Oxidation (oxidized): the loss of one or more electrons. Reduction (reduced): the gain of one or more electrons

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1 1 of 13 interesting links: Battery Chemistry Tutorial at Duracell Procell: Battery Chemistry at /default.asp I. Oxidation states: a review (see Ch. 4 notes for review) A. Terms Oxidationreduction reaction (redox reaction): a reaction in which electrons are transferred between spp. and/or in which atoms involved in the reaction change oxidation number Oxidation number: a concept devised as way of keeping track of electrons in reactions: the actual charge on a monatomic ion, or the hypothetical charge assigned to an uncharged atom using a set of rules Oxidation (oxidized): the loss of one or more electrons Reduction (reduced): the gain of one or more electrons Oxidizing agent: a chemical that oxidizes something else and reduces itself Reducing agent: a chemical that reduces something else and oxidizes itself B. Rules for determining oxidation numbers Rule 1: the oxidation number of atoms in their elemental state is zero Rule 2: the oxidation number of a monatomic ion is equal to its charge Rule 3: the oxidation number of oxygen is always equal to 2 unless in a peroxide (then 1) Rule 4: the oxidation number of hydrogen is always +1 unless in a hydride (then 1) Rule 5: Fluorine always has an oxidation number of The other

2 2 of 13 halogens always have an oxidation of 1 as anions in binary compounds. Halogens listed as the first member of a binary molecular compound or involved in oxyanions have positive oxidation numbers. 6. Rule 6: for either a neutral compound or for any polyatomic ion, the sum of the oxidation numbers of the atoms in the molecule is equal to the net charge on the specie C. Examples of determining oxidation numbers: NO 3 H 2 SO 4 Fe(OH) 2 Li 3 PO 4 HClO 3 W 2 (SO 3 ) 3 D. Balancing simple redox equations: rules Assign oxidation numbers to all atoms in all reactants and products Break the reaction down into oxidation and reduction halfreactions Multiply if necessary to get the number of electrons in each halfreaction to be equal d. Add the halfreactions together II. Balancing redox equations A. B. Simple halfreactions: breaking redox reactions down into halfreactions (see BLB Chapter 4) Acidic solution Steps Divide into halfreactions, including electrons and oxidation numbers d. Balance all but O and H Balance O by adding H 2 O Balance H by adding H + e. Multiply the halfreactions if necessary so that the electrons will cancel when the two halfreactions are added together f. Remember to always check both mass and charge balance for

3 3 of 13 correctness Examples Cr 2 O 7 2 (aq) + Cl (aq) > Cr 3+ (aq) + Cl 2 (g) (acidic solution) i ii Cr 2 O e > 2 Cr 3+ 2 Cl > Cl 2 (g) + 2 e 14 H + + Cr 2 O e > 2 Cr H 2 O 2 Cl > Cl 2 (g) + 2 e 14 H + + Cr 2 O e > 2 Cr H 2 O 6 Cl > 3 Cl 2 (g) + 6 e 14 H + + Cr 2 O Cl > 2 Cr Cl 2 (g) + 7 H 2 O Cu (s) + NO 3 (aq) > Cu 2+ (aq) + NO 2 (g) (acidic solution) i ii Cu + > Cu e NO 3 (aq) + e > NO 2 Cu + > Cu e 2 H + + NO 3 (aq) + e > NO 2 + H 2 O Cu + > Cu e 4 H NO 3 (aq) + 2 e > 2 NO H 2 O 4 H + + Cu + 2 NO 3 (aq) > Cu NO H 2 O Mn 2+ (aq) + NaBiO 3 (s) > Bi 3+ (aq) + MnO 4 (aq) (acidic solution) i ii Mn 2+ (aq) + > MnO e NaBiO 3 (s) + 2 e > Bi 3+ 4 H 2 O + Mn 2+ (aq) + > MnO e + 8 H + 6 H + + NaBiO 3 (s) + 2 e > Bi H 2 O + Na + 8 H 2 O + 2 Mn 2+ (aq) + > 2 MnO e + 16 H + 30 H NaBiO 3 (s) + 10 e > 5 Bi H 2 O + 5 Na + 2 Mn 2+ (aq) + 5 NaBiO 3 (s) + 14 H + > 2 MnO Bi Na H 2 O C. Basic solution Steps: balance as if in acidic solution, then add equal numbers of OH to each so as to convert any H + to H 2 O

