Chemistry: Principles and Practice
3rd Edition
ISBN: 9780534420123
Author: Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher: Cengage Learning
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- Table 17-1 lists common half-reactions along with the standard reduction potential associated with each half-reaction. These standard reduction potentials are all relative to some standard. What is the standard (zero point)? lf is positive for a half-reaction, what does it mean? If is negative for a half-reaction, what does it mean? Which species in Table 17-1 is most easily reduced? Least easily reduced? The reverse of the half-reactions in Table 17-1 are the oxidation half-reactions. How are standard oxidation potentials determined? In Table 17-1, which species is the best reducing agent? The worst reducing agent? To determine the standard cell potential for a redox reaction, the standard reduction potential is added to the standard oxidation potential. What must be true about this sum if the cell is to be spontaneous (produce a galvanic cell)? Standard reduction and oxidation potentials are intensive. What does this mean? Summarize how line notation is used to describe galvanic cells.arrow_forwardCalculate K at 25°C for each of the reactions referred to in Question 32. Assume smallest whole-number coefficients.arrow_forwardCalculate G and K at 25C for the reactions in Exercises 37 and 41.arrow_forward
- 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).arrow_forwardWhat characterizes an electrolytic cell? What is an ampere? When the current applied to an electrolytic cell is multiplied by the time in seconds, what quantity is determined? How is this quantity converted to moles of electrons required? How are moles of electrons required converted to moles of metal plated out? What does plating mean? How do you predict the cathode and the anode half-reactions in an electrolytic cell? Why is the electrolysis of molten salts much easier to predict in terms of what occurs at the anode and cathode than the electrolysis of aqueous dissolved salts? What is overvoltage?arrow_forwardCalculate the value of the equilibrium constant for the reaction N2(g)+2O2(g)2NO2(g) if the concentrations of the species at equilibrium are [N2] = 0.0013, [O2] = 0.0024, and [NO2] = 0.00065.arrow_forward
- The equilibrium constant for a certain reaction increases by a factor of 6.67 when the temperature is increased from 300.0 K to 350.0 K. Calculate the standard change in enthalpy (H) for this reaction (assuming H is temperature-independent).arrow_forward5.49. Consider the following equilibrium: What is the effect on the equilibrium of each of the following changes? (You may need to calculate some standard enthalpy or Gibbs energy changes to answer these.) (a) The pressure is increased by decreasing the volume. (b) The temperature is decreased. (c) The pressure is increased by the addition of nitrogen gas, .arrow_forwardEstimate ΔrG° at 2000. K for each reaction in Question 60.arrow_forward
- Use the values for G f in Appendix 1 to calculate Ksp for barium sulfate at 25C. Compare with the value given in Chapter 15.arrow_forwardWhat is the standard cell potential you would obtain from a cell at 25C using an electrode in which I(aq) is in contact with I2(s) and an electrode in which a chromium strip dips into a solution of Cr3(aq)?arrow_forwardThe following reaction occurs in pure water: H2O(l)+H2O(l)H3O+(aq)+OH-(aq) which is often abbreviated as H2O(l)H+(aq)+OH-(aq) For this reaction, G = 79.9 kJ/mol at 25C. Calculate the value of G for this reaction at 25C when [OH] = 0.15 M and [H+] = 0.71 M.arrow_forward
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