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  Home > JCE Print > Journal of Chemical Education > Issues > 2001  > July  >
In the Classroom
The Bullvalene Story. The Conception of Bullvalene, a Molecule That Has No Permanent Structure
Addison Ault
Department of Chemistry, Cornell College, Mount Vernon, IA 52314

Cover
July 2001
Vol. 78 No. 7
p. 924

Abstract
In this paper I review and summarize the logical process through which Doering and Roth (Tetrahedron 1963, 19, 715) conceived of the possible existence of an isomer of molecular formula C10H10 that has a "fluxional" structure. That is, the molecule has a structure in which every carbon atom is equally bonded, or not bonded, to every other carbon. The evidence for its "fluxional" structure is that it gives a sharp singlet in its proton NMR spectrum. In order for the 10 protons, each bonded to a carbon atom, to be chemical-shift equivalent, Doering and Roth conclude that "all ten carbon atoms [must] inevitably wander over the surface of a sphere in ever changing relationship to each other."
More Information
*  Citation
Ault, Addison. J. Chem. Educ. 2001 78 924.
*  Keywords
History / Philosophy; Molecular Properties / Structure; Organic Chemistry
*  History
Created:
Last Updated:
June 6, 2001
August 31, 2005
  Home > JCE Print > Journal of Chemical Education > Issues > 2001 > July > Page 924


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