Electrochemistry Chapter 19

2Mg (s) + O 2 (g) 2MgO (s) 2Mg 2Mg e - O 2 + 4e - 2O 2- Oxidation half-reaction (lose e - ) Reduction half-reaction (gain e - ) 19.1 Electrochemical processes are oxidation-reduction reactions in which: the energy released by a spontaneous reaction is converted to electricity or electrical energy is used to cause a nonspontaneous reaction to occur

Oxidation number The charge the atom would have in a molecule (or an ionic compound) if electrons were completely transferred. 1.Free elements (uncombined state) have an oxidation number of zero. Na, Be, K, Pb, H 2, O 2, P 4 = 0 2.In monatomic ions, the oxidation number is equal to the charge on the ion. Li +, Li = +1; Fe 3+, Fe = +3; O 2-, O = -2 3.The oxidation number of oxygen is usually –2. In H 2 O 2 and O 2 2- it is –1. 4.4

4.The oxidation number of hydrogen is +1 except when it is bonded to metals in binary compounds. In these cases, its oxidation number is –1. 6. The sum of the oxidation numbers of all the atoms in a molecule or ion is equal to the charge on the molecule or ion. 5.Group IA metals are +1, IIA metals are +2 and fluorine is always –1. HCO 3 - O = -2H = +1 3x(-2) ? = -1 C = +4 Oxidation numbers of all the atoms in HCO 3 - ? 4.4

Balancing Redox Equations Write the unbalanced equation for the reaction ion ionic form. The oxidation of Fe 2+ to Fe 3+ by Cr 2 O 7 2- in acid solution? Fe 2+ + Cr 2 O 7 2- Fe 3+ + Cr 3+ 2.Separate the equation into two half-reactions. Oxidation: Cr 2 O 7 2- Cr Reduction: Fe 2+ Fe Balance the atoms other than O and H in each half-reaction. Cr 2 O Cr 3+

Balancing Redox Equations 4.For reactions in acid, add H 2 O to balance O atoms and H + to balance H atoms. Cr 2 O Cr H 2 O 14H + + Cr 2 O Cr H 2 O 5.Add electrons to one side of each half-reaction to balance the charges on the half-reaction. Fe 2+ Fe e - 6e H + + Cr 2 O Cr H 2 O 6.If necessary, equalize the number of electrons in the two half- reactions by multiplying the half-reactions by appropriate coefficients. 6Fe 2+ 6Fe e - 6e H + + Cr 2 O Cr H 2 O 19.1

Balancing Redox Equations 7.Add the two half-reactions together and balance the final equation by inspection. The number of electrons on both sides must cancel. 6e H + + Cr 2 O Cr H 2 O 6Fe 2+ 6Fe e - Oxidation: Reduction: 14H + + Cr 2 O Fe 2+ 6Fe Cr H 2 O 8.Verify that the number of atoms and the charges are balanced. 14x1 – 2 + 6x2 = 24 = 6x3 + 2x For reactions in basic solutions, add OH - to both sides of the equation for every H + that appears in the final equation.

Voltaic Cells In spontaneous oxidation-reduction (redox) reactions, electrons are transferred and energy is released.

Voltaic Cells We can use that energy to do work if we make the electrons flow through an external device. We call such a setup a voltaic cell.

Voltaic Cells A typical cell looks like this. The oxidation occurs at the anode. The reduction occurs at the cathode.

Voltaic Cells Once even one electron flows from the anode to the cathode, the charges in each beaker would not be balanced and the flow of electrons would stop.

Voltaic Cells Therefore, we use a salt bridge, usually a U-shaped tube that contains a salt solution, to keep the charges balanced. –Cations move toward the cathode. –Anions move toward the anode.

Voltaic Cells In the cell, then, electrons leave the anode and flow through the wire to the cathode. As the electrons leave the anode, the cations formed dissolve into the solution in the anode compartment.

Voltaic Cells As the electrons reach the cathode, cations in the cathode are attracted to the now negative cathode. The electrons are taken by the cation, and the neutral metal is deposited on the cathode.

Galvanic Cells 19.2 spontaneous redox reaction anode oxidation cathode reduction

Electromotive Force (emf) Water only spontaneously flows one way in a waterfall. Likewise, electrons only spontaneously flow one way in a redox reaction—from higher to lower potential energy.

Electromotive Force (emf) The potential difference between the anode and cathode in a cell is called the electromotive force (emf). It is also called the cell potential and is designated E cell.

Cell Potential Cell potential is measured in volts (V). 1 V = 1 JCJC

Standard Reduction Potentials Reduction potentials for many electrodes have been measured and tabulated.

Standard Hydrogen Electrode Their values are referenced to a standard hydrogen electrode (SHE). By definition, the reduction potential for hydrogen is 0 V: 2 H + (aq, 1M) + 2 e −  H 2 (g, 1 atm)

Standard Cell Potentials The cell potential at standard conditions can be found through this equation: E cell  = E red (cathode) - E red (anode)  Because cell potential is based on the potential energy per unit of charge, it is an intensive property.

Cell Potentials For the oxidation in this cell, For the reduction, E red = V  E red = V 

Cell Potentials E cell  = E red  (cathode) − E red  (anode) = V - (-0.76 V) = V

Oxidizing and Reducing Agents The strongest oxidizers have the most positive reduction potentials. The strongest reducers have the most negative reduction potentials.

Oxidizing and Reducing Agents The greater the difference between the two, the greater the voltage of the cell.

