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The standard enthalpy of reaction (denoted ) for a chemical reaction is the difference between total product and total reactant molar enthalpies, calculated for substances in their standard states. The value can be approximately interpreted in terms of the total of the chemical bond energies for bonds broken and bonds formed.
For many substances, the formation reaction may be considered as the sum of a number of simpler reactions, either real or fictitious. The enthalpy of reaction can then be analyzed by applying Hess' law, which states that the sum of the enthalpy changes for a number of individual reaction steps equals the enthalpy change of the overall reaction.
Since enthalpy is a state function, the given for a particular reaction is only true for that exact reaction. Physical states of reactants and products matter, as do molar concentrations. Physical states of reactants and products matter, as do molar concentrations.
Enthalpy is an extensive property; it is proportional to the size of the system (for homogeneous systems). As intensive properties, the specific enthalpy, h = H / m , is referenced to a unit of mass m of the system, and the molar enthalpy, H m = H / n , where n is the number of moles.
Enthalpy of mixing can often be ignored in calculations for mixtures where other heat terms exist, or in cases where the mixture is ideal. [2] The sign convention is the same as for enthalpy of reaction: when the enthalpy of mixing is positive, mixing is endothermic, while negative enthalpy of mixing signifies exothermic mixing. In ideal ...
The Van 't Hoff equation relates the change in the equilibrium constant, K eq, of a chemical reaction to the change in temperature, T, given the standard enthalpy change, Δ r H ⊖, for the process. The subscript r {\displaystyle r} means "reaction" and the superscript ⊖ {\displaystyle \ominus } means "standard".
That is, the heat of combustion, ΔH° comb, is the heat of reaction of the following process: C c H h N n O o (std.) + (c + h ⁄ 4 - o ⁄ 2) O 2 (g) → c CO 2 (g) + h ⁄ 2 H 2 O (l) + n ⁄ 2 N 2 (g) Chlorine and sulfur are not quite standardized; they are usually assumed to convert to hydrogen chloride gas and SO 2 or SO
The integral heat of dissolution is defined as a process of obtaining a certain amount of solution with a final concentration. The enthalpy change in this process, normalized by the mole number of solute, is evaluated as the molar integral heat of dissolution. Mathematically, the molar integral heat of dissolution is denoted as: