The standard enthalpy and standard entropy changes for the oxidation of ammonia at 298 K are –382.64 kJ mol–1 and –145.6 JK–1 mol–1, respectively. Standard Gibbs energy change for the same reaction at 298 K is
–339.3 kJ mol–1
– 439.3 kJ mol–1
–523.2 kJ mol–1
–221.1 kJ mol–1
To find the standard Gibbs energy change \((\Delta G^\circ)\) for the oxidation of ammonia at 298 K, we can use the Gibbs free energy equation:
\(\Delta G^\circ = \Delta H^\circ - T\Delta S^\circ\)
where:
Given values:
Note that \(\Delta S^\circ\) must be converted to kJ K-1 mol-1 to match the units of \(\Delta H^\circ\). This conversion is done by dividing by 1000:
\(\Delta S^\circ = -145.6 \text{ J K}^{-1} \text{ mol}^{-1} = -0.1456 \text{ kJ K}^{-1} \text{ mol}^{-1}\)
Now substitute the values into the Gibbs free energy equation:
\(\Delta G^\circ = (-382.64 \text{ kJ mol}^{-1}) - (298 \text{ K})(-0.1456 \text{ kJ K}^{-1} \text{ mol}^{-1})\)
Calculate the temperature-entropy product:
\(T\Delta S^\circ = (298 \text{ K})(-0.1456 \text{ kJ K}^{-1} \text{ mol}^{-1}) = -43.3888 \text{ kJ mol}^{-1}\)
Substitute this back into the equation:
\(\Delta G^\circ = -382.64 \text{ kJ mol}^{-1} + 43.3888 \text{ kJ mol}^{-1}\)
Simplify the equation:
\(\Delta G^\circ = -339.2512 \text{ kJ mol}^{-1}\)
Rounding to match the precision of the given options, we obtain:
\(\Delta G^\circ \approx -339.3 \text{ kJ mol}^{-1}\)
Thus, the correct answer is -339.3 kJ mol-1.
A real gas within a closed chamber at \( 27^\circ \text{C} \) undergoes the cyclic process as shown in the figure. The gas obeys the equation \( PV^3 = RT \) for the path A to B. The net work done in the complete cycle is (assuming \( R = 8 \, \text{J/molK} \)):
