Calculate the enthalpy of the reaction \(\mathrm{P}_{4}(\mathrm{~s})+10 \mathrm{Cl}_{2}(\mathrm{~g}) \rightarrow 4 \mathrm{PCl}_{5}(\mathrm{~s})\) from the reactions $$ \begin{gathered} \mathrm{P}_{4}(\mathrm{~s})+6 \mathrm{Cl}_{2}(\mathrm{~g}) \longrightarrow 4 \mathrm{PCl}_{3}(\mathrm{I}) \\ \Delta H^{\circ}=-1278.8 \mathrm{~kJ} \\ \mathrm{PCl}_{3}(\mathrm{l})+\mathrm{Cl}_{2}(\mathrm{~g}) \longrightarrow \mathrm{PCl}_{5}(\mathrm{~s}) \\ \Delta H^{m}=-124 \mathrm{~kJ} \end{gathered} $$

Chemical thermodynamics studies the relationship between heat, work, and chemical reactions or with the physical changes of state that classify them. It is a bridge connecting thermodynamics and chemistry and is essential for understanding energy changes in chemical systems. Enthalpy, represented as \(H\), is a fundamental concept here; it describes the total heat content of a system at constant pressure.

The first law of thermodynamics, also known as the law of energy conservation, states that energy cannot be created or destroyed, only transformed. In chemical reactions, this principle is observed through the changes in enthalpy, where the heat released or absorbed can be calculated using the reaction's stoichiometry and the enthalpies of individual reactions. By considering the entropic and enthalpic factors, chemical thermodynamics allows us to predict whether a process will occur spontaneously. It is key in designing chemical reactions that are favorable from both an energetic and practical standpoint.

The enthalpy of reaction, commonly denoted as \(\Delta H\), is a measure of the heat change during a chemical reaction carried out at constant pressure. It is either absorbed or evolved, indicating endothermic or exothermic reactions, respectively. When presented with stepwise reactions, like the formation of PCl5 from P4 and Cl2, the Hess's law comes into play. According to Hess's law, the total enthalpy change in a chemical reaction is the same, no matter how the reaction occurs, as long as the initial and final states are the same.

Hence, by algebraically summing up the enthalpy changes (\(\Delta H\)) for each step provided, we can find the overall \(\Delta H\) for the reaction of interest. This principle is critical in calculating the enthalpy change for reactions where the direct method may be impracticable. By capturing the calorimetric data from related reactions, like those given in the exercise, and applying Hess's law, we deduce the enthalpy change for complex reactions.

Stoichiometry is the quantitative study of reactants and products in a chemical reaction. It allows chemists to predict the amounts of substances consumed and produced in a given reaction based on the reaction coefficients indicated in the balanced chemical equation.

In practical terms, stoichiometry can tell us how much product we can expect from a certain amount of reactants, which is invaluable in both laboratory and industrial chemical synthesis. When calculating enthalpy changes, stoichiometry plays a pivotal role. For the accurate determination of enthalpy change, we utilize the stoichiometric coefficients to adjust the known enthalpies of formation or reaction. This is exemplified in the step by step solution where the known reactions are multiplied by their respective stoichiometric coefficients to align with the target reaction. This allows for precise cancelation of intermediates and provides the correct enthalpy change associated with the final balanced equation for the chemical process under investigation.