Electrochemical Half Cells and Reactions



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Suggested reading: Chang text pages 81 89 Cautions Heavy metals, such as lead, and solutions of heavy metals may be toxic and an irritant. Purpose To determine the cell potential (E cell ) for various voltaic cells and compare the data with the calculated E cell values. Introduction Electrochemical cells are devices used to convert chemical energy into electrical energy. The most commonly used electrochemical cells are batteries. A battery contains chemical substances waiting to react; the reaction between the substances involves the transfer of electrons from one species to another. When the battery is placed in a device, a complete circuit is made, and the reaction occurs inducing a flow of electrons (current) to run the device. The energy available from a given electrochemical cell is measu as a potential in units of volts. An electrochemical reaction is composed of two parts: an oxidation half-reaction and a uction half-reaction. When balancing electrochemical reactions, both mass and charge must be conserved. This means that in addition to making sure the number of each type of atom is equal from reactants to products, the number of electrons being transfer between the species must also be equal. When adding the half-equations to yield the overall equation, the electrons appearing in the two half-reactions must cancel each other. Electrochemical half-reactions are written including the number of electrons needed so the overall charge of the reactants equals the overall charge of the products. Oxidation and uction half-reactions each represent half of the overall reaction. An example is the reaction between zinc metal and copper(ii) solution: Zn (s) + Cu 2+ (aq) D Zn 2+ (aq) + Cu (s) (Eqn. 1) This overall reaction has two half-reactions associated with it, the oxidation of the zinc metal: Zn (s) D Zn 2+ (aq) + 2e (Eqn. 2) and the uction of copper(ii) ions: Cu 2+ (aq) + 2e D Cu (s) (Eqn. 3) In this case, both mass balance and charge balance are satisfied in the half-reactions shown for the metals. Standard uction potentials are used to quantitatively determine the amount of energy available from a given electrochemical reaction. Values of the standard uction potentials for half-reactions ( E nearly every general chemistry text (a selective list is shown in Table 1). Reduction Half Equation E o, V Mg +2 (aq) + 2 e - D Mg (s) -2.36 Al 3+ (aq) + 3 e D Al (s) -1.66 Zn 2+ (aq) + 2 e D Zn (s) -.76 Fe 2+ (aq) + 2 e D Fe (s) -.44 Sn 2+ (aq) + 2 e D Sn (s) -.14 Pb 2+ (aq) + 2 e D Pb (s) -.13 2 H + (aq) + 2 e D H 2 (g). Cu 2+ (aq) + 2 e D Cu (s) +.34 ) are provided in tables in Revision F7 Page 1 of 11

Ag + (aq) + 2 e D Ag (s) +.8 Table 1: Standard Reduction Potentials All standard uction potentials are measu relative to the uction of H + : 2 H + (aq) + 2e D H 2 (g) (Eqn. 4) which is given a uction potential of. V. More positive values of compa to H +, while more negative values of E indicate the species is more easily uced E indicate the species is more easily oxidized. Standard uction potentials can be used to determine the energy available for an overall electrochemical reaction. As in thermodynamics calculations, reversing the direction of the reaction changes the sign of the potential. Thus, the oxidation of copper metal has a E ox = -.34 V associated with it. Once the oxidation and uction halfreactions are known, E and the reactions can be added. Overall cell voltages ( E E ox associated with the separate uction and oxidation processes can be written, and cell ) can be used to pict the spontaneity of electrochemical reactions. If E cell is positive, energy is available from the electrochemical reaction occurring and the reaction is spontaneous as written. On the other hand, if the E cell is negative, energy is requi to drive the reaction, therefore the reaction is non-spontaneous as written. Galvanic (or voltaic) cells generate an electrical current via spontaneous electrochemical reactions; most batteries fall under this classification. Electrolytic cells require an external current to proceed (non-spontaneous reactions); a commonly used electrolytic process is galvanization of steel to protect it from oxidation (rusting). Consider the reaction between Zn(s) and copper(ii) ions (Cu 2+ ) under standard conditions. Since the copper is present as an ion, it will most likely be uced, while the solid zinc metal will be oxidized. The uction potentials for the two metals reveal that this is the case; Cu 2+ has a E of +.34V, while Zn 2+ has a E of -.76V. Since uction of Cu 2+ has a more positive potential compa to that of Zn 2+, Cu 2+ will be uced and Zn(s) will be oxidized. These processes are indicated by Equations 5 and 6 below. A net equation and overall standard emf of the reaction ( E obtained by adding these two half-reactions and canceling the electrons: Zn(s) D 2e + Zn 2+ (aq) E o ox =.76 V (Eqn. 5) Cu 2+ (aq) + 2e D Cu(s) E o =.34 V (Eqn. 6) Cu 2+ (aq) + Zn(s) D Cu(s) + Zn 2+ (aq) E o cell = 1.1 V (Eqn. 7) In this particular example, the overall cell voltage is positive, therefore the reaction is spontaneous as written (energy is available to do work). In writing a balanced net cell reaction, we may need to multiply the coefficients of the half-cell reactions to properly cancel the electrons. However, changing the coefficients of a half-cell reaction does not influence the uction and oxidation potential. Reduction and oxidation potentials are intensive properties in that they are independent of the stoichiometry of the reaction. In order to harness the potential from an electrochemical reaction, an electrochemical cell is constructed. A galvanic cell composed of the copper-zinc system mentioned previously is shown in Figure 1. Each half-cell is placed in a separate container. In order to harvest the energy in the overall reaction, a wire and device (in this case a voltmeter) connects the two solid metal pieces, called electrodes. Electrons will flow through this wire from the oxidation half-cell to Revision F8 Page 2 of 11 cell ) are

