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?

Short Answer

Expert verified
The work required to transport 1.0 mol of K+ ions from the blood to the inside of a muscle cell at 37°C is approximately 2.99 x 10^4 J/mol. The transportation of other ions is necessary during this process to maintain charge neutrality.

Step by step solution

01

Understand Gibbs free energy formula

The work done in transporting ions across a membrane can be calculated using the Gibbs free energy formula: \(\Delta G = \Delta G^0 + RT \ln\frac{Q}{K}\) where: - \(\Delta G\) is the Gibbs free energy change - \(\Delta G^0\) is the standard Gibbs free energy change (0 for this process) - R is the gas constant (8.314 J/mol K) - T is the temperature in Kelvin (in this case, 37°C = 310 K) - Q is the reaction quotient (calculated by dividing the concentration of K+ in muscle cells by the concentration in blood plasma) - K is the equilibrium constant (1 for this process since the concentrations remain constant)
02

Calculate the reaction quotient (Q)

We are given that the concentration of K+ in muscle cells is 0.15 M, and the concentration in blood plasma is 0.0050 M. We can calculate the reaction quotient Q as follows: \(Q = \frac{\text{concentration in muscle cells}}{\text{concentration in blood}} = \frac{0.15 M}{0.0050 M} = 30\)
03

Calculate the Gibbs free energy change (\(\Delta G\))

Using the given formula, we can now find the Gibbs free energy change: \(\Delta G = \Delta G^0 + RT \ln\frac{Q}{K} = 0 + (8.314 J/mol \cdot K)(310 K) \ln(30)\) Solve for \(\Delta G\): \(\Delta G = 8.314 \times 310 \times \ln(30) \approx 2.99 \times 10^4 J/mol\)
04

Determine the necessity of transporting other ions

The transportation of K+ from blood to cells results in a change in the overall charge balance across the cell membrane. As K+ ions are moved into the cell, more positive charges are transferred inside the cell. In order to maintain charge neutrality, an equivalent amount of anionic charge (negative ions) must be moved across the membrane or an equivalent amount of cationic charge (positive ions) must be moved out of the cell to maintain the overall charge balance. Therefore, the transportation of other ions is necessary to maintain charge neutrality during this process. #Result# The work required to transport 1.0 mol K+ from the blood to the inside of a muscle cell at 37°C is approximately 2.99 x 10^4 J/mol. Yes, the transportation of other ions is necessary to maintain charge neutrality during this process.

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Most popular questions from this chapter

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

A mixture of hydrogen gas and chlorine gas remains unreacted until it is exposed to ultraviolet light from a burning magnesium strip. Then the following reaction occurs very rapidly: $$\mathrm{H}_{2}(g)+\mathrm{Cl}_{2}(g) \longrightarrow 2 \mathrm{HCl}(g)$$ Explain.

Consider a weak acid, HX. If a \(0.10 M\) solution of HX has a pH of \(5.83\) at \(25^{\circ} \mathrm{C}\), what is \(\Delta G^{\circ}\) for the acid's dissociation reaction at \(25^{\circ} \mathrm{C}\) ?

Impure nickel, refined by smelting sulfide ores in a blast furnace, can be converted into metal from \(99.90 \%\) to \(99.99 \%\) purity by the Mond process. The primary reaction involved in the Mond process is $$\mathrm{Ni}(s)+4 \mathrm{CO}(g) \rightleftharpoons \mathrm{Ni}(\mathrm{CO})_{4}(g)$$ a. Without referring to Appendix 4, predict the sign of \(\Delta S^{\circ}\) for the above reaction. Explain. b. The spontaneity of the above reaction is temperature dependent. Predict the sign of \(\Delta S_{\text {sarr }}\) for this reaction. Explain. c. For \(\mathrm{Ni}(\mathrm{CO})_{4}(g), \Delta H_{\mathrm{f}}^{\circ}=-607 \mathrm{~kJ} / \mathrm{mol}\) and \(S^{\circ}=417 \mathrm{~J} / \mathrm{K} \cdot \mathrm{mol}\) at \(298 \mathrm{~K}\). Using these values and data in Appendix 4, calculate \(\Delta H^{\circ}\) and \(\Delta S^{\circ}\) for the above reaction. d. Calculate the temperature at which \(\Delta G^{\circ}=0(K=1)\) for the above reaction, assuming that \(\Delta H^{\circ}\) and \(\Delta S^{\circ}\) do not depend on temperature. e. The first step of the Mond process involves equilibrating impure nickel with \(\mathrm{CO}(\mathrm{g})\) and \(\mathrm{Ni}(\mathrm{CO})_{4}(g)\) at about \(50^{\circ} \mathrm{C}\). The purpose of this step is to convert as much nickel as possible into the gas phase. Calculate the equilibrium constant for the preceding reaction at \(50 .{ }^{\circ} \mathrm{C}\). f. In the second step of the Mond process, the gaseous \(\mathrm{Ni}(\mathrm{CO})_{4}\) is isolated and heated to \(227^{\circ} \mathrm{C}\). The purpose of this step is to deposit as much nickel as possible as pure solid (the reverse of the preceding reaction). Calculate the equilibrium constant for the preceding reaction at \(227^{\circ} \mathrm{C}\). g. Why is temperature increased for the second step of the Mond process? h. The Mond process relies on the volatility of \(\mathrm{Ni}(\mathrm{CO})_{4}\) for its success. Only pressures and temperatures at which \(\mathrm{Ni}(\mathrm{CO})_{4}\) is a gas are useful. A recently developed variation of the Mond process carries out the first step at higher pressures and a temperature of \(152^{\circ} \mathrm{C}\). Estimate the maximum pressure of \(\mathrm{Ni}(\mathrm{CO})_{4}(g)\) that can be attained before the gas will liquefy at \(152^{\circ} \mathrm{C}\). The boiling point for \(\mathrm{Ni}(\mathrm{CO})_{4}\) is \(42^{\circ} \mathrm{C}\) and the enthalpy of vaporization is \(29.0 \mathrm{~kJ} / \mathrm{mol}\).

It is quite common for a solid to change from one structure to another at a temperature below its melting point. For example, sulfur undergoes a phase change from the rhombic crystal structure to the monoclinic crystal form at temperatures above \(95^{\circ} \mathrm{C}\). a. Predict the signs of \(\Delta H\) and \(\Delta S\) for the process \(S_{\text {rhcmbic }} \longrightarrow\) \(\mathrm{S}_{\text {monoclinic }}\) b. Which form of sulfur has the more ordered crystalline structure (has the smaller positional probability)?

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