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  2. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    trans-1,3-Disubstituted cyclohexanes are like cis-1,2- and cis-1,4- and can flip between the two equivalent axial/equatorial forms. [ 2 ] 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.

  3. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    A: antiperiplanar, anti or trans. B: synclinal or gauche. C: anticlinal or eclipsed. D: synperiplanar or cis. [2] Rotating their carbon–carbon bonds, the molecules ethane and propane have three local energy minima. They are structurally and energetically equivalent, and are called the staggered conformers.

  4. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cistrans_isomerism

    Very often, cistrans stereoisomers contain double bonds or ring structures. In both cases the rotation of bonds is restricted or prevented. [4] When the substituent groups are oriented in the same direction, the diastereomer is referred to as cis, whereas when the substituents are oriented in opposing directions, the diastereomer is referred to as trans.

  5. 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).

  6. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    The most common one in nature (myo-inositol) has the hydroxyls on carbons 1, 2, 3 and 5 on the same side of that plane, and can therefore be called cis-1,2,3,5-trans-4,6-cyclohexanehexol. And each of these cis - trans isomers can possibly have stable "chair" or "boat" conformations (although the barriers between these are significantly lower ...

  7. Cyclooctene - Wikipedia

    en.wikipedia.org/wiki/Cyclooctene

    The cis isomer can adopt various conformations, the most stable one being shaped like a ribbon. [1] The most stable conformation of trans-cyclooctene is shaped like the 8-carbon equivalent of the chair conformation of cyclohexane. Longer cycloalkene rings such as the ten-carbon cyclodecene also occur as cis and trans isomers.

  8. Why Do Mark Gastineau and Brett Favre Have Beef? All ... - AOL

    www.aol.com/why-mark-gastineau-brett-favre...

    There's been a rift between former New York Jets star Mark Gastineau and legendary NFL quarterback Brett Favre since 2002.. Gastineau held the NFL sack record from 1984 to 2001 — an ...

  9. Chirality (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Chirality_(chemistry)

    Similarly, cis-1,2-dichlorocyclohexane consists of chair conformers that are nonidentical mirror images, but the two can interconvert via the cyclohexane chair flip (~10 kcal/mol barrier). As another example, amines with three distinct substituents (R 1 R 2 R 3 N:) are also regarded as achiral molecules because their enantiomeric pyramidal ...