This is the first time a microscopic theory-based bottom-up approach has been implemented to derive an analytical expression for the solvation energy for a finite (N) system, including the bulk. This bottom-up approach provides the information on solvation energies of anionic solutes in finite-size clusters, including the bulk (N = ∞), from the knowledge of the detachment energies for the system containing a few numbers of solvent molecules. However, in the case of dielectric constant, a microscopic theory-based top-down approach has been prescribed to derive an analytical expression for the static dielectric constant for the finite system. In this approach, the knowledge of the dielectric constant for the bulk provides a scheme to obtain the same quantity for a wide numbers of solvent molecules. As an illustrative example, the hydrated doubly charged anions, SO−2 4 .NH2O and C2 O−24 .NH2O, have been considered, and the calculated bulk solvation energy for the SO−24 .NH2O system is found to be in very good agreement (within 5%) with the available experimental result. However, the same quantity calculated based on the Born model is found to be largely deviating (32%) from the experimental result. The calculated results of the dielectric constant for these two systems support the linear theory of dielectric constant.