Selectivity, conversion, yield and kinetics of the liquid-phase dimerization of 2-methyl-1-butene and 2-methyl-2-butene mixture have been studied in a batch stirred tank reactor in the temperature range 60-100 degrees C catalysed by the acid resin Amberlyst 35 and using ethanol as a selectivity enhancer. Selectivity to dimers showed a maximum at R-IA/EtOH 20. Obtained diisoamylenes consisted mainly of 3,4,4,5-tetramethyl-2-hexene, 2,3,4,4-tetramethyl-1-hexene and 3,4,5,5-tetramethyl-2-hexene. LHHW type kinetic model was derived for the dimerization reaction as a whole. The kinetic model assumes that three active sites take part in the rate-limiting step of dimerization; the apparent activation energy for the dimerization reaction being 65 kJ mol(-1). A pseudohomogeneous kinetic model was used to describe the dimerization reaction network. The apparent activation energy for each dimerization reaction was found to be in the range 61-81 kJ mol(-1). (c) 2006 Elsevier Ltd. All rights reserved.