5.111 Lecture Summary #25

25.1 5.111 Lecture Summary #25 Oxidation/Reduction Lecture 2 Topics:Electrochemical Cells, Faraday's Law, and the Relationship between Gibbs Free Energy and Cell Potential Chapter 12 OXIDATION/REDUCTION REACTIONS Guidelines for assigning oxidation numbers 1) In free elements, each atom has an oxidation number of zero. Example H2 2) For ions composed of only one atom the oxidation number is equal to the charge on the ion. Thus Li+1 has an oxidation number of +1. Group 1 and group 2 metals have oxidation numbers of +1 and +2, respectively. Aluminum has an oxidation number of +3 in all its compounds. 3) The oxidation number of oxygen in most compounds is -2. However, in peroxides such as H2O2 and O2-2, oxygen has an oxidation state of -1. 4) The oxidation number of hydrogen is +1, except when it is bonded to metals in binary compounds, such as LiH, NaH, CaH2. In these cases, its oxidation number is -1. 5) F has an oxidation number of -1 in all its compounds. Other halogens (Cl, Br, and I) have negative oxidation numbers when they occur as halide ions in compounds (Ex. NaCl). However, when combined with oxygen (oxoacids), they have positive oxidation numbers (Ex. ClO-). 6) In a neutral molecule, the sum of the oxidation numbers of all the atoms must be zero. In a polyatomic ion, the sum of oxidation numbers of all the elements in the ion must be equal to the net charge of the ion. For example NH4+ H is +1 N is _-3 Sum is +1 7) Oxidation numbers do not have to be integers. For example, the oxidation number of oxygen in superoxide O2-1 is _ -½ ___ Examples Li2O PCl5 HNO3 N2O Definitions Oxidation Reduction Oxidizing agent Reducing agent – 25.2 Disproportionation Reaction A reactant element in one oxidation state is both oxidized and reduced. NaClO ⇒ NaClO3 + NaCl in basic solution Write the half reactions and determine the changes in oxidation state. Na+ is a spectator ion so: ClO- ⇒ ClO3- ClO- ⇒ Cl- Balancing Redox Reactions (Ch12.2) A. BALANCE IN ACIDIC SOLUTION Fe2+ + Cr2O72- ⇒ Cr3+ + Fe3+ (1) Write two unbalanced half reactions for oxidized and reduced species. Cr2O72- ⇒ Cr3+ Fe2+ ⇒ Fe3+ (2) Insert coefficients to make the number of atoms of all elements except oxygen and hydrogen equal on the two sides of each equation. Cr2O72- ⇒ Cr3+ Fe2+ ⇒ Fe3+ (3) Add H2O to balance oxygen Cr2O72- ⇒ 2Cr3+ Fe2+ ⇒ Fe3+ (4) Balance hydrogen with H+ Cr2O72- ⇒ Fe2+ ⇒ Fe3+ 2Cr3+ + 7H2O 25.3 (5) Balance the charge by inserting electrons 14H+ + Cr2O72- ⇒ 2Cr3+ + 7H2O Fe2+ ⇒ Fe3+ (6) Multiply the half reactions so that the number of electrons given off in the oxidation equals the number of electrons accepted in the reduction. 6e- + 14H+ + Cr2O72- ⇒ 2Cr3+ + 7H2O Fe2+ ⇒ Fe3+ + e (7) Add half reaction, make appropriate cancellations. 6e- + 14H+ + Cr2O72- + 6Fe2+ ⇒ 2Cr3+ + 7H2O + 6Fe3+ + 6e B. BALANCE IN BASIC SOLUTION (Book has a different approach. You can use either.) Fe2+ + Cr2O72- ⇒ Cr3+ + Fe3+ Follow steps (1-7) to get your answer for acidic solution: 14H+ + Cr2O72- + 6Fe2+ ⇒ 2Cr3+ + 7H2O + 6Fe3+ (8) Then "adjust pH" by adding OH- to both sides to neutralize H+. 14OH- + 14H+ + Cr2O72- + 6Fe2+ ⇒ 2Cr3+ + 7H2O + 6Fe3+ + 14OH OR 14H2O + Cr2O72- + 6Fe2+ ⇒ 2Cr3+ + 7H2O + 6Fe3+ + 14OH CANCEL 7 14H2O + Cr2O72- + 6Fe2+ ⇒ 2Cr3+ + 7H2O + 6Fe3+ + 14OH Thus: 7H2O + Cr2O72- + 6Fe2+ ⇒ 2Cr3+ + 6Fe3+ + 14OH 25.4 Today’s material An Electrochemical Cell is a device in which an electric current (a flow of electrons through a circuit) is either produced by a spontaneous chemical reaction or used to bring about a nonspontaneous reaction. Battery - technically, a battery is a collection of cells joined in a series, so the voltage they produce is the sum of the voltages of each cell. ELECTROCHEMICAL CELL voltmeter eZn (s) electrode Cl- eCu (s) cathode K+ salt bridge SO42- (aq) Zn2+ (aq) Cu2+ (aq) SO42- (aq) 2e- 2e- Zn2+ Zn (s) Zn is oxidized to Zn2+ at anode Zn(s) Zn2+ (aq) + 2e- Cu2+ Cu (s) Cu2+ is reduced to Cu at cathode 2+ Cu (s) Cu (aq) + 2e- Anode (Oxidation) Electrons produced from oxidation flow out of compartment through a wire. Positive charge increases in the compartment due to the production of Zn2+ from Zn0. To maintain neutrality, Cl- flows in through the salt bridge. Cathode (Reduction) Elections entering the compartment are consumed in the reduction of Cu 2+ to Cu0. Positive charge decreases and K+ ions migrate through the salt bridge and enter the cathodic compartment to maintain the charge. 