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  2. Newman projection - Wikipedia

    en.wikipedia.org/wiki/Newman_projection

    A Newman projection visualizes the conformation of a chemical bond from front to back, with the front atom represented by the intersection of three lines (a dot) and the back atom as a circle. The front atom is called proximal , while the back atom is called distal .

  3. Anti-periplanar - Wikipedia

    en.wikipedia.org/wiki/Anti-periplanar

    In a Newman projection, the molecule will be in a staggered arrangement with the anti-periplanar functional groups pointing up and down, 180° away from each other (see Figure 4). Figure 5 shows 2-chloro-2,3-dimethylbutane in a sawhorse projection with chlorine and a hydrogen anti-periplanar to each other.

  4. Asymmetric induction - Wikipedia

    en.wikipedia.org/wiki/Asymmetric_induction

    The Cram's rule of asymmetric induction named after Donald J. Cram states In certain non-catalytic reactions that diastereomer will predominate, which could be formed by the approach of the entering group from the least hindered side when the rotational conformation of the C-C bond is such that the double bond is flanked by the two least bulky groups attached to the adjacent asymmetric center. [3]

  5. 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.

  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

    In chemistry an eclipsed conformation is a conformation in which two substituents X and Y on adjacent atoms A, B are in closest proximity, implying that the torsion angle X–A–B–Y is 0°. [1] Such a conformation can exist in any open chain, single chemical bond connecting two sp 3 - hybridised atoms, and it is normally a conformational ...

  8. Heather Locklear Calls Out the Differences Between ... - AOL

    www.aol.com/lifestyle/heather-locklear-calls...

    The ABC sitcom originally starred Michael J. Fox, who left the show after four seasons following his Parkinson's diagnosis and was replaced by Charlie Sheen

  9. Flippin–Lodge angle - Wikipedia

    en.wikipedia.org/wiki/Flippin–Lodge_angle

    The Flippin–Lodge angle is one of two angles used by organic and biological chemists studying the relationship between a molecule's chemical structure and ways that it reacts, for reactions involving "attack" of an electron-rich reacting species, the nucleophile, on an electron-poor reacting species, the electrophile.