Chapter 19 Electrochemistry Mr. Watson HST. Mr. Watson Redox Reactions Oxidation loss of electrons Reduction gain of electrons oxidizing agent substance.

Slides:



Advertisements
Similar presentations
Redox potentials Electrochemistry ICS.
Advertisements

Electrochemistry Applications of Redox.
Chapter 20: Electrochemistry
Electricity from Chemical Reactions
1 Electrochemistry Chapter 18, Electrochemical processes are oxidation-reduction reactions in which: the energy released by a spontaneous reaction.
Chapter 17 Electrochemistry
Elektrokeemia alused.
The Study of the Interchange of Chemical and Electrical Energy
Copyright©2000 by Houghton Mifflin Company. All rights reserved. 1 Electrochemistry The study of the interchange of chemical and electrical energy.
Electrolysis non-spontaneous reaction is caused by the passage of an electric current through a solution.
Electrochemistry 18.1 Balancing Oxidation–Reduction Reactions
Chapter 18 Electrochemistry
Predicting Spontaneous Reactions
1 Electrochemistry Chapter 17 Seneca Valley SHS Voltaic (Galvanic) Cells: Oxidation-Reduction Reactions Oxidation-Reduction Reactions Zn added.
CHEM 160 General Chemistry II Lecture Presentation Electrochemistry December 1, 2004 Chapter 20.
Electrochemistry Lincoln High School Version 1.04
Electrochemistry Electrochemical Cell – an apparatus that uses redox reactions to produce electrical energy. Voltaic Cell – a type of electrochemical cell.
Section 18.1 Electron Transfer Reactions 1.To learn about metal-nonmetal oxidation–reduction reactions 2.To learn to assign oxidation states Objectives.
Electrochemistry Lincoln High School Version 1.03
ELECTROCHEMISTRY CHARGE (Q) – A property of matter which causes it to experience the electromagnetic force COULOMB (C) – The quantity of charge equal to.
Electrochemistry AP Chapter 20. Electrochemistry Electrochemistry relates electricity and chemical reactions. It involves oxidation-reduction reactions.
Chapter 18 Electrochemistry. Chapter 18 Table of Contents Copyright © Cengage Learning. All rights reserved Balancing Oxidation–Reduction Equations.
ELECTROCHEMISTRY Electrochemistry involves the relationship between electrical energy and chemical energy. OXIDATION-REDUCTION REACTIONS SPONTANEOUS REACTIONS.
Electrochemistry Chapter 19.
Electrochemistry Chapter 19 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Redox Reactions and Electrochemistry
Electrochemistry Chapter 19 Electron Transfer Reactions Electron transfer reactions are oxidation- reduction or redox reactions. Results in the generation.
Electrochemistry Applications of Redox. Review l Oxidation reduction reactions involve a transfer of electrons. l OIL- RIG l Oxidation Involves Loss l.
Redox Reactions and Electrochemistry
Electrochemistry Chapter 17.
Electrochemistry. Electrochemical Cells  Electrons are transferred between the particles being oxidized and reduced  Two types –Spontaneous = Voltaic.
Electrochemistry is the study of chemical reactions that produce electrical effects.
Electrochemistry Terminology  Oxidation  Oxidation – A process in which an element attains a more positive oxidation state Na(s)  Na + + e -  Reduction.
Electrochemistry Unit 13. Oxidation-Reduction Reactions Now for a quick review. For the following reaction determine what is oxidized/reduced/reducing.
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.
Electrochemistry Chapter 19 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
CHEM 163 Chapter 21 Spring minute review What is a redox reaction? 2.
 Deals with the relation of the flow of electric current to chemical changes and the conversion of chemical to electrical energy (Electrochemical Cell)
Activity Series lithiumpotassiummagnesiumaluminumzincironnickelleadHYDROGENcoppersilverplatinumgold Oxidizes easily Reduces easily Less active More active.
Electrical and Chemical Energy Interconversion
Preview Lesson Starter Objectives Electrochemical Cells Chapter 20.
Electrochemistry: Oxidation-Reduction Reactions Zn(s) + Cu +2 (aq)  Zn 2+ (aq) + Cu(s) loss of 2e - gaining to 2e - Zinc is oxidized - it goes up in.
Oxidation-Reduction Reactions Chapter 4 and 18. 2Mg (s) + O 2 (g) 2MgO (s) 2Mg 2Mg e - O 2 + 4e - 2O 2- _______ half-reaction (____ e - ) ______________________.
Electrochemistry Chapter 3. 2Mg (s) + O 2 (g) 2MgO (s) 2Mg 2Mg e - O 2 + 4e - 2O 2- Oxidation half-reaction (lose e - ) Reduction half-reaction.
Redox Reactions & Electrochemistry Chapter 19 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
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.
Electrochemistry The Study of the Interchange of Chemical and Electrical Energy.
Copyright©2000 by Houghton Mifflin Company. All rights reserved. 1 Electrochemistry The study of the interchange of chemical and electrical energy.
Section 1 Introduction to Electrochemistry
Electrochemistry The Study of the Interchange of Chemical and Electrical Energy.
ELECTROCHEMISTRY CHARGE (Q) – A property of matter which causes it to experience the electromagnetic force COULOMB (C) – The quantity of charge equal to.
Electrochemistry Part Four. CHEMICAL CHANGE  ELECTRIC CURRENT To obtain a useful current, we separate the oxidizing and reducing agents so that electron.
ELECTROCHEMISTRY Electrochemistry relates electricity and chemical reactions. It involves oxidation-reduction reactions (aka – redox) They are identified.
Electrochemistry The Study of the Interchange of Chemical and Electrical Energy.
Chapter 19: Electrochemistry: Voltaic Cells Generate Electricity which can do electrical work. Voltaic or galvanic cells are devices in which electron.
Chapter There is an important change in how students will get their AP scores. This July, AP scores will only be available online. They will.
1 Electrochemistry Chapter 18 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Electrochemistry Terminology  Oxidation  Oxidation – A process in which an element attains a more positive oxidation state Na(s)  Na + + e -  Reduction.
Electrochemistry f.
ELECTROCHEMISTRY CHEM171 – Lecture Series Four : 2012/01  Redox reactions  Electrochemical cells  Cell potential  Nernst equation  Relationship between.
Electrochemistry Terminology  Oxidation  Oxidation – A process in which an element attains a more positive oxidation state Na(s)  Na + + e -  Reduction.
Electrochemistry.
Dr. Aisha Moubaraki CHEM 202
Redox Reactions and Electrochemistry
Unit 12 Electrochemistry
Electrolysis non-spontaneous reaction is caused by the passage of an electric current through a solution.
Electrochemistry Chapter 19
Presentation transcript:

