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Descriptor (chemistry)

type of notational prefix in chemistry nomenclature

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Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionAug 9, 2026
Entity authorityQ1200761 ↗
Source-derived summary

In chemical nomenclature, a descriptor is a notational prefix placed before the systematic substance name, which describes the configuration or the stereochemistry of the molecule. Some of the listed descriptors should not be used in publications, as they no longer accurately correspond with the recommendations of the IUPAC. Stereodescriptors are often used in combination with locants to clearly identify a chemical structure unambiguously.

The descriptors, usually placed at the beginning of the systematic name, are not taken into account in the alphabetical sorting.

Configuration descriptors

cis, trans

See: cis–trans isomerism

The descriptors cis (Latin, on this side of) and trans (Latin, over, beyond) are used in various contexts for the description of chemical configurations:

In organic structural chemistry, the configuration of a double bond can be described with cis and trans, in case it has a simple substitution pattern with only two residues. The position of two residues relative to one another at different points in a ring system or a larger molecule can also be described with cis and trans if the structure's configuration is rigid and does not allow simple inversion.

In inorganic complex chemistry, the descriptors cis and trans are used to characterize the positional isomers in octahedral complexes with A2B4X configuration or square planar complexes with A2B2X configuration.

The typographic presentation of cis and trans is italicised and in lower case letters.

The cis/trans nomenclature is not unambiguous for more highly substituted double bonds and is nowadays largely replaced by the (E)/(Z) nomenclature.

(E), (Z)

See: E-Z notation

The descriptors (E) (from German entgegen, 'opposite') and (Z) (from German zusammen, 'together') are used to provide a distinct description of the substitution pattern for alkenes, cumulenes or other double bond systems such as oximes.

For the attribution of (E) or (Z) is based on the relative position of the two substituents of highest priority are on each side of the double bond, while the priority is based on the Cahn–Ingold–Prelog (CIP) nomenclature.

Editorial summary

The public source identifies “Descriptor (chemistry)” as type of notational prefix in chemistry nomenclature. This brief keeps that definition visible, then builds a research path around Descriptor, chemistry and type.

Editorial reviewA concise reference frame for defining the subject, testing terminology and identifying the institution closest to the evidence. The current 325-word lead offers orientation but no explicit four-digit date, so chronology should not be assumed. The selected authority fields contribute no independent date. Its value is orientation rather than verdict, with Descriptor, chemistry and type providing the first useful test.
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The citation trail is more important than the brevity of the summary: it shows where individual claims can be examined in context. The source revision retrieved here is dated Aug 9, 2026. The linked authority identifier is Q1200761. None of the 0 selected statements returned an explicit reference.

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Source & attribution

This entry incorporates text from “Descriptor (chemistry)” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.