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Predict the sign of \(\Delta S^{\circ}\) and then calculate \(\Delta S^{\circ}\) for each of the following reactions. a. \(\mathrm{H}_{2}(g)+\frac{1}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)\) b. \(2 \mathrm{CH}_{3} \mathrm{OH}(g)+3 \mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{CO}_{2}(g)+4 \mathrm{H}_{2} \mathrm{O}(g)\) c. \(\mathrm{HCl}(g) \longrightarrow \mathrm{H}^{+}(a q)+\mathrm{Cl}^{-}(a q)\)

Short Answer

Expert verified
The sign of \(\Delta S^{\circ}\) and the calculated values for the given reactions are: a) Negative; -164.2 \(\frac{J}{mol K}\) b) Positive; 243.6 \(\frac{J}{mol K}\) c) Negative; -130.4 \(\frac{J}{mol K}\)

Step by step solution

01

Predict the sign of \(\Delta S^{\circ}\)

From gas to a liquid phase, the disorder of a system decreases. In this reaction, two gas molecules are combining to form one liquid molecule. Considering fewer molecules and lower randomness, we can predict a negative \(\Delta S^{\circ}\).
02

Calculate \(\Delta S^{\circ}\)

To calculate the change in entropy, we will use the formula: \[\Delta S^{\circ} =\Delta S^{\circ}_{\text{products}} - \Delta S^{\circ}_{\text{reactants}}\] Let's find the entropy changes in the reactants and products: - For H鈧(g): \(S^{\circ}_{\text{H鈧(g)}} = 130.6 \frac{J}{mol K}\) - For O鈧(g): \(S^{\circ}_{\text{O鈧(g)}} = 205.1 \frac{J}{mol K}\) - For H鈧侽(l): \(S^{\circ}_{\text{H鈧侽(l)}} = 69.9 \frac{J}{mol K}\) Now, we can substitute these values in the formula and calculate the change in entropy: \[\Delta S^{\circ}= 69.9 - (130.6 + (0.5 \times 205.1))\] \[\Delta S^{\circ}= -164.2 \frac{J}{mol K}\] #b. \(2 \mathrm{CH}_{3} \mathrm{OH}(g)+3 \mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{CO}_{2}(g)+4 \mathrm{H}_{2} \mathrm{O}(g)\) #
03

Predict the sign of \(\Delta S^{\circ}\)

We have five moles of gas in the reactants and six moles of gas in the products. This means an increase in the number of molecules involved in the reaction which results in higher disorder. We can predict a positive \(\Delta S^{\circ}\).
04

Calculate \(\Delta S^{\circ}\)

Let's find the entropy changes in the reactants and products: - For CH鈧僌H(g): \(S^{\circ}_{\text{CH鈧僌H(g)}} = 239.7 \frac{J}{mol K}\) - For O鈧(g): \(S^{\circ}_{\text{O鈧(g)}} = 205.1 \frac{J}{mol K}\) - For CO鈧(g): \(S^{\circ}_{\text{CO鈧(g)}} = 213.8 \frac{J}{mol K}\) - For H鈧侽(g): \(S^{\circ}_{\text{H鈧侽(g)}} = 188.8 \frac{J}{mol K}\) Now we can substitute these values in the formula and calculate the change in entropy: \[\Delta S^{\circ}= (2 \times 213.8 + 4 \times 188.8) - (2 \times 239.7 + 3 \times 205.1)\] \[\Delta S^{\circ}= 243.6 \frac{J}{mol K}\] #c. \(\mathrm{HCl}(g) \longrightarrow \mathrm{H}^{+}(a q)+\mathrm{Cl}^{-}(a q)\) #
05

Predict the sign of \(\Delta S^{\circ}\)

Gaseous HCl dissociates into aq H鈦 and Cl鈦 ions, resulting in a higher disorder due to the involvement of a significant amount of solvent molecules to solvate these ions. Consequently, we can predict a positive \(\Delta S^{\circ}\).
06

Calculate \(\Delta S^{\circ}\)

