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  2. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    Structures of the two enantiomeric forms (S left, R right) of mecoprop Enantiomers of citalopram. The top is (R)-citalopram and the bottom is -citalopram. An example of such an enantiomer is the sedative thalidomide, which was sold in a number of countries around the world from 1957 until 1961. It was withdrawn from the market when it was found ...

  3. Absolute configuration - Wikipedia

    en.wikipedia.org/wiki/Absolute_configuration

    The R/S system is an important nomenclature system for denoting enantiomers. This approach labels each chiral center R or S according to a system by which its substituents are each assigned a priority, according to the Cahn–Ingold–Prelog priority rules (CIP), based on atomic number.

  4. Gas constant - Wikipedia

    en.wikipedia.org/wiki/Gas_constant

    T is the temperature, T TPW = 273.16 K by the definition of the kelvin at that time; A r (Ar) is the relative atomic mass of argon and M u = 10 −3 kg⋅mol −1 as defined at the time. However, following the 2019 revision of the SI , R now has an exact value defined in terms of other exactly defined physical constants.

  5. Chirality - Wikipedia

    en.wikipedia.org/wiki/Chirality

    In physics, chirality may be found in the spin of a particle, where the handedness of the object is determined by the direction in which the particle spins. [4] Not to be confused with helicity , which is the projection of the spin along the linear momentum of a subatomic particle, chirality is an intrinsic quantum mechanical property, like spin.

  6. Chirality (chemistry) - Wikipedia

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

    Two enantiomers of a generic amino acid that are chiral (S)-Alanine (left) and (R)-alanine (right) in zwitterionic form at neutral pH. In chemistry, a molecule or ion is called chiral (/ ˈ k aɪ r əl /) if it cannot be superposed on its mirror image by any combination of rotations, translations, and some conformational changes.

  7. Optical rotation - Wikipedia

    en.wikipedia.org/wiki/Optical_rotation

    If two enantiomers are present in equal proportions, then their effects cancel out and no optical activity is observed; this is termed a racemic mixture. But when there is an enantiomeric excess, more of one enantiomer than the other, the cancellation is incomplete and optical activity is observed. Many naturally occurring molecules are present ...

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  9. Chiral media - Wikipedia

    en.wikipedia.org/wiki/Chiral_media

    Chirality with hands and two enantiomers of a generic amino acid The direction of current flow and induced magnetic flux follow a "handness" relationship. The term chiral / ˈ k aɪ r əl / describes an object, especially a molecule, which has or produces a non-superposable mirror image of itself.