Extraction of individual organic sulfur compounds with anhydrous liquid hydrogen fluoride shows an orderly progression with changes in sulfur type, in molecular weight, or in configuration of substituent groups. Increased extraction is obtained in going from mercaptans to disulfides to thio ethers, but extraction is decreased with increasing molecular weight of a given type of sulfur compound. Whereas transition from primary to secondary to tertiary alkyl substituents results in progressively increased extraction, introduction of the phenyl group markedly lowers extraction. These relations are in keeping with the Lewis acid-base concept and with fundamental principles of electronegativity as related to structure.