4 4 of 13 Examples CN (aq) + MnO 4 (aq) > CNO (aq) + MnO 2 (s) (basic solution) i ii CN > CNO + 2 e (C is 4+ in each compound) MnO e > MnO 2 H 2 O + CN > CNO + 2 e + 2 H + 4 H + + MnO e > MnO H 2 O 3 H 2 O + 3 CN > 3 CNO + 6 e + 6 H + 8 H MnO e > 2 MnO H 2 O v. 3 CN + 2 MnO H + > 3 CNO + 2 MnO 2 + H 2 O 3 CN + 2 MnO H OH > 3 CNO + 2 MnO 2 + H 2 O + 2 OH v 3 CN + 2 MnO H 2 O > 3 CNO + 2 MnO 2 + H 2 O + 2 OH vi 3 CN + 2 MnO 4 + H 2 O > 3 CNO + 2 MnO OH NO 2 (aq) + Al (s) > NH 3 (aq) + Al(OH) 4 (aq) (basic solution) i ii NO e > NH 3 Al > Al(OH) 4 (aq) + 3 e 7 H + + NO e > NH H 2 O 4 H 2 O + Al > Al(OH) 4 (aq) + 4 H e 7 H + + NO e > NH H 2 O 8 H 2 O + 2 Al > 2 Al(OH) 4 (aq) + 8 H e v. v vi NO Al + 6 H 2 O > NH Al(OH) 4 + H + NO Al + 6 H 2 O + OH > NH Al(OH) 4 + H + + OH NO Al + 6 H 2 O + OH > NH Al(OH) 4 + H 2 O NO Al + 5 H 2 O + OH > NH Al(OH) 4 Cr(OH) 3 (s) + ClO (aq) > CrO 4 2 (aq) + Cl 2 (g) (basic solution) Cr(OH) 3 > CrO e 2 ClO + 2 e > Cl 2 i H 2 O + Cr(OH) 3 > CrO H e

5 of 13 ii 2 ClO + 4 H + + 2 e > Cl 2 + 2 H 2 O 2 H 2 O + 2 Cr(OH) 3 > 2 CrO 4 2 + 10 H + + 6 e 6 ClO + 12 H + + 6 e > 3 Cl 2 + 6 H 2 O 2 Cr(OH) 3 + 6 ClO + 2 H + > 2 CrO 4 2 + 3 Cl 2 (g) + 4 H 2 O v.

5 5 of 13 ii 2 ClO + 4 H e > Cl H 2 O 2 H 2 O + 2 Cr(OH) 3 > 2 CrO H e 6 ClO + 12 H e > 3 Cl H 2 O 2 Cr(OH) ClO + 2 H + > 2 CrO Cl 2 (g) + 4 H 2 O v. v 2 Cr(OH) ClO + 2 H OH > 2 CrO Cl 2 (g) + 4 H 2 O + 2 OH 2 Cr(OH) ClO + 2 H 2 O > 2 CrO Cl 2 (g) + 4 H 2 O + 2 OH vi 2 Cr(OH) ClO > 2 CrO Cl 2 (g) + 2 H 2 O + 2 OH III. Voltaic cells A. Voltaic cells: (also known as galvanic cells) take advantage of the energy released in spontaneous redox reactions to do useful work Batteries, fuel cells Electrolytic cells are devices that use electrical energy from the surroundings to drive nonspontaneous reactions in a system B. Cell structure: a voltaic cell consists of two halfcells that are electrically connected in such a manner that electrons flow from one metal electrode to another through an external pathway A microscopic view of a voltaic cell Two solid metals are connected by an external path (or circuit) and are called electrodes i Anode: oxidation; cathode: reduction Cations move toward the positively charged cathode while

6 of 13 anions move toward the negatively charged anode ii This movement of ions, coupled with the flow of electrons through the external path, completes the circuit A salt bridge connects the two

