To study the mechanism of the sulfur vulcanization of rubber, 2,3-dimethyl-2-butene (C6H12) was used as a simple, low-molecular-weight model alkene. Only equivalent allylic positions are present in this alkene. Treating C6H12 with a mixture of ZnO, S8, and the accelerator tetramethylthiuramdisulfide at 140°C yields a mixture of addition products (C6H11—Sn—C6H11). RP-HPLC in combination with MS and 1H-NMR shows that the products differ only in the length of the sulfur bridge. Small quantities of isomerized products have been found, in which a 1,3-shift of the double bond has occurred.