Chapter 19 Electrochemistry Mr. Watson HST

Mr. Watson Redox Reactions Oxidation loss of electrons Reduction gain of electrons oxidizing agent substance that cause oxidation by being reduced reducing agent substance that cause oxidation by being oxidized

HST Mr. Watson Electrochemistry In the broadest sense, electrochemistry is the study of chemical reactions that produce electrical effects and of the chemical phenomena that are caused by the action of currents or voltages.

HST Mr. Watson Oxidation-Reduction Reactions

HST Mr. Watson Voltaic Cells harnessed chemical reaction which produces an electric current

HST Mr. Watson Voltaic Cells Cells and Cell Reactions Daniel's Cell Zn (s) + Cu +2 (aq) ---> Zn +2 (aq) + Cu (s) oxidation half reaction anodeZn (s) ---> Zn +2 (aq) + 2 e - reduction half reaction cathodeCu +2 (aq) + 2 e - ---> Cu (s)

HST Mr. Watson Voltaic Cells copper electrode dipped into a solution of copper(II) sulfate zinc electrode dipped into a solution of zinc sulfate

HST Mr. Watson Voltaic Cells

HST Mr. Watson Hydrogen Electrode consists of a platinum electrode covered with a fine powder of platinum around which H 2(g) is bubbled. Its potential is defined as zero volts. Hydrogen Half-Cell H 2(g) = 2 H + (aq) + 2 e - reversible reaction

HST Mr. Watson

HST Mr. Watson

HST Mr. Watson Standard Reduction Potentials the potential under standard conditions (25 o C with all ions at 1 M concentrations and all gases at 1 atm pressure) of a half- reaction in which reduction is occurring

