Electrochemistry. Galvanic Cell. Page 1. Applications of Redox
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1 Electrochemistry Applications of Redox Review Oxidation reduction reactions involve a transfer of electrons. OIL- RIG Oxidation Involves Loss Reduction Involves Gain LEO-GER Lose Electrons Oxidation Gain Electrons Reduction Solid lead(ii) sulfide reacts with oxygen in the air at high temperatures to form lead(ii) oxide and sulfur dioxide. Which substance is a reductant (reducing agent) and which is an oxidant (oxidizing agent)? A. PbS, reductant; O 2, oxidant B. PbS, reductant; SO 2, oxidant C. Pb 2+, reductant; S 2- oxidant D. PbS, reductant; no oxidant E. PbS, oxidant; SO 2, reductant Applications Moving electrons is electric current. 8 +MnO Fe Mn Fe +3 +4H 2 O Helps to break the reactions into half reactions. 8 +MnO Mn +2 +4H 2 O 5(Fe +2 Fe +3 + ) In the same mixture it happens without doing useful work, but if separate Connected this way the reaction starts Stops immediately because charge builds up. MnO 4 - Fe +2 Galvanic Cell MnO 4 - Fe +2 Salt Bridge allows current to flow Page 1 1
2 Electricity travels in a complete circuit Instead of a salt bridge Porous Disk MnO - 4 Fe +2 MnO 4 - Fe +2 e- e- e- Anode Reducing Agent Cathode Oxidizing Agent Cell Potential Oxidizing agent pulls the electron. Reducing agent pushes the electron. The push or pull ( driving force ) is called the cell potential E cell Also called the electromotive force (emf) Unit is the volt(v) = 1 joule of work/coulomb of charge Measured with a voltmeter Anode Zn +2 SO M ZnSO Cathode Cl - 1 M HCl H 2 in Standard Hydrogen Electrode This is the reference all other oxidations are compared to Eº = 0 º indicates standard states of 25ºC, 1 atm, 1 M solutions. Cl - 1 M HCl H 2 in Page 2 2
3 Cell Potential Zn(s) + Cu +2 (aq) Zn +2 (aq) + Cu(s) The total cell potential is the sum of the potential at each electrode. Eº cell = Eº Zn Zn +2 + Eº Cu +2 Cu We can look up reduction potentials in a table. One of the reactions must be reversed, so change it sign. Cell Potential Determine the cell potential for a galvanic cell based on the redox reaction. Cu(s) + Fe +3 (aq) Cu +2 (aq) + Fe +2 (aq) Fe +3 (aq) + Fe +2 (aq) Cu +2 (aq)+2 Cu(s) Cu(s) Cu +2 (aq)+2 Eº = 0.77 V Eº = 0.34 V Eº = V 2Fe +3 (aq) + 2 2Fe +2 (aq) Eº = 0.77 V Reduction potential More negative Eº more easily electron is added More easily reduced Better oxidizing agent More positive Eº more easily electron is lost More easily oxidized Better reducing agent Line Notation solid Aqueous Aqueous solid Anode on the left Cathode on the right Single line different phases. Double line porous disk or salt bridge. If all the substances on one side are aqueous, a platinum electrode is indicated. For the last reaction Cu(s) Cu +2 (aq) Fe +2 (aq),fe +3 (aq) Pt(s) Cu 2+ Fe +2 In a galvanic cell, the electrode that acts as a source of electrons to the solution is called the ; the chemical change that occurs at this electrode is called. a. cathode, oxidation b. anode, reduction c. anode, oxidation d. cathode, reduction Page 3 3