6 6 of 13 anions move toward the negatively charged anode ii This movement of ions, coupled with the flow of electrons through the external path, completes the circuit A salt bridge connects the two halfcells, permitting the flow of charge and preserving charge balance, but preventing the mixing of the solutions in the halfcells The electrolyte solution in the salt bridge contains ions that will not react with other ions or the electrodes in the halfcells, often KCl or sodium nitrate solutions "Waterfall analogy:" in any voltaic cell electrons flow from the anode through the external circuit to the cathode Just as things located "high" have more gravitational potential energy than things in a "low" position, certain materials have an intrinsically "higher" electrical potential energy than other materials with "lower" electrical potential energies C. Cell notation: shorthand designations of the halfreactions in a voltaic cell Zn (s) Zn 2+ (aq) (1 M) Cu 2+ (aq) (0.1 M) Cu (s) " " indicates a phase boundary, and " " indicates a salt bridge States of materials in the halfcells must be described, and the concentrations of ions in solutions must also be included By cell notation convention the anode is on the left, the cathode is on the right, and the electrodes are the extreme ends of the notation Some halfreactions in voltaic cells involve a gas or two different ions in the same solution H + (aq) (1 M) H 2 (g) (1 atm) Pt (s) Fe 3+ (aq) (1 M), Fe 2+ (aq) (1 M), Pt (s) IV. Electromotive force (emf): the driving force that "pushes" electrons from the anode to the cathode through the external circuit, attributable to differences between the two halfcells A. Standard cell potential (also called the standard emf) depends on the reactions

7 7 of 13 occurring in the halfcells, the concentrations of reactants, and temperature 3. Standard conditions: 1 M concentration for aqueous species, 1 atm pressure for gases, 298 K Under standard conditions emf is called the standard emf and is indicated with the symbol E cell E cell = E red E ox B. E cell depends on the two halfreactions taking place Could empirically determine the values of E cell for all possible halfcell combinations (note: if the number of halfcells is N, then the total possible number of values would be (N 2 N)) Alternatively, could measure all halfcells relative to a standard reference electrode Standard hydrogen electrode: 2 H + (aq) (1 M) + 2 e > H 2 (g) (1 atm) : E red = 0.00 V Standard calomel electrode The set up i Zn (s) + 2 H + (aq) > Zn 2+ (aq) + H 2 (g) The measured cell voltage is 0.76 V ii E cell = E cathode E anode = E red E ox = 0.00 V 0.76 V = 0.76 V Note that whenever a potential is assigned to a halfreaction it is for the reduction reaction, e., the reaction in the halfcell is written as a reduction d. The resulting measured values are found in tables of standard reduction potentials (BLB Table 20.1)

8 8 of 13 C. Standard reduction potentials make it possible to predict both the direction and magnitude of electron flow for a large variety of voltaic cells The more positive (or, the less negative) the value of the standard reduction potentials the greater the driving force for reduction In comparing standard reduction potentials (BLB Table 20.1, see also Appendix E, p. 1128), there is a rough correlation with electronegativity trends, but it is only obviously apparent at the extreme values of the table (Li and F) The more positive the standard reduction potential of a specie, the more powerful it is as an oxidizing agent The more negative the standard reduction potential of a specie, the more powerful it is as an reducing agent d. e. Oxidizing agents oxidize something else and reduce themselves Reducing agents reduce something else and oxidize themselves E red is an intensive property, e. it is independent of quantity

9 9 of 13 Fe 2+ (aq) + 2 e > Fe (s) ; E red = 0.76 V 2 Fe 2+ (aq) + 4 e > 2 Fe (s) ; E red = 0.76 V 3. E cell values are calculated by combining the standard reduction potentials of the two halfcells; if the resulting value of E cell is positive then the reactions in the voltaic cell are spontaneous as written Given two halfcells, Zn Zn 2+ and Cu Cu 2+, which will be the anode? The cathode? What will E cell be? i ii Zn 2+ (aq) + 2 e > Zn (s) ; E red = 0.76 V Cu 2+ (aq) + 2 e > Cu (s) ; E red = V Zn (s) > Zn 2+ (aq) + 2 e ; E ox = V Cu 2+ (aq) + 2 e > Cu (s) ; E red = V Zn (s) + Cu 2+ (aq) > Zn 2+ (aq) + Cu (s) ; E cell = V V = +10 V Given two halfcells, Al Al 3+ and Sn 2+ Sn 4+, which will be the anode? The cathode? What will E cell be? i ii Al 3+ (aq) + 3 e > Al (s) ; E red = 66 V Sn 4+ (aq) + 2 e > Sn 2+ (aq) ; E red = V Al (s) > Al 3+ (aq) + 3 e ; E red = + 66 V Sn 4+ (aq) + 2 e > Sn 2+ (aq) ; E red = V 2 Al (s) > 2 Al 3+ (aq) + 6 e ; E red = + 66 V 3 Sn 4+ (aq) + 6 e > 3 Sn 2+ (aq) ; E red = V 2 Al (s) + 3 Sn 4+ (aq) > 2 Al 3+ (aq) + 3 Sn 2+ (aq); E cell = +66 V V = +81 V What is E cell for the reaction 2 Br(aq) + I 2 (s) > 2 I(aq) + Br 2 (l)? Will it be product favored? i ii Br 2 (l) + 2 e > 2 Br(aq); E red = +07 V I 2 (s) + 2 e > 2 I(aq); E red = V 2 Br(aq) > Br 2 (l) + 2 e ; E red = 07 V I 2 (s) + 2 e > 2 I(aq); E red = V 2 Br(aq) + I 2 (s) > 2 I(aq) + Br 2 (l) ; E cell = 07 V V = 0.53 V; the forward reaction is not favored V. Gibbs free energy, equilibrium, and electromotive force A. E cell is always positive for spontaneous reactions

