When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    Cyclohexane is a cycloalkane with the molecular formula ... The conformation of a flat 2D planar hexagon has considerable angle strain because its bonds are not 109. ...

  3. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    A cyclohexane molecule in chair conformation. Hydrogen atoms in axial positions are shown in red, while those in equatorial positions are in blue. Cyclohexane conformations are any of several three-dimensional shapes adopted by molecules of cyclohexane. Because many compounds feature structurally similar six-membered rings, the structure and ...

  4. Cyclic compound - Wikipedia

    en.wikipedia.org/wiki/Cyclic_compound

    Cyclic compounds may or may not exhibit aromaticity; benzene is an example of an aromatic cyclic compound, while cyclohexane is non-aromatic. In organic chemistry, the term aromaticity is used to describe a cyclic (ring-shaped), planar (flat) molecule that exhibits unusual stability as compared to other geometric or connective arrangements of ...

  5. Cyclohexene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene

    Cyclohexene is most stable in a half-chair conformation, [11] unlike the preference for a chair form of cyclohexane. One basis for the cyclohexane conformational preference for a chair is that it allows each bond of the ring to adopt a staggered conformation. For cyclohexene, however, the alkene is planar, equivalent to an eclipsed conformation ...

  6. Anti-periplanar - Wikipedia

    en.wikipedia.org/wiki/Anti-periplanar

    An important factor in the antiperiplanar conformer is the interaction between molecular orbitals. Anti-periplanar geometry will put a bonding orbital and an anti-bonding orbital approximately parallel to each other, or syn-periplanar.

  7. Conformational isomerism - Wikipedia

    en.wikipedia.org/wiki/Conformational_isomerism

    Conformational isomerism. Rotation about single bond of butane to interconvert one conformation to another. The gauche conformation on the right is a conformer, while the eclipsed conformation on the left is a transition state between conformers. Above: Newman projection; below: depiction of spatial orientation.

  8. Hückel's rule - Wikipedia

    en.wikipedia.org/wiki/Hückel's_rule

    Hückel's rule. Benzene, the most widely recognized aromatic compound with six delocalized π-electrons (4 n + 2, for n = 1). In organic chemistry, Hückel's rule predicts that a planar ring molecule will have aromatic properties if it has 4 n + 2 π-electrons, where n is a non-negative integer. The quantum mechanical basis for its formulation ...

  9. Structural formula - Wikipedia

    en.wikipedia.org/wiki/Structural_formula

    Skeletal structural formula of Vitamin B 12.Many organic molecules are too complicated to be specified by a molecular formula.. The structural formula of a chemical compound is a graphic representation of the molecular structure (determined by structural chemistry methods), showing how the atoms are possibly arranged in the real three-dimensional space.