In some applications nickel–cadmium batteries have been replaced by nickel–zinc batteries. The overall cell reaction for this relatively new battery is: 2 H2O(l) + 2 NiO(OH)(s) + Zn(s) → 2 Ni(OH)2(s) + Zn(OH)2(s) (c) A single nickel–cadmium cell has a voltage of 1.30 V. Based on the difference in the standard reduction potentials of Cd2+ and Zn2+, what voltage would you estimate a nickel–zinc battery will produce? (d) Would you expect the specific energy density of a nickel–zinc battery to be higher or lower than that of a nickel–cadmium battery?
From each of the following pairs of substances, use data in Appendix E to choose the one that is the stronger reducing agent: (a) Fe(s) or Mg(s) (b) Ca(s) or Al(s) (c) H2(g, acidic solution) or H2S(g)
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Verified Solution
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Key Concepts
Reducing Agents
Standard Reduction Potentials
Electrochemical Series
A cell has a standard cell potential of +0.177 V at 298 K. What is the value of the equilibrium constant for the reaction (b) if n = 2? (c) if n = 3?
A voltaic cell is constructed that uses the following reaction and operates at 298 K: Zn(s) + Ni2+(aq) → Zn2+(aq) + Ni(s) (b) What is the emf of this cell when [Ni2+] = 3.00 M and [Zn2+] = 0.100 M? (c) What is the emf of the cell when [Ni2+] = 0.200 M and [Zn2+] = 0.900 M?
A voltaic cell is constructed that uses the following half-cell reactions:
Cu+(aq) + e- → Cu(s)
I2(s) + 2 e- → 2 I-(aq)
The cell is operated at 298 K with [Cu+] = 0.25 M and [I-] = 0.035 M.
(b) Which electrode is the anode of the cell?
(c) Is the answer to part (b) the same as it would be if the cell were operated under standard conditions?
In the Brønsted–Lowry concept of acids and bases, acid– base reactions are viewed as proton-transfer reactions. The stronger the acid, the weaker is its conjugate base. If we were to think of redox reactions in a similar way, what particle would be analogous to the proton? Would strong oxidizing agents be analogous to strong acids or strong bases? [Sections 20.1 and 20.2]