This reaction is an example of the of an acid in an ionic liquid similar to the / discussed in lecture. This particular reaction has sorbic acid and hydrogen gas reacting with a ruthenium and a 1-butyl-3-methyl imidazolium hexafluorophosphate (bmimPF6)/methyl tert-butyl ether (MTBE) system to create cis-hex-3-enoic acid. The above reaction occurs with ~85% . The author of this paper was examining enantioselective hydrogenation in because this mechanism could provide a means for facile of of expensive . The author also studies some hydrogenation reactions that lead to the precursor of the antiinflammatory drug ibuprofen, the active ingredient in Advil.

The above reaction shows an epimeric steroid alcohol being converted by a catalyst of and to a of 17-estradiol 3-methyl ether and a . The racemic mixture is formed by converting the of the ether, where the hydroxyl group is on the top of the ring, to the of the ether, where the hydroxyl group is underneath the ring. The reaction is stopped when the amount of alpha ether is roughly equivalent to the amount of beta ether. In the notation used, the between the hydroxyl group and the ether shows that the hydroxyl group can be in either the front or the back of the .

However, a ketone can be produced instead of the alpha ether when the alcohol is oxidized. Because the purpose of the reaction is to racemize the ether, this ketone is an unwanted side product. To prevent oxidation, toluene at 100 C is used as a . The chemical properties of toluene slow the formation of the ketone so that at around 100 C, the yield of the racemic mixture is about 54%. Any ketone that does form can be separated from the ether by . This reaction is a good way to racemize the ether efficiently and inexpensively; it was traditionally synthesized at a much higher cost.