One of the classical experiments in the development of olefin metathesis was the “double cross” metathesis in which a mixture of cyclooctene, 2-butene, and 4-octene underwent metathesis.
a. What products would be expected from this metathesis?
b. How would the formation of these products differ in the pairwise and non-pairwise mechanisms? (See T. J. Katz, J. McGinness, J. Am. Chem. Soc. , 1975 , 97 , 1592.)
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