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Given the values of \(\Delta H\) and \(\Delta S,\) which of the following changes will be spontaneous at constant \(T\) and \(P ?\) a. \(\Delta H=+25 \mathrm{kJ}, \Delta S=+5.0 \mathrm{J} / \mathrm{K}, T=300 . \mathrm{K}\) b. \(\Delta H=+25 \mathrm{kJ}, \Delta S=+100 . \mathrm{J} / \mathrm{K}, T=300 . \mathrm{K}\) c. \(\Delta H=-10 . \mathrm{kJ}, \Delta S=+5.0 \mathrm{J} / \mathrm{K}, T=298 \mathrm{K}\) d. \(\Delta H=-10 . \mathrm{kJ}, \Delta S=-40 . \mathrm{J} / \mathrm{K}, T=200 . \mathrm{K}\)

Short Answer

Expert verified
Options b, c, and d represent spontaneous reactions at constant T and P, with ∆G values of -5000 J, -11490 J, and -2000 J, respectively.

Step by step solution

01

Recall the Gibbs free energy equation

Recall the formula for Gibbs free energy change: ∆G = ∆H - T∆S, where ∆G is Gibbs free energy change, ∆H is enthalpy change, T is temperature in Kelvin, and ∆S is entropy change. Step 2: Calculate ∆G for each option
02

Calculate ∆G for each option

Plug the given values for ∆H, ∆S, and T into the formula and calculate ∆G for each of the four cases. a) ∆H = +25 kJ, ∆S = +5.0 J/K, T = 300 K ∆G = (25*1000) - 300*(5) = 25000 - 1500 = 23500 J b) ∆H = +25 kJ, ∆S = +100 J/K, T = 300 K ∆G = (25*1000) - 300*(100) = 25000 - 30000 = -5000 J c) ∆H = -10 kJ, ∆S = +5.0 J/K, T = 298 K ∆G = (-10*1000) - 298*(5) = -10000 - 1490 = -11490 J d) ∆H = -10 kJ, ∆S = -40 J/K, T = 200 K ∆G = (-10*1000) - 200*(-40) = -10000 + 8000 = -2000 J Step 3: Determine if the reaction is spontaneous
03

Determine if the reaction is spontaneous

Analyze the calculated ∆G values to determine if the reaction is spontaneous or not. If ∆G is negative, the reaction is spontaneous. a) ∆G = 23500 J - The reaction is NOT spontaneous. b) ∆G = -5000 J - The reaction IS spontaneous. c) ∆G = -11490 J - The reaction IS spontaneous. d) ∆G = -2000 J - The reaction IS spontaneous. As a result, options b, c, and d represent spontaneous reactions at constant T and P.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Enthalpy Change
Enthalpy change, represented by \(\Delta H\), is the measure of heat absorbed or released during a chemical reaction at constant pressure. It helps us understand whether a reaction is endothermic or exothermic. - **Endothermic Reactions**: These reactions absorb heat from the surroundings, leading to a positive \(\Delta H\). For example, in option a and b of the exercise, \(\Delta H\) is +25 kJ, indicating an endothermic reaction.- **Exothermic Reactions**: These reactions release heat to the surroundings, resulting in a negative \(\Delta H\). In options c and d of the exercise, \(\Delta H\) is -10 kJ, indicating an exothermic reaction.Understanding enthalpy change is crucial because it gives insight into the energy dynamics of a reaction, guiding predictions about the spontaneity and feasibility of reactions under specific conditions.
Entropy Change
Entropy change, denoted \(\Delta S\), reflects the degree of disorder or randomness in a system during a chemical reaction. It is a crucial part of predicting reaction spontaneity because it shows how the system's order changes. - **Positive Entropy Change**: When \(\Delta S\) is positive, the disorder increases. This is observed in the exercise's options a, b, and c. For example, in option b, \(\Delta S\) is +100 J/K, signifying increased disorder, which often favors spontaneity, especially at higher temperatures.- **Negative Entropy Change**: Here, \(\Delta S\) is negative, indicating decreased disorder. Option d in the exercise illustrates this, with a \(\Delta S\) of -40 J/K. Decreased disorder might make a reaction non-spontaneous unless other factors like negative \(\Delta H\) contribute to spontaneity.Entropy change helps us see the bigger picture of a reaction, allowing us to assess spontaneous potential when paired with enthalpy change and temperature.
Spontaneity of Reactions
The spontaneity of a chemical reaction is determined by the Gibbs free energy change, \(\Delta G\). A reaction is considered spontaneous if \(\Delta G < 0\). We calculate \(\Delta G\) through the equation:\[ \Delta G = \Delta H - T \Delta S \]- **Calculating \(\Delta G\)**: We take the given \(\Delta H\), \(\Delta S\), and temperature \(T\) and plug them into the formula. For example, in the exercise, option b gives \(\Delta G = -5000 \text{ J}\), indicating a spontaneous reaction.- **Temperature's Role**: Since \(\Delta S\) is temperature-dependent, temperature can influence spontaneity. For instance, in option a, even though \(\Delta S\) is positive, the temperature factor results in a positive \(\Delta G\), making the reaction non-spontaneous.Understanding spontaneity helps us predict whether a reaction will occur without external intervention, making \(\Delta G\) an essential tool for chemists.