25.5 Overall, the electrochemical cell may be represented by: Zn (s) | Zn2+ (aq) || Cu2+ (aq) |Cu (s) Phase boundaries are represented by "|" The salt bridge is represented by "||" In the above electrochemical cell, Zn is consumed and Cu is deposited in a quantity proportional to the charge passed (Faraday's Law). Example: How much Zn is consumed and how much Cu is deposited if a current of 1.0 A flows for 1.0 hours? Step1. Find how much charge passed though the circuit. Q = magnitude of charge in Coulombs (C) I • current in amperes (A) (amperes = coulombs/second) t time in seconds Q = 1.0 A • 3600 sec = 3600 C Step 2. Find how many moles of electrons this charge is equivalent to. Use Faraday's constant 96,485 C/mol = 1 Faraday (ℑ) 3600 C x 1 mol = 0.0373 moles of electrons 96,485 C Step 3. Calculate the number of moles of Zn consumed and Cu deposited and convert to grams. 0.0373 moles of e- passed x 1 mol Zn consumed x 2 moles of e- passed 65.39 g mol = 1.2 g 0.0373 moles of e- passed x 1 mol Cu deposited x 2 moles of e- passed 63.55 g mol = 1.2 g 25.6 Electrodes (anodes, cathodes) are not always consumed or produced during electrochemical experiments. A Pt electrode, which is inert, can be used. Pt (s) Cu (s) salt bridge Cr3+ (aq) Cr 2+ Cu2+ (aq) (aq) Notation for this type of cell is: Pt (s) | Cr2+ (aq) , Cr3+ (aq) || Cu2+ (aq) | Cu (s) Cr2+ (aq) ⇒ Cr3+ (aq) + eCu2+ (aq) + 2e- ⇒ Cu (s) anode cathode A Hydrogen Electrode constructed with Pt is commonly used. Many reduction potentials are measured against a Standard Hydrogen Electrode (S.H.E). The hydrogen electrode is denoted: H+ (aq) | H2 (g) | Pt (s) when it acts as a cathode (H+ is reduced) and Pt (s) | H2 (g) | H+ (aq) when it acts as an anode (H2 is oxidized). Example of cell using hydrogen electrode. Zn (s) 1 M ZnSO4 Zinc electrode H2 gas at 1atm salt bridge 1M HCl Pt (s) Hydrogen electrode 25.7 Cell Potential (∆E cell)/Cell Voltage/Electromotive Force (emf) and Gibbs Free Energy The flow of electrons arises from a potential difference, ∆E, between the electrodes in the circuit. The overall free energy of the cell is related to the cell potential by ∆Gcell = -nℑ∆Ecell n = number of electrons ℑ = Faraday's constant Standard States and Cell Potentials ∆G°cell = -nℑ∆E°cell ∆E°cell = cell potential (cell voltage) in which products and reactants are in their standard states Units for ∆E is volts. Example - Calculate ∆E°cell for Zn (s) | Zn2+ (aq) || Cu2+ (aq) |Cu (s) anode cathode ∆E°(cell) = standard reduction potential for the couple at cathode minus standard reduction potential for the couple at anode ∆E°(cell) = E°(cathode) - E° (anode) Look up Standard REDUCTION Potentials (E°) in back of book (measured against S.H.E) Zn2+ (aq) + 2e- ⇒ Zn (s) Cu2+ (aq) + 2e- ⇒ Cu (s) E° = -0.7628 volts E° = +0.3402 volts ∆E°(cell) = E°(cathode) - E° (anode) E° (Cu2+/Cu(s)) - E°(Zn2+/Zn(s)) = 0.3402 - (-0.7628 ) = 1.103 volts Is the flow of electrons spontaneous? ∆G°cell = -nℑ∆E°cell So, if ∆E°cell is positive, ∆G°cell will be negative. Is a reaction spontaneous when ∆G° is negative? 25.8 Galvanic Cell is an electrochemical cell in which a spontaneous chemical reaction is used to generate an electric current. Electrolytic Cell uses electrical energy provided by an external circuit to carry out nonspontaneous reactions. Summary Whether the cell operates spontaneously can be determined by ∆Ecell. ((+) = spontaneous) ∆Ecell can be calculated from the Standard Reduction Potentials (E°) of half-cell reactions. Meaning of standard reduction potential E° A large positive E° means the element or compound is easy to reduce ex. F2 (g) + 2e- ⇒ 2F- E°=+2.87 volts (easy to add electrons to F2) positive E°, negative ∆G°, favorable Is F2 a good oxidizing agent? A large positive E° means the oxidized species of the couple is very oxidizing. A large negative E° means the element or compound is hard to reduce ex. Li+1 + e- ⇒ Li (s) E°=-3.045 volts (hard to add electrons to Li+1) negative E°, positive ∆G°, not favorable Is Li+1 a good oxidizing agent? A large negative E° means the reduced species of the couple is very reducing. 25.9 Example: What is ∆E° for the cell reaction: 2Fe3+ (aq) + 2I- (aq) ⇒ 2Fe2+ (aq) + I2 (s)? balanced reaction at the cathode: balanced reaction at the anode: Standard Reduction Potentials are: E°(Fe3+/Fe2+) = +0.770 V E° (I2/I-) = +0.535 V ∆E°(cell) = E°(cathode) - E° (anode) = Is the reaction spontaneous? Which is the better oxidizing agent: Fe3+, I2? Which is the better reducing agent: I-, Fe2+? Question: Vitamin B12 has a large negative reduction potential, so how is it reduced in the body? Vitamin B12 needs to be reduced to be active. Proper functioning of an enzyme that requires vitamin B12 and folic acid is thought to be necessary for preventing heart disease and birth defects. Where do you get vitamin B12 and folic acid in your diet? and how is the vitamin B12 reduced?