enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Cahn–Ingold–Prelog priority rules - Wikipedia

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

    For double bonded molecules, CahnIngoldPrelog priority rules (CIP rules) are followed to determine the priority of substituents of the double bond. If both of the high priority groups are on the same side of the double bond (cis configuration), then the stereoisomer is assigned the configuration Z (zusammen, German word meaning "together").

  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. 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]

  5. Chiral drugs - Wikipedia

    en.wikipedia.org/wiki/Chiral_drugs

    In general the D/L system of nomenclature is superseded by the Cahn-Ingold-Prelog (CIP) rule to describe the configuration of a stereogenic/chiral center. In the CIP or R/S convention, or sequence rule, the configuration, spatial arrangements of ligands/substituents around a chiral center, is labeled as either "R" or "S".

  6. Axial chirality - Wikipedia

    en.wikipedia.org/wiki/Axial_chirality

    The designations are based on the same CahnIngoldPrelog 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]

  7. 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. ... CahnIngoldPrelog priority rules; F. Fajans' rules ...

  8. AOL Mail

    mail.aol.com

    Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

  9. 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]