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  2. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    Cis-1,4-Di-tert-butylcyclohexane has an axial tert-butyl group in the chair conformation and conversion to the twist-boat conformation places both groups in more favorable equatorial positions. As a result, the twist-boat conformation is more stable by 0.47 kJ/mol (0.11 kcal/mol) at 125 K (−148 °C) as measured by NMR spectroscopy. [9]

  3. Rotamers - Wikipedia

    en.wikipedia.org/wiki/Rotamers

    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 ...

  4. Fluxional molecule - Wikipedia

    en.wikipedia.org/wiki/Fluxional_molecule

    Cyclohexane chair flip (ring inversion) reaction via boat conformation [8] The interconversion of equivalent chair conformers of cyclohexane (and many other cyclic compounds) is called ring flipping. Carbon–hydrogen bonds that are axial in one configuration become equatorial in the other, and vice versa.

  5. 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.

  6. Structural formula - Wikipedia

    en.wikipedia.org/wiki/Structural_formula

    There is a peak/local maximum at the boat conformation (C), and there are valleys/local minimums at the twist-boat conformations (B). In addition, cyclohexane conformations can be used to indicate if the molecule has any 1,3 diaxial-interactions which are steric interactions between axial substituents on the 1,3, and 5 carbons. [7]

  7. 6 Heart-Healthy Foods You Should be Eating in January ... - AOL

    www.aol.com/6-heart-healthy-foods-eating...

    Heart disease is the No. 1 cause of death in the U.S. Yet, according to the American Heart Association, half of Americans are unaware of this sobering statistic.

  8. File:Cyclohexane ring flip.svg - Wikipedia

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

    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. Source for the conformation names & claim of lowest/highest energy:

  9. College Football Playoff: Who has the best odds to win the title?

    www.aol.com/college-football-playoff-best-odds...

    The first 12-team College Football Playoff field was revealed on Sunday. Undefeated Oregon earned the top seed, while SMU beat out Alabama for the 12th and final spot. Oregon, Georgia, Boise State ...