Before: Toluene is refluxed with sodium-benzophenone to dry and deoxygenate it.After: The deep blue coloration of the benzophenone ketyl radical shows that the toluene to be distilled is dry and oxygen-free.
A ketyl group in organic chemistry is an anionradical that contains a group R2C−O•. It is the product of the 1-electron reduction of a ketone.
Another mesomeric structure has the radical position on carbon and the negative charge on oxygen.[1]
The ketyl radicals derived from the reaction of sodium and benzophenone is a common laboratory desiccant. Ketyls react quickly with the water, peroxides, and with oxygen. Thus, the deep purple coloration qualitatively indicates dry, peroxide-free, and oxygen-free conditions. The method for drying is still popular in many laboratories due to its ability to produce such pure solvent quickly. An alternative option for chemists interested only in water-free solvent is the use of molecular sieves. This is a much safer method than using an alkali metal still, produces solvent as dry as sodium-ketyl (though not as dry as potassium, or potassium-sodium alloy) but takes longer.[2]
Oxygen
Sodium benzophenone ketyl reacts with oxygen to give the sodium benzoate and sodium phenoxide.
Reducing agent
Potassium-benzophenone ketyl is used as a reductant for the preparation of organoiron compounds.[3]
^Williams, D. B. G., Lawton, M., "Drying of Organic Solvents: Quantitative Evaluation of the Efficiency of Several Desiccants", The Journal of Organic Chemistry 2010, vol. 75, 8351. doi:10.1021/jo101589h
^Plotkin, J. S.; Shore, S. G. (1981). "Convenient preparation and isolation of pure potassium cyclopentadienyldicarbonylferrate, K[(η5-C5H5)Fe(CO)2]". Inorg. Chem. 20: 284–285. doi:10.1021/ic50215a060.