10 10 of 13 B. The relationship between free energy and E cell is described by the equation ΔG = nfe cell n = number of moles of electrons transferred in the reaction F = Faraday's constant = 96,400 J/V mol ΔG is called the maximum work function, e., it describes the maximum amount of useful electrical work that can be obtained from a voltaic cell For the voltaic cell Zn Zn 2+ Cu 2+ Cu E cell is 10 V. What is ΔG for this cell? ΔG = nfe cell = (2 moles) x (96,400 J/V mol) x (10 V) = 212 kj 5. In the reaction of hydrogen gas and zinc ion H 2 (g) + Zn 2+ (aq) + 2 H 2 O (l) > Zn (s) + 2 H 3 O + (aq) (E cell = 0.76 V), is the reaction spontaneous? Is it product or reactant favored? ΔG = nfe cell = (2 moles) x (96,400 J/V mol) x (0.76 V) = kj Reaction is nonspontaneous and is reactant favored C. Given that at equilibrium ΔG = RT lnk, and also given that ΔG = nfe cell, then +RT lnk = +nfe cell,or E cell = (RT/nF) ln K For the voltaic cell Zn Zn 2+ Cu 2+ Cu E cell is 10 V. What is the equilibrium constant (K c ) for this reaction? K c = exp (nfe cell / RT); assume 298 K K c = 49 x D. How can predictions for nonstandard conditions be made? Derivation d. e. ΔG = ΔG + RT ln Q ΔG = nfe cell nfe cell = ΔG + RT ln Q = nfe cell + RT ln Q E cell = E cell (RT / nf) ln Q (Nernst Equation) If using base 10 logarithms then E cell = E cell V / n log Q Examples Find E cell for a cell in which [Cu 2+ ] = 5.0 M and [Zn 2+ ] = 0.05 M at 298 K.

11 11 of 13 Remember that Zn (s) + Cu 2+ (aq) > Zn 2+ (aq) + Cu (s) and that E cell = 10 V i Q = [Zn 2+ ] / [Cu 2+ ] ii E cell = E cell (RT / nf) ln Q = +10 V (8.314 J/mol K x 298 K / 2 x 96,400 J/V mol) ln (.05/5) = 16 V The standard cell potential for the reaction of dichromate ion and iodide in acidic solution at 298 K is 0.79 V. What is E cell if [Cr 2 O 7 2 ] = 0 M, [H + ] = 0 M, [I ] = 0 M, and [Cr 3+ ] = 0 x 10 5? Cr 2 O 7 2 (aq) + 6 I (aq) + 14 H + (aq) > 2 Cr 3+ (aq) + 3 I 2 (s) + 7 H 2 O (l) i Q = [Cr 3+ ] 2 / [Cr 2 O 7 2 ] [H + ] 14 [I ] 6 = 5.0 x ii E cell = E cell (RT / nf) ln Q = V (8.314 J/mol K x 298 K / 6 x 96,400 J/V mol) ln (5.0 x ) = V If the voltage in a Zn H + cell is 0.45 V at 25 C when [Zn 2+ ] = 0 M and P H2 = 0 atm, what is the hydrogen ion concentration? i ii v. v vi Zn (s) + 2 H + (aq) > Zn 2+ (aq) + H 2 (g) (E cell = V, n = 2) E cell = E cell (RT / nf) ln Q E cell E cell = (RT / nf) ln Q (nf/rt)(e cell E cell )= ln Q exp [(nf/rt)(e cell E cell )] = Q = [Zn 2+ ] P H2 /[H + ] 2 [exp [(nf/rt)(e cell E cell )]] 1 = [H + ] 2 / [Zn 2+ ] P H2 [Zn 2+ ] P H2 [exp [(nf/rt)(e cell E cell )]] 1 = [H + ] 2 vii ix. {[Zn 2+ ] P H2 [exp [(nf/rt)(e cell E cell )]] 1}1/2 = [H + ] = 5.78 x 10 6 Relevance: "this shows how a voltaic cell whose cell reaction involves H + can be used to measure [H + ] of ph. a ph meter is a specially designed voltaic cell with a voltmeter calibrated to read ph directly." (BLB: 775) VI. Electrolytic cells use electrical energy to do work in a nonspontaneous chemical system, e., to drive an otherwise nonspontaneous reaction A. Molten salt solutions The extraction of magnesium and chlorine from brine

