For a particular reaction, \(\Delta H=-32 \mathrm{kJ}\) and \(\Delta S=-98 \mathrm{J} / \mathrm{K}\) . Assume that \(\Delta H\) and \(\Delta S\) do not vary with temperature. (a) At what temperature will the reaction have \(\Delta G=0\) ? (b) If \(T\) is increased from that in part (a), will the reaction be spontaneous or nonspontaneous?

Short Answer

Expert verified
(a) The temperature at which the reaction will have \(\Delta G = 0\) is approximately \(T \approx 326.53\,\text{K}\). (b) As the temperature increases from \(T \approx 326.53\,\text{K}\), the reaction will become nonspontaneous.

Step by step solution

01

Set up the equation for the Gibbs free energy change

We have the equation for Gibbs free energy change: \[ \Delta G = \Delta H - T\Delta S \] We're given \(\Delta H = -32\,\text{kJ}\) and \(\Delta S = -98\,\text{J/K}\). Note that we must convert \(\Delta H\) to J so that the units are consistent in the equation: \(-32\,\text{kJ} = -32,000\,\text{J}\). Now we can write the equation with the given values: \[ \Delta G = -32,000\,\text{J} - T(-98\,\text{J/K}) \]
02

Solve for the temperature at which \(\Delta G = 0\)

We want to find the temperature \(T\) at which the free energy change \(\Delta G = 0\). Thus, we can set the equation to zero and solve for \(T\): \[ 0 = -32,000\,\text{J} + 98\,\text{J/K} \cdot T \] Now, isolate the temperature on one side of the equation: \[ T = \frac{32{,}000\,\text{J}}{98\,\text{J/K}} \] Divide to find the temperature: \[ T \approx 326.53\,\text{K} \]
03

Determine if the reaction is spontaneous or nonspontaneous when the temperature increases

To find if the reaction is spontaneous or nonspontaneous, we must first look at the sign of \(\Delta G\) as the temperature increases. Recall that for this problem, both \(\Delta H\) and \(\Delta S\) are negative. When the temperature increases from \(T \approx 326.53\,\text{K}\), the magnitude of the term \(T\Delta S\) will also increase, because the product of two negative numbers will be positive. Since \(\Delta H\) is already negative, adding more positive values (increasing the magnitude of \(T\Delta S\)) will make \(\Delta G\) more positive. When \(\Delta G\) is positive, the reaction is nonspontaneous. In summary, as the temperature increases from \(T \approx 326.53\,\text{K}\), the reaction will become nonspontaneous.

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Most popular questions from this chapter

A standard air conditioner involves a refrigerant that is typically now a fluorinated hydrocarbon, such as \(\mathrm{CH}_{2} \mathrm{F}_{2} .\) An air- conditioner refrigerant has the property that it readily vaporizes at atmospheric pressure and is easily compressed to its liquid phase under increased pressure. The operation of an air conditioner can be thought of as a closed system made up of the refrigerant going through the two stages shown here (the air circulation is not shown in this diagram). During expansion, the liquid refrigerant is released into an expansion chamber at low pressure, where it vaporizes. The vapor then undergoes compression at high pressure back to its liquid phase in a compression chamber. (a) What is the sign of \(q\) for the expansion? (b) What is the sign of q for the compression? (c) In a central air-conditioning system, one chamber is inside the home and the other is outside. Which chamber is where, and why? (d) Imagine that a sample of liquid refrigerant undergoes expansion followed by compression, so that it is back to its original state. Would you expect that to be a reversible process? (e) Suppose that a house and its exterior are both initially at \(31^{\circ} \mathrm{C}\) . Some time after the air conditioner is turned on, the house is cooled to \(24^{\circ} \mathrm{C}\) . Is this process spontaneous or nonspontaneous?

For each of the following pairs, predict which substance has the higher entropy per mole at a given temperature: (a) \(\operatorname{Ar}(l)\) or \(\operatorname{Ar}(g),(\mathbf{b}) \operatorname{He}(g)\) at 3 atm pressure or \(\operatorname{He}(g)\) at 1.5 atm pressure, (c) 1 mol of \(\mathrm{Ne}(g)\) in 15.0 \(\mathrm{L}\) or 1 \(\mathrm{mol}\) of \(\mathrm{Ne}(g)\) in \(1.50 \mathrm{L},(\mathbf{d}) \mathrm{CO}_{2}(g)\) or \(\mathrm{CO}_{2}(s) .\)

Using data from Appendix \(\mathrm{C}\) , calculate \(\Delta G^{\circ}\) for the following reactions. Indicate whether each reaction is spontaneous at 298 \(\mathrm{K}\) under standard conditions. (a) \(2 \mathrm{SO}_{2}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{SO}_{3}(g)\) (b) \(\mathrm{NO}_{2}(g)+\mathrm{N}_{2} \mathrm{O}(g) \longrightarrow 3 \mathrm{NO}(g)\) (c) \(6 \mathrm{Cl}_{2}(g)+2 \mathrm{Fe}_{2} \mathrm{O}_{3}(s) \rightarrow 4 \mathrm{FeCl}_{3}(s)+3 \mathrm{O}_{2}(g)\) (d) \(\mathrm{SO}_{2}(g)+2 \mathrm{H}_{2}(g) \longrightarrow \mathrm{S}(s)+2 \mathrm{H}_{2} \mathrm{O}(g)\)

(a) What sign for \(\Delta S\) do you expect when the pressure on 0.600 mol of an ideal gas at 350 \(\mathrm{K}\) is increased isothermally from an initial pressure of 0.750 atm? (b) If the final pressure on the gas is 1.20 atm, calculate the entropy change for the process. (c) Do you need to specify the temperature to calculate the entropy change?

The crystalline hydrate \(\mathrm{Cd}\left(\mathrm{NO}_{3}\right) \cdot 4 \mathrm{H}_{2} \mathrm{O}(s)\) loses water when placed in a large, closed, dry vessel at room temperature: $$ \mathrm{Cd}\left(\mathrm{NO}_{3}\right)_{2} \cdot 4 \mathrm{H}_{2} \mathrm{O}(s) \longrightarrow \mathrm{Cd}\left(\mathrm{NO}_{3}\right)_{2}(s)+4 \mathrm{H}_{2} \mathrm{O}(g) $$ This process is spontaneous and \(\Delta H^{\circ}\) is positive at room temperature. (a) What is the sign of \(\Delta S^{\circ}\) at room temperature? (b) If the hydrated compound is placed in a large, closed vessel that already contains a large amount of water vapor, does \(\Delta S^{\circ}\) change for this reaction at room temperature?

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