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R-7.1.2 The E/Z Convention In names of compounds, steric relationships around one or more double bonds can be designated by the stereodescriptors Z and/or E
, assigned as follows. The sequence-rule-preferred atom or group (see R-7.2.1) attached to one of a doubly bonded pair of atoms is compared with the sequence-rule-preferred
atom or group attached to the other of that doubly bonded pair of atoms; if the selected atoms are on the same side of the reference plane (see R-7.1.1) the italic capital letter
Z is used as the stereodescriptor; if the selected atoms are on opposite sides, the italic capital letter E is used as the stereodescriptor. These stereodescriptors, placed in
parentheses followed by a hyphen, normally precede the whole name; if the molecule contains several double bonds, then each stereodescriptor is immediately preceded by the lower or less primed locant
of the relevant double bond.
Examples to R-7.1.2
This HTML reproduction is as close as possible to the published version [see IUPAC, Commission on Nomenclature of Organic Chemistry. A Guide to IUPAC Nomenclature of Organic Compounds
(Recommendations 1993), 1993, Blackwell Scientific publications, Copyright 1993 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 firstname.lastname@example.org