The \(K_{b}\) for methylamine \(\left(\mathrm{CH}_{3} \mathrm{NH}_{2}\right)\) at \(25^{\circ} \mathrm{C}\) is given in Appendix \(\mathrm{D}\) . (a) Write the chemical equation for the equilibrium that corresponds to \(K_{b}\) . (b) By using the value of \(K_{b},\) calculate \(\Delta G^{\circ}\) for the equilibrium in part (a). (c) What is the value of \(\Delta G\) at equilibrium? (d) What is the value of \(\Delta G\) when \(\left[\mathrm{H}^{+}\right]=6.7 \times 10^{-9} M,\left[\mathrm{CH}_{3} \mathrm{NH}_{3}^{+}\right]=2.4 \times 10^{-3} \mathrm{M}\) and \(\left[\mathrm{CH}_{3} \mathrm{NH}_{2}\right]=0.098 \mathrm{M} ?\)

Short Answer

Expert verified
The chemical equilibrium equation corresponding to Kb is: \( CH_{3}NH_{2} + H_{2}O \rightleftharpoons CH_{3}NH_{3}^{+} + OH^{-}\). Using the given Kb value, we find that ΔG° = -13.78 kJ/mol. At equilibrium, ΔG = 0. For the given concentrations, we calculate [OH-] = 1.49 x 10^{-6} M, and Q = 3.62 x 10^{-2}. Substituting these values into the ΔG formula, we find that ΔG = -11.25 kJ/mol.

Step by step solution

01

Write the chemical equation for the equilibrium reaction corresponding to Kb

To start, let's write down the base dissociation reaction of methylamine (CH3NH2) when it reacts with water (H2O). Since methylamine is a weak base, it will accept a proton (H+) from water, forming its conjugate acid (CH3NH3+) and hydroxide ions (OH-). \( CH_{3}NH_{2} + H_{2}O \rightleftharpoons CH_{3}NH_{3}^{+} + OH^{-}\)
02

Calculate ΔG° using Kb

The equilibrium constant for the base dissociation reaction, Kb, is related to the standard Gibbs free energy change (ΔG°) by the following equation: \( ΔG° = -RT \ln{K_b}\) , where \(R\) is the gas constant (= 8.314 J/(mol K)) and \(T\) is the temperature in Kelvin. We are given that the temperature is 25°C, which is equal to 298.15 K. The value of Kb for methylamine can be found in Appendix D. Kb = 4.4 x 10^(-4). Now, we plug in these values into the formula to calculate ΔG°.
03

Calculate the value of ΔG at equilibrium

At equilibrium, the value of ΔG equals 0. This means the system is in a state of minimum energy. Hence, ΔG = 0
04

Calculate ΔG using given concentrations

The relationship between ΔG, ΔG°, and the reaction quotient (Q) is given by the formula: \( ΔG = ΔG° + RT \ln{Q}\) We are given the concentrations of H+ ([H+]), CH3NH3+ ([CH3NH3+]), and CH3NH2 ([CH3NH2]). However, we should note that the base dissociation reaction involves OH- ions instead of H+ ions. Therefore, we need to use the relation between the concentrations of H+ ions and OH- ions: \(K_w = [H^+][OH^-]\), where Kw is the ion product of water (1.0 x 10^(-14) at 25°C). Now, let's calculate the concentration of OH- ions: \([OH^{-}] = \frac{K_w}{[H^+]} = \frac{1.0 \times 10^{-14}}{6.7 \times 10^{-9}}\) Next, we determine the reaction quotient, Q: \(Q = \frac{[CH_{3}NH_{3}^{+}][OH^{-}]}{[CH_{3}NH_{2}]}\) Plug in the given concentrations of the species involved in the reaction and the calculated value of [OH-] into the equation. Finally, we can calculate ΔG using the expression: \( ΔG = ΔG° + RT \ln{Q}\) Plug in the calculated value of ΔG°, and the reaction quotient, Q, to determine the final value of ΔG. Now you have successfully calculated the ΔG value for the given concentrations of H+, CH3NH3+, and CH3NH2.

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Most popular questions from this chapter

(a) Can endothermic chemical reactions be spontaneous? (b) Can a process be spontaneous at one temperature and nonspontaneous at a different temperature? (c) Water can be decomposed to form hydrogen and oxygen, and the hydrogen and oxygen can be recombined to form water. Does this mean that the processes are thermodynamically reversible? (d) Does the amount of work that a system can do on its surroundings depend on the path of the process?

For each of the following pairs, predict which substance possesses the larger entropy per mole: (a) 1 1 mol of \(\mathrm{O}_{2}(g)\) at \(300^{\circ} \mathrm{C}, 0.01\) atm, or 1 \(\mathrm{mol}\) of \(\mathrm{O}_{3}(g)\) at \(300^{\circ} \mathrm{C}, 0.01\) atm; (b) 1 \(\mathrm{mol}\) of \(\mathrm{H}_{2} \mathrm{O}(g)\) at \(100^{\circ} \mathrm{C}, 1 \mathrm{atm},\) or 1 \(\mathrm{mol}\) of \(\mathrm{H}_{2} \mathrm{O}(l)\) at \(100^{\circ} \mathrm{C}, 1\) atm; \((\mathbf{c}) 0.5 \mathrm{mol}\) of \(\mathrm{N}_{2}(g)\) at \(298 \mathrm{K}, 20 \mathrm{-L}\) volume, or 0.5 \(\mathrm{mol} \mathrm{CH}_{4}(g)\) at \(298 \mathrm{K}, 20-\mathrm{volume} ;(\mathbf{d}) 100 \mathrm{g} \mathrm{Na}_{2} \mathrm{SO}_{4}(s)\) at \(30^{\circ} \mathrm{C}\) or 100 \(\mathrm{g} \mathrm{Na}_{2} \mathrm{SO}_{4}(a q)\) at \(30^{\circ} \mathrm{C} .\)

Indicate whether each statement is true or false. (a) The second law of thermodynamics says that entropy is conserved. (b) If the entropy of the system increases during a reversible process, the entropy change of the surroundings must decrease by the same amount. (c) In a certain spontaneous process the system undergoes an entropy change of \(4.2 \mathrm{J} / \mathrm{K} ;\) therefore, the entropy change of the surroundings must be \(-4.2 \mathrm{J} / \mathrm{K}\)

For a certain chemical reaction, \(\Delta H^{\circ}=-35.4 \mathrm{kJ}\) and \(\Delta S^{\circ}=-85.5 \mathrm{J} / \mathrm{K}\) . (a) Is the reaction exothermic or endothermic? (b) Does the reaction lead to an increase or decrease in the randomness or disorder of the system?(c) Calculate \(\Delta G^{\circ}\) for the reaction at 298 \(\mathrm{K}\) . (d) Is the reaction spontaneous at 298 \(\mathrm{K}\) under standard conditions?

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?

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