The standard enthalpy of formation of \(\mathrm{H}_{2} \mathrm{O}(l)\) at \(298 \mathrm{~K}\) is \(-285.8\) \(\mathrm{kJ} / \mathrm{mol} .\) Calculate the change in internal energy for the following process at \(298 \mathrm{~K}\) and 1 atm: $$ \mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{H}_{2}(g)+\frac{1}{2} \mathrm{O}_{2}(g) \quad \Delta E^{\circ}=? $$ (Hint: Using the ideal gas equation, derive an expression for work in terms of \(n, R\), and \(T\).)

Short Answer

Expert verified
The change in internal energy for the given process at 298K and 1 atm is approximately -284.6 kJ/mol.

Step by step solution

01

From thermodynamics, we know that the change in enthalpy, \(\Delta H\), is related to the change in internal energy, \(\Delta E\), and the work done in a process, \(W\), as follows: $$ \Delta H = \Delta E + W $$ We want to find \(\Delta E\). So we need to calculate \(W\) and rearrange the equation: $$ \Delta E = \Delta H - W $$ #Step 2: Derive the work done using the ideal gas equation#

The ideal gas equation is given by: $$ PV=nRT $$ Where \(P\) is pressure, \(V\) is volume, \(n\) is the number of moles, \(R\) is the ideal gas constant, and \(T\) is the temperature. Now, let's consider the work done, \(W\), during the expansion of the gas. It can be expressed as: $$ W = -P\Delta V $$ Using the ideal gas equation, we can derive an expression for \(\Delta V\) in terms of \(n\), \(R\), and \(T\): $$ \Delta V = \frac{\Delta (nRT)}{P} $$ Substitute this expression back into the work equation: $$ W = -P \left(\frac{\Delta (nRT)}{P}\right) $$ Cancel out the pressure terms: $$ W = -\Delta(nRT) $$ #Step 3: Calculate the work done in the given process#
02

In the given process, we have the following stoichiometric changes in number of moles: $$ \Delta n = 1 + \frac{1}{2} - 1 = \frac{1}{2} $$ Now, we can substitute the values of \(\Delta n\), \(R\), and \(T\) into the work equation: $$ W = - \left(\frac{1}{2}\cdot 8.314 \ \mathrm{J/(mol\cdot K)} \cdot 298 \ \mathrm{K} \right) $$ Calculate the work done: $$ W \approx -1243 \ \mathrm{J/mol} $$ #Step 4: Calculate the change in internal energy#

Now that we have the work done, we can calculate the change in internal energy using the equation from Step 1: $$ \Delta E = \Delta H - W $$ Substitute the given values for \(\Delta H\) and the calculated value for \(W\): $$ \Delta E = -285.8 \ \mathrm{kJ/mol} - (-1243 \ \mathrm{J/mol}) $$ Convert the second term to kJ/mol: $$ \Delta E = -285.8 \ \mathrm{kJ/mol} + 1.243 \ \mathrm{kJ/mol} $$ Calculate the change in internal energy: $$ \Delta E \approx -284.6 \ \mathrm{kJ/mol} $$ Thus, the change in internal energy for the given process at 298K and 1 atm is approximately -284.6 kJ/mol.

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Most popular questions from this chapter

Combustion of table sugar produces \(\mathrm{CO}_{2}(g)\) and \(\mathrm{H}_{2} \mathrm{O}(l) .\) When \(1.46 \mathrm{~g}\) table sugar is combusted in a constant-volume (bomb) calorimeter, \(24.00 \mathrm{~kJ}\) of heat is liberated. a. Assuming that table sugar is pure sucrose, \(\mathrm{C}_{12} \mathrm{H}_{22} \mathrm{O}_{11}(s)\), write the balanced equation for the combustion reaction. b. Calculate \(\Delta E\) in \(\mathrm{kJ} / \mathrm{mol} \mathrm{C}_{12} \mathrm{H}_{22} \mathrm{O}_{11}\) for the combustion reaction of sucrose. c. Calculate \(\Delta I I\) in \(\mathrm{kJ} / \mathrm{mol} \mathrm{C}_{12} \mathrm{H}_{22} \mathrm{O}_{11}\) for the combustion reaction of sucrose at \(25^{\circ} \mathrm{C}\).

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