    en.wikipedia.org/wiki/File:Cyclohexane_with_H.svg

    Chemical structure of cyclohexane, with indication of axial (red) and equatorial (blue) bonds by colors. Date: 30 July 2006: Source: Selfmade with ChemDraw. Author: Calvero. Permission (Reusing this file) PD. Other versions: Image:Cyclohexane structure.png.

  7. File:Axial-equatorial Cyclohexane V.1.svg - Wikipedia

    en.wikipedia.org/wiki/File:Axial-equatorial...

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  8. Ring flip - Wikipedia

    en.wikipedia.org/wiki/Ring_flip

    An example is cyclopropane which, because of its planar geometry, has six fully eclipsed carbon and axial hydrogen bonds making the strain 116 kJ/mol (27.7 kcal/mol). [5] Strain can also be decreased when the carbon-carbon bond angles are close or at the preferred bond angle of 109.5°, meaning a ring having six tetrahedral carbons is typically ...

  9. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    Cyclohexane is a colourless, flammable liquid with a distinctive detergent-like odor, reminiscent of cleaning products (in which it is sometimes used). Cyclohexane is mainly used for the industrial production of adipic acid and caprolactam, which are precursors to nylon. [5] Cyclohexyl (C 6 H 11) is the alkyl substituent of cyclohexane and is ...

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