A
molecular rearrangement in which the principal product is indistinguishable (in the absence of
isotopic labelling) from the principal reactant. The term includes both '
degenerate intramolecular rearrangements' and reactions that involve
intermolecular transfer of atoms or groups ('
degenerate intermolecular rearrangements'): both are degenerate
isomerizations. The occurrence of degenerate rearrangements may be detectable by
isotopic labelling or by dynamic NMR techniques. For example: the [3,3]
sigmatropic rearrangement of hexa-1,5-diene (Cope
rearrangement):
Synonymous but less preferable terms are '
automerization', '
permutational isomerism', '
isodynamic transformation', '
topomerization'.
Source:
PAC, 1994, 66, 1077
(Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994))
on page 1104
InChI=1/C6H10/c1-3-5-6-4-2/h3-4H,1-2,5-6H2
InChI=1/C6H10/c1-3-5-6-4-2/h3-4H,1-2,5-6H2
PYGSKMBEVAICCR-UHFFFAOYAB
PYGSKMBEVAICCR-UHFFFAOYAB
Cite as:
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.
https://doi.org/10.1351/goldbook.