4 Under standard conditions, which of the following is the net reaction that occurs in the cell? Cd Cd 2+ Cu 2+ Cu a. Cu 2+ + Cd Cu + Cd 2+ b. Cu + Cd Cu 2+ + Cd 2+ c. Cu 2+ + Cd 2+ Cu + Cd d. Cu + Cd 2+ Cd + Cu 2+ Galvanic Cell The reaction always runs spontaneously in the direction that produced a positive cell potential. Four things for a complete description. 1) Cell Potential 2) Direction of flow 3) Designation of anode and cathode 4) Nature of all the componentselectrodes and ions Practice Completely describe the galvanic cell based on the following half-reactions under standard conditions. MnO Mn H 2 O Eº=1.51 V Fe Fe(s) Eº=0.036V Potential, Work and DG emf = potential (V) = work (J) / Charge(C) E = work done by system / charge E = -w/q Charge is measured in coulombs. -w = q E Faraday = 96,485 C/mol q = nf = moles of x charge/mole w = -qe = -nfe = DG Potential, Work and DG DGº = -nfeº if Eº > 0, then DGº < 0 spontaneous if Eº< 0, then DGº > 0 nonspontaneous In fact, reverse is spontaneous. Calculate DGº for the following reaction: Cu +2 (aq)+ Fe(s) Cu(s)+ Fe +2 (aq) Fe +2 (aq) + Fe(s) Eº = 0.44 V Cu +2 (aq)+2 Cu(s) Eº = 0.34 V Cell Potential and Concentration Qualitatively - Can predict direction of change in E from LeChâtelier. 2Al(s) + 3Mn +2 (aq) 2Al +3 (aq) + 3Mn(s) Predict if E cell will be greater or less than Eº cell if [Al +3 ] = 1.5 M and [Mn +2 ] = 1.0 M if [Al +3 ] = 1.0 M and [Mn +2 ] = 1.5M if [Al +3 ] = 1.5 M and [Mn +2 ] = 1.5 M Page 4 4
5 The Nernst Equation DG = DGº +RTln(Q) -nfe = -nfeº + RTln(Q) E = E º - RT ln(q) nf 2Al(s) + 3Mn +2 (aq) 2Al +3 (aq) + 3Mn(s) Eº = 0.48 V Always have to figure out n by balancing. If concentration can gives voltage, then from voltage we can tell concentration. The Nernst Equation As reactions proceed concentrations of products increase and reactants decrease. Reach equilibrium where Q = K and E cell = 0 0 = Eº - RTln(K) nf Eº = RTln(K) nf nf Eº = ln(k) RT Batteries are Galvanic Cells Car batteries are lead storage batteries. Pb +PbO 2 +H 2 SO 4 PbSO 4 (s) +H 2 O Batteries are Galvanic Cells Dry Cell Zn + NH 4 + +MnO 2 Zn +2 + NH 3 + H 2 O + Mn 2 O 3 Batteries are Galvanic Cells Alkaline Zn +MnO 2 ZnO+ Mn 2 O 3 (in base) Batteries are Galvanic Cells NiCad NiO 2 + Cd + 2H 2 O Cd(OH) 2 +Ni(OH) 2 Page 5 5
6 Corrosion Rusting - spontaneous oxidation. Most structural metals have reduction potentials that are less positive than O 2. Fe Fe Eº= 0.44 V O 2 + 2H 2 O + 4 4OH - Eº= 0.40 V Fe +2 + O 2 + H 2 O Fe 2 O 3 + Reactions happens in two places. Salt speeds up process by increasing conductivity Iron Dissolves- Fe Fe +2 Water Fe 2+ Rust O 2 + 2H 2 O +4 4OH - Fe 2+ + O 2 + 2H 2 O Fe 2 O Preventing Corrosion Coating to keep out air and water. Galvanizing - Putting on a zinc coat Has a lower reduction potential, so it is more easily oxidized. Alloying with metals that form oxide coats. Cathodic Protection - Attaching large pieces of an active metal like magnesium that get oxidized instead. Electrolysis Running a galvanic cell backwards. Put a voltage bigger than the potential and reverse the direction of the redox reaction. Used for electroplating A battery >1.10V Zn 1.0 M Zn M Cu +2 Cu Zn 1.0 M Zn M Cu +2 Cu Anode Cathode Cathode Anode Page 6 6
7 Calculating plating Have to count charge. Measure current I (in amperes) 1 amp = 1 coulomb of charge per second q = I x t q/nf = moles of metal Mass of plated metal How long must 5.00 amp current be applied to produce 15.5 g of Ag from Ag + Calculating plating 1. Current x time = charge 2. Charge Faraday = mole of 3. Mol of to mole of element or compound 4. Mole to grams of compound Or the reverse if you want time to plate Calculate the mass of copper which can be deposited by the passage of 12.0 A for 25.0 min through a solution of copper(ii) sulfate. How long would it take to plate 5.00 g Fe from an aqueous solution of Fe(NO 3 ) 3 at a current of 2.00 A? Other uses Electrolysis of water. Separating mixtures of ions. More positive reduction potential means the reaction proceeds forward. We want the reverse. Most negative reduction potential is easiest to plate out of solution. Know the table Redox 2. Recognized by change in oxidation state. 3. Added acid 4. Use the reduction potential table on the front cover. 5. Redox can replace. (single replacement) Page 7 7
