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  2. Newman projection - Wikipedia

    en.wikipedia.org/wiki/Newman_projection

    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.

  3. Gauche effect - Wikipedia

    en.wikipedia.org/wiki/Gauche_effect

    The gauche effect is very sensitive to solvent effects, due to the large difference in polarity between the two conformers.For example, 2,3-dinitro-2,3-dimethylbutane, which in the solid state exists only in the gauche conformation, prefers the gauche conformer in benzene solution by a ratio of 79:21, but in carbon tetrachloride, it prefers the anti conformer by a ratio of 58:42. [9]

  4. 2,3-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethylpentane

    2,3-Dimethylpentane is notable for being one of the two simplest alkanes with optical (enantiomeric) isomerism. The optical center is the middle carbon of the pentane backbone, which is connected to one hydrogen atom, one methyl group, one ethyl group – C 2 H 5, and one isopropyl group – CH(CH 3) 2.

  5. Anti-periplanar - Wikipedia

    en.wikipedia.org/wiki/Anti-periplanar

    Figure 5 shows 2-chloro-2,3-dimethylbutane in a sawhorse projection with chlorine and a hydrogen anti-periplanar to each other. Syn-periplanar or synperiplanar is similar to anti-periplanar. In the syn-periplanar conformer, the A and D are on the same side of the plane of the bond, with the dihedral angle of A−B and C−D between +30° and ...

  6. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    Above: Newman projection; below: depiction of spatial orientation. In chemistry, rotamers are chemical species that differ from one another primarily due to rotations about one or more single bonds. Various arrangements of atoms in a molecule that differ by rotation about single bonds can also be referred to as different conformations ...

  7. Eclipsed conformation - Wikipedia

    en.wikipedia.org/wiki/Eclipsed_conformation

    The example below is looking down the C2 and C3 bond. Below is the sawhorse and Newman representation of butane in an eclipsed conformation with the two CH 3 groups (C1 and C4) at a 0-degree angle from one another (left). If the front is rotated 60° clockwise, the butane molecule is now in a staggered conformation (right).

  8. 2,3-Dimethylbutane - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethylbutane

    2,3-Dimethylbutane is an isomer of hexane. It has the chemical formula (CH 3) 2 CHCH(CH 3) 2. It is a colorless liquid which boils at 57.9 °C. References

  9. Melvin Spencer Newman - Wikipedia

    en.wikipedia.org/wiki/Melvin_Spencer_Newman

    Melvin Spencer Newman (March 10, 1908 – May 30, 1993) was an American chemist, Ohio State University professor, best known for inventing the Newman projection. Newman was born in New York City in a Jewish family, the youngest of Mae (née Polack) and Jacob K. Newman's four children. [ 1 ]