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Most popular questions from this chapter

At 1 atm, liquid water is heated above \(100^{\circ} \mathrm{C}\) . For this process, which of the following choices (i-iv) is correct for \(\Delta S_{\text { surr }} ? \Delta S ?\) \(\Delta S_{\text { univ }} ?\) Explain each answer. i. greater than zero ii. less than zero iii. equal to zero iv. cannot be determined

Monochloroethane \(\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{Cl}\right)\) can be produced by the direct reaction of ethane gas \(\left(\mathrm{C}_{2} \mathrm{H}_{6}\right)\) with chlorine gas or by the reaction of ethylene gas \(\left(\mathrm{C}_{2} \mathrm{H}_{4}\right)\) with hydrogen chloride gas. The second reaction gives almost a 100\(\%\) yield of pure \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{Cl}\) at a rapid rate without catalysis. The first method requires light as an energy source or the reaction would not occur. Yet \(\Delta G^{\circ}\) for the first reaction is considerably more negative than \(\Delta G^{\circ}\) for the second reaction. Explain how this can be so.

Consider the following reaction at 298 K: $$2 \mathrm{SO}_{2}(g)+\mathrm{O}_{2}(g) \rightleftharpoons 2 \mathrm{SO}_{3}(g)$$ An equilibrium mixture contains \(\mathrm{O}_{2}(g)\) and \(\mathrm{SO}_{3}(g)\) at partial pressures of 0.50 \(\mathrm{atm}\) and 2.0 \(\mathrm{atm}\) , respectively. Using data from Appendix \(4,\) determine the equilibrium partial pressure of \(\mathrm{SO}_{2}\) in the mixture. Will this reaction be most favored at a high or a low temperature, assuming standard conditions?

Consider the dissociation of a weak acid \(\mathrm{HA}\left(K_{\mathrm{a}}=4.5 \times 10^{-3}\right)\) in water: $$\mathrm{HA}(a q) \rightleftharpoons \mathrm{H}^{+}(a q)+\mathrm{A}^{-}(a q)$$ Calculate \(\Delta G^{\circ}\) for this reaction at \(25^{\circ} \mathrm{C}\)

At \(100 .^{\circ} \mathrm{C}\) and \(1.00 \mathrm{atm}, \Delta H^{\circ}=40.6 \mathrm{kJ} / \mathrm{mol}\) for the vaporization of water. Estimate \(\Delta G^{\circ}\) for the vaporization of water at \(90 .^{\circ} \mathrm{C}\) and \(110 .^{\circ} \mathrm{C}\) . Assume \(\Delta H^{\circ}\) and \(\Delta S^{\circ}\) at \(100 .^{\circ} \mathrm{C}\) and 1.00 \(\mathrm{atm}\) do not depend on temperature.

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