the uction half-cell. A salt bridge is used to allow ions to move, balancing the changes in charge due to the flow of electrons. Figure 1: An electrochemical cell. http://cwx.prenhall.com/petrucci/medialib/media_portfolio/text_image In this experiment various electrochemical reactions and cells will be observed. First, lead and zinc electrodes will be placed directly in copper and lead ion solutions and observed changes will be recorded. Then, electrochemical cells will be constructed using of Cu/Cu 2+, Zn/Zn 2+, and Pb/Pb 2+ half-cells. Based upon the observed voltages and chemical changes, the metals will be ranked in order of their ease of oxidation. Revision F8 Page 3 of 11

Procedure Note: Metal strips should appear bright and shiny before beginning this experiment. Look carefully for changes either in the appearance of the metal surfaces or the solutions to indicate a reaction. A. The Zn-Cu Redox System A1. Obtain and clean a Zn metal strip with sandpaper. DO NOT SAND TABLETOPS! A2. Obtain a small test tube and fill it with enough.1m CuSO 4 solution to ensure that the Zn metal strip is halfway submerged. A3. Place the clean metal in the small test tube containing.1 M CuSO 4 solution. A4. After 2.5 minutes, record your observations. A5. After 5 minutes, record your observations. A6. Carefully remove the Zn metal strip from the test tube, clean it with sandpaper, and dry using paper towels. Save it to use in Parts C and D. A7. Retain the CuSO 4 solution for use in Part B. B. The Pb-Cu Redox System B1. Obtain and clean a Pb metal strip with sandpaper. DO NOT SAND TABLETOPS! B2. Place the clean Pb metal in the small test tube containing.1 M CuSO 4 solution from Part A. B3. After 5 minutes, record your observations. B4. After 1 minutes, record your observations. B5. Carefully remove the Pb metal strip from the test tube, clean it with sandpaper, and dry using paper towels. Save it to use in Part D. B6. Pour the CuSO 4 solution into the container labeled Discarded CuSO 4 Solution. C. The Zn-Pb Redox System C1. Clean the Zn metal strip with sandpaper. DO NOT SAND TABLETOPS! C2. Obtain a small test tube and fill it with enough.1m Pb(NO 3 ) 2 solution to ensure that the Zn metal strip is halfway submerged. C3. Place the clean Zn metal in the small test tube containing the.1 M Pb(NO 3 ) 2 solution. C4. After 2.5 minutes, record your observations. C5. After 5 minutes, record your observations. C6. Carefully remove the Zn metal strip from the test tube, clean it with sandpaper, and dry using paper towels. Save it to use in Part D. C7. Discard the Pb(NO 3 ) 2 solution into the container labeled Discarded Pb(NO 3 ) 2 Solution. Revision F8 Page 4 of 11

