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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. File:CIP system example.svg - Wikipedia

    en.wikipedia.org/wiki/File:CIP_system_example.svg

    Cahn-Ingold-Prelog-prioriteitsregels; Usage on pt.wikipedia.org Regras de Cahn-Ingold-Prelog; Usage on ro.wikipedia.org Regulile Cahn-Ingold-Prelog; Usage on ru.wikipedia.org Правила Кана — Ингольда — Прелога; Usage on sh.wikipedia.org Kan-Ingold-Prelog pravila; Usage on sk.wikipedia.org Cahnov-Ingoldov-Prelogov R ...

  5. Category:Eponymous chemical rules - Wikipedia

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

    Download QR code; Print/export Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... CahnIngoldPrelog priority rules; F. Fajans ...

  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. 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.

  8. 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.

  9. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    The R/S system is assigned to a molecule based on the priority rules assigned by CahnIngoldPrelog priority rules, in which the group or atom with the largest atomic number is assigned the highest priority and the group or atom with the smallest atomic number is assigned the lowest priority.