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  2. Cahn–Ingold–Prelog priority rules - Wikipedia

    en.wikipedia.org/wiki/CahnIngoldPrelog...

    In red is the substituent which determines the final priority. In organic chemistry, the Cahn–IngoldPrelog (CIP) sequence rules (also the CIP priority convention; named after Robert Sidney Cahn, Christopher Kelk Ingold, and Vladimir Prelog) are a standard process to completely and unequivocally name a stereoisomer of a molecule.

  3. Absolute configuration - Wikipedia

    en.wikipedia.org/wiki/Absolute_configuration

    Absolute configuration uses a set of rules to describe the relative positions of each bond around the chiral center atom. The most common labeling method uses the descriptors R or S and is based on the Cahn–IngoldPrelog priority rules. R and S refer to rectus and sinister, Latin for right and left, respectively.

  4. Category:Eponymous chemical rules - Wikipedia

    en.wikipedia.org/wiki/Category:Eponymous...

    Pages in category "Eponymous chemical rules" The following 22 pages are in this category, out of 22 total. ... Cahn–IngoldPrelog priority rules; F. Fajans' rules ...

  5. Robert Sidney Cahn - Wikipedia

    en.wikipedia.org/wiki/Robert_Sidney_Cahn

    Robert Sidney Cahn (9 June 1899 – 15 June 1981) was a British chemist, best known for his contributions to chemical nomenclature and stereochemistry, particularly by the Cahn–IngoldPrelog priority rules, which he proposed in 1956 with Christopher Kelk Ingold and Vladimir Prelog. [1] Cahn was the first to report the structure of ...

  6. Stereocenter - Wikipedia

    en.wikipedia.org/wiki/Stereocenter

    The Cahn-Ingold-Prelog (CIP) system uses R and S designations to define the configuration of atoms about any stereocenter. [7] A designation of R denotes a clockwise direction of substituent priority around the stereocenter, while a designation of S denotes a counter-clockwise direction of substituent priority. [7]

  7. Atropisomer - Wikipedia

    en.wikipedia.org/wiki/Atropisomer

    Alternately, all four groups can be ranked by Cahn–IngoldPrelog priority rules, with overall priority given to the two groups on the "front" atom of the Newman projection. The two configurations determined in this way are termed R a and S a, in analogy to the traditional R/S for a traditional tetrahedral stereocenter. [12]

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  9. Axial chirality - Wikipedia

    en.wikipedia.org/wiki/Axial_chirality

    The designations are based on the same Cahn–IngoldPrelog priority rules used for tetrahedral stereocenters. [3] The chiral axis is viewed end-on and the two "near" and two "far" substituents on the axial unit are ranked, but with the additional rule that the two near substituents have higher priority than the far ones. [4]