D. Electrochemical Cells D1. Place about 15 2 ml of solutions.1 M Cu(NO 3 ) 2,.1 M Zn(NO 3 ) 2,.1 M Pb(NO 3 ) 2, and.1 M KNO 3 into small labeled 5-mL beakers. D2. Clean the copper, zinc, and lead electrodes using steel wool or sandpaper and rinse with deionized water. D3. Place each metal electrode in its corresponding ionic solution; e.g. copper strip goes into the Cu(NO 3 ) 2 solution. It is important that the correct metal is in the correct solution or your cell will not work properly. D4. Obtain three small strips of filter paper to be used as salt bridges. Completely wet one strip in the beaker containing.1 M KNO 3. Carefully remove the completely wet strip and place one end in the Cu(NO 3 ) 2 solution and the other in the Zn(NO 3 ) 2 solution. The salt bridge should not touch the electrodes. D5. Attach one alligator clip from the voltmeter to the Cu electrode and the second clip to the Zn electrode. If the voltmeter has a negative voltage, reverse the hookup so that each clip is now attached to the other metal in the pair. D6. Record the voltage of the electrochemical cell. D7. Repeat steps D4 D6 for the remaining cells, connecting Cu-Pb and Pb-Zn. Record the positive cell voltages and use a new wet piece of filter paper as a salt bridge for each. D8. Clean the metal strips with sandpaper or steel wool. Dry each strip using paper towels. D9. Place each of the metal ion solutions into their respective waste beakers. Disposal Dispose of all solutions into the appropriate waste container. Return all metal pieces to their original container clean and dry. Clean-Up Clean and dry your work area with water. Wash your hands before leaving the laboratory. Wash all glassware with soap then rinse 3 times with tap water, and once with deionized water. Calculations Oxidation Reduction s 1. Consider the metals and ions involved to write the oxidation and uction half-reactions; obtain the potentials from Table 1 to calculate E cell. 2. Pict if each reaction should be spontaneous based upon calculated E cell. 3. Discuss if your observations are consistent with your piction of spontaneity. Electrochemical Cells 1. Calculate the net cell voltage by using the tabulated potentials. 2. Calculate the percent error between the experimental and calculated cell potentials using the following equation: E measu E cell % error = cell E cell calculated calculated 1% Revision F8 Page 5 of 11

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Name: Data Sheet Lab Partner: Oxidation Reduction s A. Zn-Cu System Experimental Observations Oxidation Half Reduction Half E o ox = E o = Net E o cell = Picted Observed B. Pb-Cu System Experimental Observations Oxidation Half Reduction Half E o ox = E o = Net E o cell = Picted Observed Revision F8 Page 7 of 11

Data Sheet Name: C. Zn-Pb System Experimental Observations Oxidation Half Reduction Half E o ox = E o = Net E o cell = Picted Observed D. Electrochemical Cells Metals Used E cell Measu E cell Calculated from tabulated potentials % Error Cu-Zn Cu-Pb Pb-Zn Revision F8 Page 8 of 11

Calculations: Revision F8 Page 9 of 11

Post-lab Assignment Name: 1. Complete the following table with the observed reactions for the electrochemical cells. Write the correct oxidation and uction half-reaction in the appropriate column for each. Anode Cathode Overall Cell Cu-Zn Cu-Pb Pb-Zn 2. Compare the measu and calculated potentials of your electrochemical cells. Provide an explanation of the percent errors associated with these values. 3. Based on your reactions for the electrochemical cells, give the order of activity of the metals used in this experiment. List the most active (easiest to oxidize) metal first. Revision F8 Page 1 of 11

Name: Pre-lab Assignment 1. Define voltaic cell. 2. Consider the following two uction reactions and their standard electrode potentials: Al +3 (aq) + 3e D Al(s) Cd +2 (aq) + 2e D Cd(s) E = -1.66 V E = -.4 V a. Write the balanced overall cell reaction for a voltaic cell based on these two half-reactions and calculate the standard cell potential. b. Which species is easier to oxidize and why? c. Which species is easier to uce and why? 3. A strip of tin is placed in a CuSO 4 solution. Do you expect a spontaneous chemical reaction to occur? If so, write the net cell reaction. Revision F8 Page 11 of 11