HST Mr. Watson Some Standard Reduction Potentials Table 18-1, pg 837 Li + + e - ---> Li v Zn e - ---> Zn-0.763v Fe e - ---> Fe-0.44v 2 H + (aq) + 2 e - ---> H 2(g) 0.00v Cu e - ---> Cu+0.337v O 2(g) + 4 H + (aq) + 4 e - ---> 2 H 2 O (l) v F 2 + 2e - ---> 2 F v

HST Mr. Watson If the reduction of mercury (I) in a voltaic cell is desired, the half reaction is: Which of the following reactions could be used as the anode (oxidation)? A, B

HST Mr. Watson Cell Potential the potential difference, in volts, between the electrodes of an electrochemical cell Direction of Oxidation-Reduction Reactions positive value indicates a spontaneous reaction

HST Mr. Watson Standard Cell Potential the potential difference, in volts, between the electrodes of an electrochemical cell when the all concentrations of all solutes is 1 molar, all the partial pressures of any gases are 1 atm, and the temperature at 25 o C

HST Mr. Watson Cell Diagram the shorthand representation of an electrochemical cell showing the two half- cells connected by a salt bridge or porous barrier, such as: Zn (s) /ZnSO 4(aq) //CuSO 4(aq) /Cu (s) anode cathode

HST Mr. Watson Metal Displacement Reactions solid of more reactive metals will displace ions of a less reactive metal from solution relative reactivity based on potentials of half reactions metals with very different potentials react most vigorously

HST Mr. Watson Ag+ + e- --->Ag E°= 0.80 V Cu e- ---> Cu E°= 0.34 V Will Ag react with Cu 2+ ? yes, no Will Cu react with Ag+? yes, no

HST Mr. Watson Gibbs Free Energy and Cell Potential  G = - nFE wheren => number of electrons changed F => Faraday’s constant E => cell potential

HST Mr. Watson Applications of Electrochemical Cells Batteries – device that converts chemical energy into electricity Primary Cells – non-reversible electrochemical cell – non-rechargeable cell Secondary Cells – reversible electrochemical cell – rechargeable cell

HST Mr. Watson Applications of Electrochemical Cells Batteries Primary Cells "dry" cell & alkaline cell 1.5 v/cell mercury cell 1.34 v/cell fuel cell 1.23v/cell Secondary Cells lead-acid (automobile battery) 2 v/cell NiCad 1.25 v/cell

HST Mr. Watson “Dry” Cell

HST Mr. Watson “Dry” Cell

HST Mr. Watson “Flash Light” Batteries "Dry" Cell Zn (s) + 2 MnO 2(s) + 2 NH > Zn +2 (aq) + 2 MnO(OH) (s) + 2 NH 3 Alkaline Cell Zn (s) + 2 MnO 2(s) ---> ZnO (s) + Mn 2 O 3 (s)

HST Mr. Watson “New” Super Iron Battery Mfe(VI)O 4 + 3/2 Zn 1/2 Fe(III) 2 O 3 + 1/2 ZnO + MZnO 2 (M = K 2 or Ba) Environmentally friendlier than MnO 2 containing batteries.

HST Mr. Watson Mercury Cell

HST Mr. Watson Lead-Acid (Automobile Battery)

HST Mr. Watson Lead-Acid (Automobile Battery) Pb (s) + PbO 2(s) + 2 H 2 SO 4 = 2 PbSO 4(s) + 2 H 2 O 2 v/cell

HST Mr. Watson Nickel-Cadmium (Ni-Cad) Cd (s) + 2 Ni(OH) 3(s) = Cd(OH) 2(s) + 2 Ni(OH) 2(s) NiCad 1.25 v/cell

HST Mr. Watson Hydrogen-Oxygen Fuel Cell

HST Mr. Watson Automobile Oxygen Sensor

HST Mr. Watson Automobile Oxygen Sensor see Oxygen Sensor Movie from Solid-State Resources CD-ROM

HST Mr. Watson pH = (E glass electrode - constant)/ pH Meter

HST Mr. Watson Effect of Concentration on Cell Voltage: The Nernst Equation E cell = E o cell - (RT/nF)ln Q E cell = E o cell - (0.0592/n)log Q whereQ => reaction quotient Q = [products]/[reactants]

