The reaction mechanism of methylcyclopentane (MCP) ring opening on Rh catalysts (the participation of each intermediate in further hydrogenolysis vs. their desorption) was studied on a special series of Rh(Ge)/Al 2 O 3 catalysts. These were obtained by wet impregnation and adding different amounts of Ge by anchoring of Ge(n-C 4 H 9 ) 4 on the surface of Rh with preadsorbed hydrogen. As shown earlier [1], low amounts of Ge were deposited selectively on low-Miller-index microfacets, whereas excess use of Ge(n-C 4 H 9 ) 4 caused statistical deposition on Rh. This difference was also reflected in the ring-opening pattern: the sample with randomly located Ge behaved like the parent catalyst with dispersion of 80%. Each ring-opening intermediate hydrogenolyzed further nearly to the same extent; the ring opening product distribution (ROPD) showing thus no variation as a function of reaction conditions. The catalyst with selective Ge deposition followed, however, the pattern of a sintered sample: the surface intermediate of 2-methylpentane underwent preferential hydrogenolysis to smaller fragments. Thus, changing the position of Ge deposits (without modifying the particle size) induced changes in the prevailing reaction route.