Consider the reaction HC2H3O2 (aq) →H* (aq) + C2H3O2¯ (aq) The reaction occurs at 25°C. Question 28: Fill in the missing words and values as instructed. Using the Ka of acetic acid in appendix H, calculate the standard free energy change for the ionization of acetic acid in kJ to two significant figures. Standard delta G = KJ Calculate the free energy change for the ionization of acetic acid for the following conditions: pH = 3.00, acetic acid concentration of 0.20 M, acetate concentration concentration of 0.10 M: Delta G = Check KJ

The free energy of formation of one mole of compound refers to a particular chemical equation. For each of the following, write that equation. a KBr(s) b CH3Cl(l) c H2S(g) d AsH3(g)

The molecular scale pictures below show snapshots of a strong acid at three different instants after it is added to water. Place the three pictures in the correct order so that they show the progress of the spontaneous process that takes place as the acid dissolves in the water. Explain your answer in terms of entropy

Use the data in Appendix G to calculate the standard entropy change for H2(g) + CuO(s) H2O() + Cu(s)

Using values of fH and S, calculate the standard molar free energy of formation, fG, for each of the following: (a) Ca(OH)2(s) (b) Cl(g) (c) Na2CO3(s) Compare your calculated values of fG with those listed in Appendix L. Which of these formation reactions are predicted to be product-favored at equilibrium at 25 C?

Consider the reaction of 2 mol H2(g) at 25C and 1 atm with 1 mol O2(g) at the same temperature and pressure to produce liquid water at these conditions. If this reaction is run in a controlled way to generate work, what is the maximum useful work that can be obtained? How much entropy is produced in this case?

Actually, the carbon in CO2(g) is thermodynamically unstable with respect to the carbon in calcium carbonate(limestone). Verify this by determining the standardGibbs free energy change for the reaction of lime,CaO(s), with CO2(g) to make CaCO3(s).

The decomposition of diamond to graphite [C(diamond) C(graphite)] is thermodynamically favored, but occurs slowly at room temperature. a. Use fG values from Appendix L to calculate rG and Keq for the reaction under standard conditions and 298.15 K. b. Use fH and S values from Appendix L to estimate rG and Keq for the reaction at 1000 K. Assume that enthalpy and entropy values are valid at these temperatures. Does heating shift the equilibrium toward the formation of diamond or graphite? c. Why is the formation of diamond favored at high pressures? d. The phase diagram shows that diamond is thermodynamically favored over graphite at 20,000 atmospheres pressure (about 2 GPa) at room temperature. Why is this conversion actually done at much higher temperatures and pressures?

Elemental boron, in the form of thin fibers, can be made by reducing a boron halide with H2. BCl3(g) + 3/2 H2(g) B(s) + 3HCl(g) Calculate H, S, and G at 25 C for this reaction. Is the reaction predicted to be product favored at equilibrium at 25 C? If so, is it enthalpy driven or entropy driven?

a Calculate K1, at 25C for phosphoric acid: H3PO4(aq)H+(aq)+H2PO4(aq) b Which thermodynamic factor is the most significant in accounting for the fact that phosphoric acid is a weak acid? Why ?