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  Home > JCE Print > Journal of Chemical Education > Issues > 2000  > January  >
In the Classroom
Keep Going with Cyclooctatetraene!
Addison Ault
Department of Chemistry, Cornell College, Mount Vernon, IA 52314

Cover
January 2000
Vol. 77 No. 1
p. 55

Abstract
This paper shows how some simple properties of cyclooctatetraene can indicate important ideas about the structure of cyclooctatetraene. Its heat of hydrogenation indicates no significant stabilization by delocalization of electrons, and its alternating carbon-carbon bond lengths are consistent with the presence of alternating "ordinary" single and double bonds. The nonplanar nature of cyclooctatetraene is conclusively indicated by the diastereotopic nature of the methyl groups in its dimethylcarbinyl derivative, illustrating one way that NMR can reveal subtle details of molecular structure. Finally, the Diels-Alder reaction provides a simple but elegant illustration of how reaction mechanisms can be deduced.
More Information
*  Citation
Ault, Addison. J. Chem. Educ. 2000 77 55.
*  Keywords
Organic Chemistry; Aromaticity / Aromatics; NMR Spectrometry; Mechanisms; Pericyclic Reactions; Teaching / Learning Aids
*  History
Created:
Last Updated:
December 9, 1999
April 15, 2005
  Home > JCE Print > Journal of Chemical Education > Issues > 2000 > January > Page 55


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