8 6. Combination Oxidizing agent of one element will react with the reducing agent of the same element to produce the free element. I - + IO I 2 + H 2 O 7. Decomposition. a) peroxides to oxides b) Chlorates to chlorides c) Electrolysis into elements. d) carbonates to oxides Examples 1. A piece of solid bismuth is heated strongly in oxygen. 2. A strip or copper metal is added to a concentrated solution of sulfuric acid. 3. Dilute hydrochloric acid is added to a solution of potassium carbonate Hydrogen peroxide solution is added to a solution of iron (II) sulfate. 24. Propanol is burned completely in air. 25. A piece of lithium metal is dropped into a container of nitrogen gas. 26. Chlorine gas is bubbled into a solution of potassium iodide. Examples 5. A stream of chlorine gas is passed through a solution of cold, dilute sodium hydroxide. 6. A solution of tin ( II ) chloride is added to an acidified solution of potassium permanganate 7. A solution of potassium iodide is added to an acidified solution of potassium dichromate Magnesium metal is burned in nitrogen gas. 71. Lead foil is immersed in silver nitrate solution. 72. Magnesium turnings are added to a solution of iron (III) chloride. 73. Pellets of lead are dropped into hot sulfuric acid 74. Powdered Iron is added to a solution of iron(iii) sulfate. A way to remember An Ox anode is where oxidation occurs Red Cat Reduction occurs at cathode Galvanic cell- spontaneous- anode is negative Electrolytic cell- voltage applied to make anode positive 47 Page 8 8
9 A student places a copper electrode in a 1 M solution of CuSO 4 and in another beaker places a silver electrode in a 1 M solution of AgNO 3. A salt bridge composed of Na 2 SO 4 connects the two beakers. The voltage measured across the electrodes is found to be volt. (a) Draw a diagram of this cell. (b) Describe what is happening at the cathode (Include any equations that may be useful.) A student places a copper electrode in a 1 M solution of CuSO 4 and in another beaker places a silver electrode in a 1 M solution of AgNO 3. A salt bridge composed of Na 2 SO 4 connects the two beakers. The voltage measured across the electrodes is found to be volt. (c) Describe what is happening at the anode. (Include any equations that may be useful.) A student places a copper electrode in a 1 M solution of CuSO 4 and in another beaker places a silver electrode in a 1 M solution of AgNO 3. A salt bridge composed of Na 2 SO 4 connects the two beakers. The voltage measured across the electrodes is found to be volt. (d) Write the balanced overall cell equation. (e) Write the standard cell notation. A student places a copper electrode in a 1 M solution of CuSO 4 and in another beaker places a silver electrode in a 1 M solution of AgNO 3. A salt bridge composed of Na 2 SO 4 connects the two beakers. The voltage measured across the electrodes is found to be volt. (f) The student adds 4 M ammonia to the copper sulfate solution, producing the complex ion Cu(NH 3 ) + (aq). The student remeasures the cell potential and discovers the voltage to be 0.88 volt. What is the Cu 2+ (aq) concentration in the cell after the ammonia has been added? Page 9 9
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