Let's find the entropy changes in the reactants and products: - For HCl(g): \(S^{\circ}_{\text{HCl(g)}} = 186.9 \frac{J}{mol K}\) - For H鈦(aq): \(S^{\circ}_{\text{H鈦(aq)}} = 0 \frac{J}{mol K}\) (by convention) - For Cl鈦(aq): \(S^{\circ}_{\text{Cl鈦(aq)}} = 56.5 \frac{J}{mol K}\) Now we can substitute these values in the formula and calculate the change in entropy: \[\Delta S^{\circ} = (0 + 56.5) - (186.9)\] \[\Delta S^{\circ} = -130.4 \frac{J}{mol K}\] To summarize the results: - For reaction (a), the sign of \(\Delta S^{\circ}\) is negative, and the calculated value is -164.2 \(\frac{J}{mol K}\). - For reaction (b), the sign of \(\Delta S^{\circ}\) is positive, and the calculated value is 243.6 \(\frac{J}{mol K}\). - For reaction (c), the sign of \(\Delta S^{\circ}\) is negative, and the calculated value is -130.4 \(\frac{J}{mol K}\).

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Most popular questions from this chapter

List three different ways to calculate the standard free energy change, \(\Delta G^{\circ},\) for a reaction at \(25^{\circ} \mathrm{C} .\) How is \(\Delta G^{\circ}\) estimated at temperatures other than \(25^{\circ} \mathrm{C} ?\) What assumptions are made?

For a liquid, which would you expect to be larger, \(\Delta S_{\text {fusion or }}\) \(\Delta S_{\text {evaporation }} ?\) Why?

From data in Appendix \(4,\) calculate \(\Delta H^{\circ}, \Delta S^{\circ},\) and \(\Delta G^{\circ}\) for each of the following reactions at \(25^{\circ} \mathrm{C}.\) a. \(\mathrm{CH}_{4}(g)+2 \mathrm{O}_{2}(g) \longrightarrow \mathrm{CO}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(g)\) b. \(6 \mathrm{CO}_{2}(g)+6 \mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}(s)+6 \mathrm{O}_{2}(g)\) c. \(\mathrm{P}_{4} \mathrm{O}_{10}(s)+6 \mathrm{H}_{2} \mathrm{O}(l) \longrightarrow 4 \mathrm{H}_{3} \mathrm{PO}_{4}(s)\) d. \(\mathrm{HCl}(g)+\mathrm{NH}_{3}(g) \longrightarrow \mathrm{NH}_{4} \mathrm{Cl}(s)\)

Using data from Appendix \(4,\) calculate \(\Delta H^{\circ}, \Delta G^{\circ},\) and \(K\) (at 298 K) for the production of ozone from oxygen: $$3 \mathrm{O}_{2}(g) \rightleftharpoons 2 \mathrm{O}_{3}(g)$$ At \(30 \mathrm{km}\) above the surface of the earth, the temperature is about \(230 . . \mathrm{K}\) and the partial pressure of oxygen is about \(1.0 \times 10^{-3}\) atm. Estimate the partial pressure of ozone in equilibrium with oxygen at \(30 \mathrm{km}\) above the earth's surface. Is it reasonable to assume that the equilibrium between oxygen and ozone is maintained under these conditions? Explain.

Given the following data: $$2 \mathrm{H}_{2}(g)+\mathrm{C}(s) \longrightarrow \mathrm{CH}_{4}(g) \quad \Delta G^{\circ}=-51 \mathrm{kJ}$$ $$2 \mathrm{H}_{2}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{H}_{2} \mathrm{O}(l) \quad \Delta G^{\circ}=-474 \mathrm{kJ}$$ $$\mathrm{C}(s)+\mathrm{O}_{2}(g) \longrightarrow \mathrm{CO}_{2}(g) \quad \Delta G^{\circ}=-394 \mathrm{kJ}$$ Calculate \(\Delta G^{\circ}\) for \(\mathrm{CH}_{4}(g)+2 \mathrm{O}_{2}(g) \rightarrow \mathrm{CO}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(l)\)

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