12 12 of 13 Mg 2+ (aq) + 2 e > Mg (s) ; E red = 37 V Cl 2 (g) + 2 e > 2 Cl (aq) ; E red = +36 V Mg 2+ (aq) + 2 e > Mg (s) ; E red = 37 V 2 Cl (aq) > Cl 2 (g) + 2 e; E ox = 36 V Mg 2+ (aq) + 2 Cl (aq) > Mg (s) +Cl 2 (g) ; E cell = 37 V + 36V = 3.73 V d. Note that ΔG = nfe cell = +719 kj and K c = 8.73 x (!) To drive the reaction a pair of inert (often graphite) electrodes is inserted in the molten salt bath and a power source serves as an "electron pump" Oxidation still occurs at the anode and reduction still occurs at the cathode but the sign conventions are opposite from those for voltaic cells In voltaic cells the () electrode is where electrons are produced B. In electrolytic cells the () electrode is where electrons are "pumped" Aqueous solutions the presence of water potentially complicates things since 2 H 3 O + (aq) + 2 e > 2 H 2 O (l) + H 2 (g) (E cell = 0.00 V) and 2 H 2 O (l) + 2 e > 2 H 2 (g) + OH(aq) (E cell = 0.83 V) are also possible reactions For an aqueous solution of magnesium chloride Possible reduction reactions i ii Mg 2+ (aq) + 2 e > Mg (s) ; E red = 37 V 2 H 3 O + (aq) + 2 e > 2 H 2 O (l) + H 2 (g) ; E cell = 0.00 V 2 H 2 O (l) + 2 e > 2 H 2 (g) + OH(aq); E cell = 0.83 V Possible oxidation reactions i Cl 2 (g) + 2 e > 2 Cl (aq) ; E red = +36 V O 2 (g) + 4 H 3 O + (aq) + 4 e > 6 H 2 O (l) ; E red = +23 V How can we know which reaction will occur? Remember that the

13 13 of 13 more positive the standard reduction potential of the halfreaction, the easier it is to reduce, although concentration effects may also be significant At the cathode the ease of reduction is (iii) > (ii) > (i) i ii Which reduction occurs depends in part on [Mg 2+ ]; when [Mg 2+ ] is large (i) dominates but when [Mg 2+ ] is small (ii) dominates Complications can also occur when currents are large (as in commercial electrolytic cells) and when reactant concentrations are small The dominance of one reduction reaction over another also depends on [Cl] [Chemistry 1220 Index Page] Last Modified 01/05/ :10:38

Oxidation-Reduction Review. Electrochemistry. Oxidation-Reduction Reactions. Oxidation-Reduction Reactions. Sample Problem.

Oxidation-Reduction Review. Electrochemistry. Oxidation-Reduction Reactions. Oxidation-Reduction Reactions. Sample Problem. 1 Electrochemistry Oxidation-Reduction Review Topics Covered Oxidation-reduction reactions Balancing oxidationreduction equations Voltaic cells Cell EMF Spontaneity of redox reactions Batteries Electrolysis