We report for the first time the performance of hybridized Cu/CaO-Al 2 O 3 catalysts for aqueous-phase hydrogenolysis of sorbitol to ethylene glycol (EG), 1,2-propanediol (1,2-PDO), and 1,2-butanediol (1,2-BDO) with linear alcohols as coproducts in a base-free liquid phase. These supported Cu catalysts with solid bases as promoters show significant activity for C−C cleavage and high selectivity (∼84%) to glycols and linear alcohols. The effects of Cu loading, catalyst pretreatment conditions, H 2 pressure, and temperature on activity and selectivity of Cu/CaO-Al 2 O 3 catalysts were investigated. The strong interaction between Cu and Ca 2+ cations in the solid support is found to facilitate C−C and C−O cleavage of sorbitol, as evidenced from TEM, SEM, and TPR studies of the catalysts. Surface characterization and activity tests further suggest that Ca x Cu y Al z O p (Phase I) promotes dehydrogenation and isomerization reactions, whereas spinal CuAl 2 O 4 (Phase II) species facilitates hydrogenation reactions. In addition, the overall activity and selectivity of the Cu catalysts may be easily tuned by the Cu/Ca 2+ molar ratio and catalyst preparation conditions. Cu/CaO-Al 2 O 3 catalysts also give higher overall yields of value-added glycols (63−82%) for facile conversion of various other sugar polyols such as glycerol (C 3 ), erythritol (C 4 ), xylitol (C 5 ), and mannitol (C 6 ) under similar reaction conditions. A surface reaction mechanism involving the formation of β-ketoses on multifunctional Cu−Ca 2+ sites is proposed.