The temperature in K at which \(\Delta G = 0\), for a given reaction with \(\Delta H = -20.5 \text{ kJ mol}^{-1}\) and \(\Delta S = -50.0 \text{ J K}^{-1} \text{ mol}^{-1}\) is:
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Always double-check your unit scales! Mixing \(\text{kJ}\) and \(\text{J}\) is a classic trap. Notice that if you forgot to multiply by \(1000\), you would evaluate \(\frac{-20.5}{-50} = 0.41\), or if you inverted the fraction, you would get \(2.44\) (matching choice 3). Keeping track of your unit multipliers keeps these calculation slip-ups at bay.
Concept:
The spontaneity of a chemical process is governed by the Gibbs-Helmholtz Equation, which relates change in Gibbs free energy (\(\Delta G\)), change in enthalpy (\(\Delta H\)), and change in entropy (\(\Delta S\)) at a constant thermodynamic absolute temperature (\(T\)):
\[
\Delta G = \Delta H - T\Delta S
\]
When a system reaches dynamic equilibrium, the net change in Gibbs free energy is exactly zero (\(\Delta G = 0\)). Setting this condition allows us to solve for the specific threshold temperature:
\[
0 = \Delta H - T\Delta S \quad \Rightarrow \quad T = \frac{\Delta H}{\Delta S}
\]
Critical Requirement: The units for both thermodynamic energy variables must match before division (usually by transforming kilojoules into joules via \(1 \text{ kJ} = 1000 \text{ J}\)).
Step 1: Convert the given values to matching metric units.
We are given the following parameters:
• Enthalpy change (\(\Delta H\)) \(= -20.5 \text{ kJ mol}^{-1} = -20.5 \times 1000 \text{ J mol}^{-1} = -20500 \text{ J mol}^{-1}\)
• Entropy change (\(\Delta S\)) \(= -50.0 \text{ J K}^{-1} \text{ mol}^{-1}\)
Step 2: Substitute parameters into the equilibrium temperature formula.
Using the derived relation \(T = \frac{\Delta H}{\Delta S}\):
\[
T = \frac{-20500 \text{ J mol}^{-1}}{-50.0 \text{ J K}^{-1} \text{ mol}^{-1}}
\]
Cancel out the negative signs in both the numerator and denominator:
\[
T = \frac{20500}{50}
\]
\[
T = 410 \text{ K}
\]