Bring the power of IUPAC naming to your desktop!

ACD/Name (Chemist Version) offers a standardized set of features for quick and simple generation of IUPAC names, and structures from names. It is a streamlined version of our popular ACD/Name software.

View a full description and pricing on our web store.

Nomenclature Systems

C-0.0 General Principles

(1) The various classes of compound are dealt with in detail in the later Subsections C-l to C-9. The following is a summary of general principles.

(2) The formation of a name for a chemical compound usually involves the following steps, to be taken so far as they are applicable in the order given:

(a) From the nature of the compound determine the type of nomenclature to be used (substitutive, radicofunctional, additive, subtractive, conjunctive or replacement); or treat as an assembly of identical units.

(b) Determine the kind of characteristic group for use as the principal group, if any. Only one kind of characteristic group should be cited as suffix or functional class name. All substituents not so cited must be named as prefixes.

(c) Determine the parent structure (principal chain, parent ring system, or conjunctive components).

(d) Name the parent structure and the principal group(s).

(i) Determine and name the infixes and prefixes

(f) Complete the numbering.

(g) Assemble the partial names into a complete name, using for all the detachable prefixes the alphabetical order.

(3) Details for each of the above steps and for each type of nomenclature are given in the rules which follow.

(4) In substitutive nomenclature some characteristic groups can be denoted either as prefixes or as suffixes, but others only as prefixes. Radicofunctional nomenclature differs in that separate words (or in some languages suffixes) designating the principal group(s) are associated with radical names designating the remainder of the structure. The characteristic groups that can be cited as suffixes in substitutive nomenclature are not necessarily identical with the groups designated by the functional class name when radicofunctional nomenclature is used (e.g., butanone and ethyl methyl ketone, where -one denotes =O and ketone denotes >CO).

See Recommendations'93 R-4, Tables 5, 9 and 10

See also:

Substitutive nomenclature

Radicofunctional nomenclature

Additive nomenclature

Subtractive nomenclature

Conjuctive nomenclature

Replacement nomenclature

Nomenclature of assemblies of identical units

Free radicals, ions, and radical ions


search
This HTML reproduction of Sections A, B and C of IUPAC "Blue Book" is as close as possible to the published version [see Nomenclature of Organic Chemistry, Sections A, B, C, D, E, F, and H, Pergamon Press, Oxford, 1979. Copyright 1979 IUPAC.] If you need to cite these rules please quote this reference as their source.

Published with permission of the IUPAC by Advanced Chemistry Development, Inc., www.acdlabs.com, +1(416)368-3435 tel, +1(416)368-5596 fax. For comments or suggestions please contact webmaster@acdlabs.com