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  2. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    The chair conformation is the most stable conformer. At 298 K (25 °C), 99.99% of all molecules in a cyclohexane solution adopt this conformation. The C–C ring of the chair conformation has the same shape as the 6-membered rings in the diamond cubic lattice. [7]: 16 This can be modeled as follows.

  3. Ring flip - Wikipedia

    en.wikipedia.org/wiki/Ring_flip

    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 higher energy twist-boat conformer (B, 5.5 kcal/mol, D 2 symmetry).

  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. Methylcyclohexane - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexane

    Most methylcyclohexane is extracted from petroleum but it can be also produced by catalytic hydrogenation of toluene: CH 3 C 6 H 5 + 3 H 2 → CH 3 C 6 H 11. The hydrocarbon is a minor component of automobile fuel, with its share in US gasoline varying between 0.3 and 1.7% in early 1990s [10] and 0.1 to 1% in 2011. [11]

  6. Menthol - Wikipedia

    en.wikipedia.org/wiki/Menthol

    The (+)- and (−)-enantiomers of menthol are the most stable among these based on their cyclohexane conformations. With the ring itself in a chair conformation, all three bulky groups can orient in equatorial positions. The two crystal forms for racemic menthol have melting points of 28 °C and 38 °C. Pure (−)-menthol has four crystal forms ...

  7. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    In the most stable chair form of cyclohexane, axial hydrogens on adjacent carbon atoms are pointed in opposite directions, virtually eliminating eclipsing strain. In medium-sized rings (7 to 13 carbon atoms) conformations in which the angle strain is minimised create transannular strain or Pitzer strain .

  8. Why Marlee Matlin Calls Longtime Friend Henry Winkler Her ...

    www.aol.com/lifestyle/why-marlee-matlin-calls...

    Not Alone Anymore chronicles Matlin’s journey from her breakout as the youngest and first deaf best actress Academy Award winner, to the years following, when she fought for cultural ...

  9. Fürst-Plattner Rule - Wikipedia

    en.wikipedia.org/wiki/Fürst-Plattner_Rule

    The Fürst-Plattner rule attributes this regiochemical control to a large preference for the reaction pathway that follows the more stable chair-like transition state (attack at the C1-position) compared to the one proceeding through the unfavored twist boat-like transition state (attack at the C2-position).