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You remember that \(\Delta G^{\circ}\) is related to \(R T \ln (K)\) but cannot remember if it's \(R T \ln (K)\) or \(-R T \ln (K) .\) Realizing what \(\Delta G^{\circ}\) and \(K\) mean, how can you figure out the correct sign?

Short Answer

Expert verified
Recall that a negative ∆G° indicates a spontaneous reaction that favors products (K > 1), while a positive ∆G° represents a non-spontaneous reaction that favors reactants (K < 1). Testing the possible expressions, we can conclude that the correct relationship is ∆G° = -RTln(K), as it establishes the appropriate connection between ∆G° and K values.

Step by step solution

01

Identify the meaning of ∆G° and K

First, let's recall that ∆G° is the standard Gibbs free energy change which indicates whether a reaction is thermodynamically favorable or unfavorable. A negative ∆G° implies a spontaneous reaction, and a positive ∆G° means a non-spontaneous reaction. K is the equilibrium constant, which represents the ratio of the concentrations (or activities) of the products to the reactants at equilibrium. A larger K value indicates that the reaction favors the formation of products, while a smaller K value means that the reactants are favored. When K is greater than 1, the reaction favors products, and when K is less than 1, the reaction favors reactants.
02

Analyze the connection between ∆G° and K

Now let's consider the possible cases to understand the relationship between ∆G° and K: 1. If ∆G° is negative (favorable reaction), the reaction will proceed spontaneously, meaning the products are favored over the reactants. In this case, we expect K to be greater than 1. 2. If ∆G° is positive (unfavorable reaction), the reaction is not spontaneous, indicating that the reactants are favored over the products. In this case, we expect K to be less than 1.
03

Determine the appropriate sign for the expression

We have two possible expressions, either ∆G° = RTln(K) or ∆G° = -RTln(K). We will consider both cases to see which one matches the relationship between ∆G° and K deduced in Step 2. Case 1: ∆G° = RTln(K) If ∆G° is negative, then ln(K) must also be negative, which implies K < 1. However, this goes against our understanding of the relationship between ∆G° and K, as a negative ∆G° should favor products (K > 1). Case 2: ∆G° = -RTln(K) If ∆G° is negative, then ln(K) must be positive, which implies K > 1. This matches our understanding of the relationship between ∆G° and K as deduced in Step 2. Based on this analysis, we conclude that the correct sign in the expression is negative, and the correct relationship is: ∆G° = -RTln(K)

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Most popular questions from this chapter

Many biochemical reactions that occur in cells require relatively high concentrations of potassium ion \(\left(\mathrm{K}^{+}\right)\). The concentration of \(\mathrm{K}^{+}\) in muscle cells is about \(0.15 M\). The concentration of \(\mathrm{K}^{+}\) in blood plasma is about \(0.0050 M .\) The high internal concentration in cells is maintained by pumping \(\mathrm{K}^{+}\) from the plasma. How much work must be done to transport \(1.0 \mathrm{~mol} \mathrm{~K}^{+}\) from the blood to the inside of a muscle cell at \(37^{\circ} \mathrm{C}\), normal body temperature? When \(1.0 \mathrm{~mol} \mathrm{~K}^{+}\) is transferred from blood to the cells, do any other ions have to be transported? Why or why not?

Using data from Appendix 4, calculate \(\Delta G\) for the reaction $$2 \mathrm{H}_{2} \mathrm{~S}(g)+\mathrm{SO}_{2}(g) \rightleftharpoons 3 \mathrm{~S}_{\text {mombic }}(s)+2 \mathrm{H}_{2} \mathrm{O}(g)$$ for the following conditions at \(25^{\circ} \mathrm{C}\) : $$\begin{array}{l}P_{\mathrm{H}_{2} \mathrm{~S}}=1.0 \times 10^{-4} \mathrm{~atm} \\\P_{\mathrm{SO}_{2}}=1.0 \times 10^{-2} \mathrm{~atm} \\ P_{\mathrm{H}_{2} \mathrm{O}}=3.0 \times 10^{-2} \mathrm{~atm}\end{array}$$

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. \(\Delta H=-10 . \mathrm{kJ}, \Delta S=-40 . \mathrm{J} / \mathrm{K}, T=200 . \mathrm{K}\)

Consider the system $$\mathrm{A}(g) \longrightarrow \mathrm{B}(g)$$ at \(25^{\circ} \mathrm{C}\). a. Assuming that \(G_{\mathrm{A}}^{\circ}=8996 \mathrm{~J} / \mathrm{mol}\) and \(G_{\mathrm{B}}^{\circ}=11,718 \mathrm{~J} / \mathrm{mol}\), cal- culate the value of the equilibrium constant for this reaction. b. Calculate the equilibrium pressures that result if \(1.00 \mathrm{~mol} \mathrm{~A}(\mathrm{~g})\) at \(1.00\) atm and \(1.00 \mathrm{~mol} \mathrm{~B}(g)\) at \(1.00 \mathrm{~atm}\) are mixed at \(25^{\circ} \mathrm{C}\). c. Show by calculations that \(\Delta G=0\) at equilibrium.

Predict the sign of \(\Delta S\) for each of the following and explain. a. the evaporation of alcohol b. the freezing of water c. compressing an ideal gas at constant temperature d. dissolving \(\mathrm{NaCl}\) in water

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