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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 CahnIngoldPrelog (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 CahnIngoldPrelog 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...

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  5. Atropisomer - Wikipedia

    en.wikipedia.org/wiki/Atropisomer

    Alternately, all four groups can be ranked by CahnIngoldPrelog 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]

  6. Allenes - Wikipedia

    en.wikipedia.org/wiki/Allenes

    Where A has a greater priority than B according to the CahnIngoldPrelog priority rules, the configuration of the axial chirality can be determined by considering the substituents on the front atom followed by the back atom when viewed along the allene axis. For the back atom, only the group of higher priority need be considered.

  7. CIP - Wikipedia

    en.wikipedia.org/wiki/CIP

    CahnIngoldPrelog priority rules, or CIP system, for naming organic molecules Carbon in pulp , method of gold extraction Clean-in-place , without disassembly

  8. E–Z notation - Wikipedia

    en.wikipedia.org/wiki/E–Z_notation

    E–Z configuration, or the E–Z convention, is the IUPAC preferred method of describing the absolute stereochemistry of double bonds in organic chemistry.It is an extension of cis–trans isomer notation (which only describes relative stereochemistry) that can be used to describe double bonds having two, three or four substituents.

  9. Talk:Cahn–Ingold–Prelog priority rules - Wikipedia

    en.wikipedia.org/wiki/Talk:CahnIngoldPrelog...

    The Buergenstock Declaration, signed by Cahn, Ingold, and Prelog, as well as 2 others attending the stereochemistry conference held in Buergenstock, Switzerland in 1966, does not appear to have had any role in "laying down the rules" of the CIP conventions. These were put forth in the articles referenced elsewhere on the page.