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  Home > JCE Print > Journal of Chemical Education > Issues > 2002  > April  >
In the Laboratory
Keto-Enol Tautomers in a Carbonyl Phosphonium Salt
David E. Berry and G. W. Patenaude
Department of Chemistry, University of Victoria, Victoria, BC V8W 3V6, Canada
Cover
April 2002
Vol. 79 No. 4
p. 498
Abstract
Supplementary NMR data is provided for an experiment previously published in this Journal describing the synthesis of carbonyl-stabilized ylides. The new data suggest that the keto-enol tautomerism is taking place in the phosphonium ion.
More Information
*  Citation
 Berry, David E.; Patenaude, G. W. J. Chem. Educ. 2002 79 498.
*  Keywords
 Inorganic Chemistry; Inorganic Synthesis; Laboratory Instruction; NMR Spectrometry; Organometallics; Phosphorus
*  History
 Created:
Last Updated:		 March 1, 2002
March 16, 2005
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