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Curtin–Hammett principle

In a chemical reaction that yields one product (X) from one conformational isomer (A') and a different product (Y) from another conformational isomer (A'') (and provided these two isomers are rapidly interconvertible relative to the rate of product formation, whereas the products do not undergo interconversion) the product composition is not in direct proportion to the relative concentrations of the conformational isomers in the substrate ; it is controlled only by the difference in standard free energies (δ Δ ‡ G) of the respective transition states.
It is also true that the product composition is formally related to the relative concentrations of the conformational isomers A' and A'' (i.e. the conformational equilibrium constant) and the respective rate constants of their reactions; these parameters are generally — though not invariably — unknown. The diagram below represents the energetic situation for transformation of interconverting isomers A and A' into products X and Y.
PAC, 1994, 66, 1077 (Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994)) on page 1102
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IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic, J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8. doi:10.1351/goldbook.
Last update: 2014-02-24; version: 2.3.3.
DOI of this term: doi:10.1351/goldbook.C01480.
Original PDF version: http://www.iupac.org/goldbook/C01480.pdf. The PDF version is out of date and is provided for reference purposes only. For some entries, the PDF version may be unavailable.
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