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The suffixes -diol, -triol, -tetrol, etc., are used for multiple −OH groups: Ethylene glycol CH 2 OHCH 2 OH is ethane-1,2-diol. If higher precedence functional groups are present (see order of precedence, below), the prefix "hydroxy" is used with the bonding position: CH 3 CHOHCOOH is 2-hydroxypropanoic acid.
Numerical prefixes for multiplication of compound or complex (as in complicated) features are created by adding kis to the basic numerical prefix, with the exception of numbers 2 and 3, which are bis- and tris-, respectively.
In Latin and Greek, the ordinal forms are also used for fractions for amounts higher than 2; only the fraction 1 / 2 has special forms. The same suffix may be used with more than one category of number, as for example the orginary numbers second ary and terti ary and the distributive numbers bi nary and ter nary .
The use of the prefixes ortho, meta and para to distinguish isomers of disubstituted aromatic rings starts with Wilhelm Körner in 1867, although he applied the ortho prefix to a 1,4-isomer and the meta prefix to a 1,2-isomer.
Pentan-2-one or 2-pentanone pentan-3-one or 3-pentanone The International Union of Pure and Applied Chemistry (IUPAC) recommends the use of numeric prefixes to indicate the position of substituents, generally by identifying the parent hydrocarbon chain and assigning the carbon atoms based on their substituents in order of precedence .
See: E-Z notation Violet leaf aldehyde, systematic name (E,Z)-nona-2,6-dienal, is a compound having one (E)- and one (Z)-configured double bond. 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.
The Greek series proto-, deutero-, trito-, ... is only found in prefixes, generally scholarly and technical coinages, e.g. protagonist, deuteragonist, tritagonist; protium, deuterium, tritium; Proto-Isaiah, Deutero-Isaiah. [3] Numbers beyond three are rare; those beyond four are obscure. The first twelve variations of ordinal numbers are given ...
Another nomenclature uses the systematic name of the molecular graph, a ' D-' or ' L-' prefix to indicate the position of the last chiral hydroxyl on the Fischer diagram (as above), and another italic prefix to indicate the positions of the remaining hydroxyls relative to the first one, read from bottom to top in the diagram, skipping the keto ...