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(8) s-Indacene
(7) as-Indacene
(10) Fluorene
(9) Acenaphthylene
(12) Phenanthrene
(11) Phenalene
(13) Anthracene
(14) Fluoranthene
(18) Pyrene
(17) Triphenylene
(19) Chrysene
(20) Naphthacene
(21) Pleiadene
(22) Picene
(23) Perylene
(24) Pentaphene
(25) Pentacene
(26) Tetraphenylene
(27) Hexaphene
(28) Hexacene
(29) Rubicene
(30) Coronene
(31) Trinaphthylene
(32) Heptaphene
(33) Heptacene
(34) Pyranthrene
(35) Ovalene
21.2 - The names of hydrocarbons containing five or more fused benzene rings in a
straight linear arrangement are formed from a numerical prefix as specified in Rule A-1.1
followedby "-acene".
21.4 - The prefixes designating attached components are formed by changing the ending
"-ene" of the name of the component hydrocarbon into "-eno"; e.g., "pyreno" (from
pyrene). When more than one prefix is present, they are arranged in alphabetical order.
The following common abbreviated prefixes are recognized (see list in Part.1 of this
rule):
21.6 - When a name applies equally to two or more isomeric condensed parent ring
systems with the maximum number of non-cumulative double bonds and when the name
can be made specific by indicating the position of one or more hydrogen atoms in the
structure, this is accomplished by modifying the name with a locant, followed by italic
capital H for each of these hydrogen atoms. Such symbols ordinarily precede the name.
The said atom or atoms are called "indicated hydrogen". The same principle is applied to
radicals and compounds derived from these systems.
Next:
Numbering
Hydrogenated Compounds
Radical Names from Trivial and Semi-trivial Names
Radical Names for Fused Cyclic Systems with Side Chains
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.
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