The speciation of Sn(IV)-Br− and Sn(II)-Cl− in concentrated Br− and Cl− media were investigated by cyclic voltammetry, which is the continuous study from the previously reported Sn(II)-Br− speciation Park and Chang (2016) . We first determined the speciation of Sn(IV)-Br− in concentrated Br− acidic aqueous solutions with ionic strength of 6. SnBrj4−j complexes with 1≤j≤5 and their corresponding fractional diagrams were determined based on their estimated stability constants, βjSn(IV)−Br−. In acidic aqueous solutions where the concentration of Br− was less than 2M, both SnBr3+ and SnBr22+ were estimated to be the main Sn(IV)-Br− species. Meanwhile, as the Br− concentration increased >2M, the fraction of SnBr5− was significantly increased and became the main species among Sn(IV)-Br− complexes. For the Sn(II)-Cl− speciation, SnClk2−k complexes with 1≤k≤7 were determined as the concentration of Cl− increased to 6M in acidic aqueous solutions. The fractional diagrams of SnClk2−k complexes were obtained from the estimated βkSn(II)−Cl−. Based on the fractions of Sn(II)-Cl− species, SnCl+ was the main species as the concentration of Cl− was less than 1M. As the Cl− concentration increased from 1 to 6M, SnCl75− became dominant among Sn(II)-Cl− complexes. We tried to determine the speciation of Sn(IV)-Cl− by cyclic voltammetry. However, the determination of Sn(IV)-Cl− speciation was experimentally limited because of the potential inversion of electrochemical reduction between Sn(IV)-Cl−/Sn(II)-Cl− and Sn(II)-Cl−/Sn.