According to the current version of Nomenclature of Organic Chemistry – IUPAC Recommendations and Preferred Names 2013 (Blue Book), a structure with two or more identical units that are linked by di- or polyvalent groups can be named in two ways:
- by ordinary substitutive nomenclature, in which one of the parent structures is chosen as the senior parent structure and the remainder of the structure is expressed by substituent prefixes
- by multiplicative nomenclature, in which two or more parent structures are connected by symmetrical or unsymmetrical single or concatenated substituent groups
Both methods yield correct names, which may be used in general nomenclature. However, the IUPAC recommendations define a preferred IUPAC name (PIN), which is the name preferred among two or more names generated from two or more IUPAC recommendations.
P-45.1 MULTIPLICATION OF IDENTICAL SENIOR PARENT STRUCTURES
P-45.1.1 Multiplicative nomenclature is senior to substitutive nomenclature for generating preferred IUPAC names to express multiple occurrences of identical senior parent structures, other than alkanes, in the name of the parent structure (see P-51.3.1). In most cases multiplicative names are shorter than regular substitutive names. A preferred IUPAC name is generated by multiplicative nomenclature when the following criteria for its use are met (see P-51.2.3).
(1) the linking bonds (single or multiple) between the central substituent group of the multiplicative group and all subsequent structural units are identical; and
(2) the multiplicative groups, other than the central multiplicative group, are symmetrically substituted; and
(3) the locants of all substituent groups on the identical parent structures, including suffix groups, are identical.
When these conditions are not met, substitutive nomenclature generates preferred IUPAC names.
The given structure of the DDT molecule fulfils these requirements; therefore, the preferred IUPAC name is generated by multiplicative nomenclature as follows.
P-220.127.116.11 Multiplicative name formation
Multiplicative names are formed in accordance with the number of occurrences of identical structural units as defined in P-18.104.22.168 and the relationship of the linking multiplicative substituent group to the identical structural units.
When a compound contains identical structural units as defined in P-22.214.171.124 linked by a symmetrical simple, compound, complex, or concatenated multiplicative group (a di- or polyvalent substituent group), it is named by stating successively:
(a) the locants for the positions of substitution of the linking multiplicative substituent atom or group to the identical parent structural unit (the locant 1 is omitted when alone in the name of a mononuclear parent hydride);
(b) the name of the linking multiplicative substituent atom or group;
(c) the numerical prefix ‘di’, ‘tri’, etc.; and/or ‘bis-‘, ‘tris-‘, etc., with no elision of the final vowel before the name of the identical parent structural unit;
(d) the name of one of the identical structural units including the principal characteristic group and substituents, if any, enclosed in appropriate enclosing marks (see P-16.5).
The numbering of the identical parent structural unit is retained and, when there is a choice, the locants of the point of substitution by the linking multiplicative substituent groups on the identical parent structure are as low as possible.
Here: 1,1'-(…)bis(4-chlorobenzene) (not 4,4'-(…)bis(1-chlorobenzene))
Therefore, the preferred IUPAC name is 1,1'-(2,2,2-trichloroethane-1,1-diyl)bis(4-chlorobenzene)