Publication Date
January 2000
Abstract
Epoxides, or oxiranes, are among the most versatile intermediates in organic synthesis. Yet very few examples of laboratory experiments involving reactions of epoxides are to be found in lab texts. We have developed a discovery-oriented laboratory experiment that involves the rearrangement of both cis- and trans-stilbene oxides with boron trifluoride etherate. The identity of the product can be easily determined by 1H NMR spectroscopy and, in case of the trans isomer, by preparation of the semicarbazone derivative as well. In spite of the simplicity of the experiment, the element of discovery ensures that student interest and enthusiasm are retained.
Disciplines
Organic Chemistry
Recommended Citation
Mohan, Ram; Sgariglia, Erik; Schopp, Regina; and Gavardinas, Kostas, "The Discovery-Oriented Approach to Organic Chemistry. 3. Boron-trifluoride Catalyzed Rearrangement of cis- and trans-Stilbene Oxides. An Exercise in 1H NMR Spectroscopy for Sophomore Organic Laboratories" (2000). Scholarship. 41.
https://digitalcommons.iwu.edu/chem_scholarship/41