Galvanic Cells 19.2 The difference in electrical potential between the anode and cathode is called: cell voltage electromotive force (emf) cell potential Cell Diagram Zn (s) + Cu 2+ (aq) Cu (s) + Zn 2+ (aq) [Cu 2+ ] = 1 M & [Zn 2+ ] = 1 M Zn (s) | Zn 2+ (1 M) || Cu 2+ (1 M) | Cu (s) anodecathode

19.3 E 0 is for the reaction as written The more positive E 0 the greater the tendency for the substance to be reduced The half-cell reactions are reversible The sign of E 0 changes when the reaction is reversed Changing the stoichiometric coefficients of a half-cell reaction does not change the value of E 0

What is the standard emf of an electrochemical cell made of a Cd electrode in a 1.0 M Cd(NO 3 ) 2 solution and a Cr electrode in a 1.0 M Cr(NO 3 ) 3 solution? Cd 2+ (aq) + 2e - Cd (s) E 0 = V Cr 3+ (aq) + 3e - Cr (s) E 0 = V Cd is the stronger oxidizer Cd will oxidize Cr 2e - + Cd 2+ (1 M) Cd (s) Cr (s) Cr 3+ (1 M) + 3e - Anode (oxidation): Cathode (reduction): 2Cr (s) + 3Cd 2+ (1 M) 3Cd (s) + 2Cr 3+ (1 M) x 2 x 3 E 0 = E cathode - E anode cell 00 E 0 = – (-0.74) cell E 0 = 0.34 V cell 19.3

19.4 Spontaneity of Redox Reactions  G = -nFE cell  G 0 = -nFE cell 0 n = number of moles of electrons in reaction F = 96,500 J V mol = 96,500 C/mol  G 0 = -RT ln K = -nFE cell 0 E cell 0 = RT nF ln K (8.314 J/K mol)(298 K) n (96,500 J/V mol) ln K = = V n ln K E cell 0 = V n log K E cell 0

Spontaneity of Redox Reactions 19.4

2e - + Fe 2+ Fe 2Ag 2Ag + + 2e - Oxidation: Reduction: What is the equilibrium constant for the following reaction at 25 0 C? Fe 2+ (aq) + 2Ag (s) Fe (s) + 2Ag + (aq) = V n ln K E cell E 0 = – (0.80) E 0 = V V x nE0E0 cell exp K = n = V x 2x V = exp K = 1.23 x E 0 = E Fe /Fe – E Ag /Ag

The Effect of Concentration on Cell Emf  G =  G 0 + RT ln Q  G = -nFE  G 0 = -nFE 0 -nFE = -nFE 0 + RT ln Q E = E 0 - ln Q RT nF Nernst equation At V n ln Q E 0 E = V n log Q E 0 E =

Will the following reaction occur spontaneously at 25 0 C if [Fe 2+ ] = 0.60 M and [Cd 2+ ] = M? Fe 2+ (aq) + Cd (s) Fe (s) + Cd 2+ (aq) 2e - + Fe 2+ 2Fe Cd Cd e - Oxidation: Reduction: n = 2 E 0 = – (-0.40) E 0 = V E 0 = E Fe /Fe – E Cd /Cd V n ln Q E 0 E = V 2 ln VE = E = E > 0Spontaneous 19.5

19.8 Electrolysis is the process in which electrical energy is used to cause a nonspontaneous chemical reaction to occur.

Electrolysis of Water 19.8

Electrolysis and Mass Changes charge (C) = current (A) x time (s) 1 mole e - = 96,500 C 19.8

How much Ca will be produced in an electrolytic cell of molten CaCl 2 if a current of A is passed through the cell for 1.5 hours? Anode: Cathode: Ca 2+ (l) + 2e - Ca (s) 2Cl - (l) Cl 2 (g) + 2e - Ca 2+ (l) + 2Cl - (l) Ca (s) + Cl 2 (g) 2 mole e - = 1 mole Ca mol Ca = C s x 1.5 hr x 3600 s hr96,500 C 1 mol e - x 2 mol e - 1 mol Ca x = mol Ca = 0.50 g Ca 19.8

Batteries 19.6 Leclanché cell Dry cell Zn (s) Zn 2+ (aq) + 2e - Anode: Cathode: 2NH 4 (aq) + 2MnO 2 (s) + 2e - Mn 2 O 3 (s) + 2NH 3 (aq) + H 2 O (l) + Zn (s) + 2NH 4 (aq) + 2MnO 2 (s) Zn 2+ (aq) + 2NH 3 (aq) + H 2 O (l) + Mn 2 O 3 (s)

Batteries Zn(Hg) + 2OH - (aq) ZnO (s) + H 2 O (l) + 2e - Anode: Cathode: HgO (s) + H 2 O (l) + 2e - Hg (l) + 2OH - (aq) Zn(Hg) + HgO (s) ZnO (s) + Hg (l) Mercury Battery 19.6

Batteries 19.6 Anode: Cathode: Lead storage battery PbO 2 (s) + 4H + (aq) + SO 2- (aq) + 2e - PbSO 4 (s) + 2H 2 O (l) 4 Pb (s) + SO 2- (aq) PbSO 4 (s) + 2e - 4 Pb (s) + PbO 2 (s) + 4H + (aq) + 2SO 2- (aq) 2PbSO 4 (s) + 2H 2 O (l) 4

Batteries 19.6 Solid State Lithium Battery

Batteries 19.6 A fuel cell is an electrochemical cell that requires a continuous supply of reactants to keep functioning Anode: Cathode: O 2 (g) + 2H 2 O (l) + 4e - 4OH - (aq) 2H 2 (g) + 4OH - (aq) 4H 2 O (l) + 4e - 2H 2 (g) + O 2 (g) 2H 2 O (l)

Corrosion 19.7

Cathodic Protection of an Iron Storage Tank 19.7

Chemistry In Action: Dental Filling Discomfort Hg 2 /Ag 2 Hg V 2+ Sn /Ag 3 Sn V 2+ Sn /Ag 3 Sn V 2+