HST Mr. Watson EXAMPLE: What is the cell potential for the Daniel's cell when the [Zn +2 ] = 10 [Cu +2 ] ? Q = ([Zn +2 ]/[Cu +2 ] = (10 [Cu +2 ])/[Cu +2 ] = 10 E o = (0.34 V) Cu couple + (-(-0.76 V) Zn couple n = 2, 2 electron changeE cell = E o cell - (0.0257/n)ln Q thusE cell = ( (0.0257/2)ln 10) V E cell = ( (0.0257/2)2.303) V E cell = ( ) V = 1.07 V

HST Mr. Watson Nernst Equation [H + ] acid side  [H + ] base side E = E o – RT nF ln Q = – 2.3 RT F log [H + ] base side [H + ] acid side [h + ] p-type side  [h + ] n-type side E (in volts) = – 2.3 RT F log [h + ] n-type side [h + ] p-type side

HST Mr. Watson Electrolysis non-spontaneous reaction is caused by the passage of an electric current through a solution

HST Mr. Watson Electrolysis of KI (aq)

HST Mr. Watson Electrolysis Electrolysis of Sodium chloride (chlor-alkali process) molten reactants =>liquid sodium and chlorine gas aqueous reactants => caustic soda (sodium hydroxide) and chlorine gas

HST Mr. Watson Aqueous Reactants => caustic soda (sodium hydroxide) and chlorine gas

HST Mr. Watson Molten Reactants => liquid sodium and chlorine gas

HST Mr. Watson Electrolysis Preparation of Aluminum (Hall process)

HST Mr. Watson Electrolytic Refining of Copper Cu (s) + Cu +2 (aq) --> Cu +2 (aq) + Cu (s) impure pure anode cathode impurities: anode mud; Ag, Au, Pb

HST Mr. Watson Copper Purification

HST Mr. Watson Copper Purification

HST Mr. Watson Hall Process for Aluminum

HST Mr. Watson Quantitative Aspects of Electrolysis 1 coulomb = 1 amp sec 1 mole e - = 96,500 coulombs

HST Mr. Watson Electroplating EXAMPLE: How many grams of chromium can be plated from a Cr +6 solution in 45 minutes at a 25 amp current?

HST Mr. Watson Electroplating EXAMPLE: How many grams of chromium can be plated from a Cr +6 solution in 45 minutes at a 25 amp current? (45 min) #g Cr =

HST Mr. Watson Electroplating EXAMPLE: How many grams of chromium can be plated from a Cr +6 solution in 45 minutes at a 25 amp current? definition of minute (45 min)(60 sec) #g Cr = (1 min)

HST Mr. Watson Electroplating EXAMPLE: How many grams of chromium can be plated from a Cr +6 solution in 45 minutes at a 25 amp current? (45) (60 sec) (25 amp) #g Cr = (1)

HST Mr. Watson Electroplating EXAMPLE: How many grams of chromium can be plated from a Cr +6 solution in 45 minutes at a 25 amp current? definition of a coulomb (45)(60 sec)(25 amp)(1 C) #g Cr = (1) (1 amp sec)

HST Mr. Watson Electroplating EXAMPLE: How many grams of chromium can be plated from a Cr +6 solution in 45 minutes at a 25 amp current? Faraday’s constant (45)(25)(60)(1 C)(1 mol e - ) #g Cr = (1)(1)(96,500 C)

HST Mr. Watson Electroplating EXAMPLE: How many grams of chromium can be plated from a Cr +6 solution in 45 minutes at a 25 amp current? atomic weight (45)(60)(25)(1)(1 mol e - )(52 g Cr) #g Cr = (1)(1)(96,500) (6 mol e - )

HST Mr. Watson Electroplating EXAMPLE: How many grams of chromium can be plated from a Cr +6 solution in 45 minutes at a 25 amp current? (45)(60)(25)(1)(1 mol e - )(52 g Cr) #g Cr = (1)(1)(96,500)(6 mol e - ) = 58 g Cr

HST Mr. Watson Rusting of Iron

HST Mr. Watson Corrosion O 2(g) + 4 H + (aq) + 4 e > 2 H 2 O (l) E o = 1.23 V Rusting Fe (s) -----> Fe +2 (aq) + 2 e - E o = 0.44 V O 2(g) + 4 H + (aq) + 4 e > 2 H 2 O (l) E o = 1.23 V Fe (s) + O 2(g) + 4 H + (aq) -----> 2 H 2 O (l) + Fe +2 (aq) E o = 1.67 V

HST Mr. Watson Preventing Corrosion painting galvanizing sacrificial anode