At certain temperatures, all metallic systems and their alloys melt from the solid state to liquid state – this transition temperature is known as the melting temperature of the corresponding system. This is simultaneously a critical and important phenomenon for all materials from metallurgical point of view. At this critical temperature, the structure of the system changes drastically from an ordered state to a disordered state. It is reiterated here that at the solid crystalline state of a metal, the atoms constitute a regular array maintaining both the short range and long range orders. However, after the melting temperature, the system retains only the short range order; the long range order smears out because of the breaking of the crystalline symmetry. In the vicinity of the melting, the system temporarily undergoes multi-phase transformations immediately before it goes to a homogeneous random state. At this state, the system becomes a homogeneous liquid. In the liquid state, structurally the system is characterized by two important functions, namely, the pair distribution function g(r) and the structure factor S(Q) – the latter being the Fourier transform of the earlier. In this project, we have initially investigated the temperature dependence of g(r) and S(Q) for 11 liquid metals: Sodium Na, Potassium K, Cesium Cs, Rubidium Rb, Zinc Zn, Cadmium Cd, Mercury Hg, Aluminum Al, Gallium Ga, Silicon Si and Germanium Ge, taken from different groups in the periodic table, at different temperatures. These were then followed by calculating the coordination numbers N i for v these systems at various temperatures. We have undertaken 3 methods in our project. Our plan follows the scheme: 1. Extraction of analytically patterns of g(r) and S(Q) from experiments: In this part, we extracted the graphical representation of g(r) and S(Q) from the results obtained from diffraction experiments of a number of metallic systems. This demonstrates the structural information of the systems in the vicinity of melting and beyond. 2. Theoretical deductions of g(r) and S(Q) : We have then theoretically deduced g(r) and S(Q) from the established equations of states. At this stage, temperature dependence of these functions has been precisely taken care of while calculating g(r) and S(Q) at various temperatures. These are found to be comparable to the experimental results just briefed. 3. Monte Carlo Simulation in calculating g(r) and S(Q): Our next effort was to compute g(r) and S(Q) by using the Monte Carlo Method of simulation at various temperatures. The results are observed to follow consistently both the experimental and theoretical trends. 4. Calculations of coordination numbers: Concurrently, we have calculated the coordination numbers (first, second and third) for 11 liquid metals mentioned earlier by using the experimentally extracted, theoretically calculated and simulated values for g(r), at various temperatures. The results for coordination numbers, Ni are found to be consistent with one another of the three methods undertaken. These values are observed to follow, to extent, a trend similar to their solid state counter parts.