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  2. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    The twist boat has a lower energy than the boat. In order to go from the chair conformation to a twist-boat conformation or the other chair conformation, bond angles have to be changed, leading to a high-energy half-chair conformation. So the relative stabilities are: chair > twist boat > boat > half-chair. All relative conformational energies ...

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

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

    A is thus the most stable conformation &, of all the other conformations, occurs most often in room temperature. Valleys A & B are local energy minima & A is global minima. A & B can thus be classified as conformers.

  4. Ring flip - Wikipedia

    en.wikipedia.org/wiki/Ring_flip

    The chair conformation minimizes both angle strain and torsional strain by having all carbon-carbon bonds at 110.9° and all hydrogens staggered from one another. [2] The conformational changes that occur in a cyclohexane ring flip take place over several stages. Structure D (10.8 kcal/mol) is the highest energy transition state of the process.

  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:Chair conformation of cyclohexane.svg - Wikipedia

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

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  7. 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.

  8. Structural formula - Wikipedia

    en.wikipedia.org/wiki/Structural_formula

    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] Chair conformation of beta-D-Glucose The cyclohexane conformations in relation to the potential energy at each conformation

  9. 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 ...