1 / 27

Chapter 20

Chapter 20. Electrochemistry. Oxidation States electron bookkeeping * NOT really the charge on the species but a way of describing chemical behavior. Oxidation: Loss of electrons Reduction: Gain of electrons

iona-abbott
Download Presentation

Chapter 20

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Chapter 20 Electrochemistry

  2. Oxidation States electron bookkeeping * NOT really the charge on the species but a way of describing chemical behavior. Oxidation: Loss of electrons Reduction: Gain of electrons Oxidizer: Oxidizes another species, it gets reduced. Also called oxidizing agent or oxidant

  3. Reducing agent or reductant: Reduces another species, gives up electrons, it is oxidized Many reactions are oxidation-reduction (redox) reactions I2O5(s) + 5CO(g) I2(s) + 5CO2(g) 3NO2(g) + H2O(l)  2HNO3(aq) + NO(g) -2 0 +4 -2 +5 -2 +2 -2 +1 +5 -2 +2 -2 +4 -2 +1

  4. Balancing Redox Reactions

  5. The following steps summarize the procedure that we use to balance an oxidation-reduction equation by the method of half-reactions when the reaction occurs in acid solution: • Divide the reaction into two complete half-reactions, one for oxidation and the other for reduction. • Balance each half-reaction • First, balance the elements other than H and O • Next, balance the O atoms by adding H2O. • Then, balance the H atoms by adding H+ • Finally, balance the charge by adding e- to the side with the greater positive charge • Multiply each half-reaction by an integer so that the number of electrons lost in one half-reaction equals the number gained in the other. • Add the two half-reactions and simplify where possible by canceling species appearing on both sides of the equation. • Check the equation to make sure that there are the same number of atoms of each kind and the same total charge on both sides.

  6. Voltaic Cells E released from redox reaction can be used to perform electrical work. anode = electrodes where oxidation occurs cathode = electrode where reduction occurs reduce the cat population

  7. Half Reactions Zn(s) Zn2+ + 2e- Cu2+ + 2e-  Cu(s) Zn electrode  mass because Zn(s) Zn2+ + 2e- Cu electrode  mass because Cu2+ + 2e-  Cu(s)

  8. Zn Cu2+ Zn2+ Cu2+ CuSO4 Cu2+ SO42- Zn2+

  9. Cell EMF Electromotive force E is favorable for e- to flow from anode to cathode e-’s at higher potential E in Zn electrode than in Cu electrode What do you know about E? It tends to dissipate. Lower E state is favorable!

  10. Which reaction at anode? Which reaction at cathode? Won’treact Pt electrode but will conduct e- e- e- e- V.M. Anode (-) (+) Salt bridge Which electrode is (+) ?

  11. For the reaction Flow of e- allows the reaction to occur e- e- e- Cu cathode Zn anode V.M. (-) (+) NO3- Na+ Salt bridge: can’t just build up a charge in the cell, keep neutrality by ions in salt bridge. Solution of ZnSO4 Solution of CuSO4 Zn2+ Cu2+

  12. The Potential Difference between two electrodes is measured in volts 1V = 1J/C (energy/unit charge) Volts = Electrical pressure or electromotive force The driving force for reaction to take place. Potential difference = emf = Ecell = cell voltage Measured in volts

  13. Standard emf = standard cell potential, Ecell Standard conditions: 1M concentration for reactants and products and 1atm pressure when gases are used. *Standard Electrode Potentials Ecell = Eox + Ered

  14. Emf and Free Energy G = free energy Energy produced by a reaction that can be used for work G is a measure of spontaneity G = -nFE

  15. N = number of moles of e-transferred E = emf of cell +E = spontaneous -G = spontaneous

  16. Concentration and Cell EMF EMF we have looked at so far has been at standard condition. i.e. 1 molar solutions ? What if you change concentration A guy named Nernst worked it out for you! G = G0 + RT ln Q Q = reaction quotient like equilibrium expression but not at equilibrium (ion product)

  17. Well! Since G = -nFE -nFE = -nFE0 + RT ln Q Solve for E NOW you can measure E and determine concentration of reactant or product

  18. ? emf of at 25°C [Al3+] = 4.0x10-3M [I-] = 0.010M step 1)what’s E0 Al  Al3+ + 3e- I2 2I- + 2e- step 2)R = 8.314 J/K·mol F = 96,500 n = 6 V +1.66 +0.536 E0 = 2.196 Find values for all variables and constants

  19. Q = [Al3+]2[I-]6 = (4.0x10-3)2(0.010)6 = 1.6x10-17 log Q = -16.8 step 3) Plug and Chug

  20. Equilibrium Constants When E = 0, Q = Kc The cell is no longer active NO NET REACTION Substitute in Nernst Equation at 298K Can calculate Kc from E0 for cell. Just assume equilibrium and replace E with 0 and Q with Kc

  21. amps x seconds = coulombs ex. current 60.0A 4.00x103 s How much Mg can be formed from Mg2+ 1) coulombs = (4.00x103s)(60.0A) = 2.4x105 coulombs

  22. Quantitative Aspects of Electrolysis Fe2+ + 2e- Fe 1 mol of Fe2+ needs 2 mol of e- to make 1 mol Fe 1/2 mol Fe2+ need 1 mol e- to make 1/2 mol Fe

  23. Al3+ + 3e- Al For 1 mol Al to form 1 mol Al3+ it must give up 3 mol e-. For 1/2 mol Al to form 1/2 mol Al3+ it must give up 3/2 mol e-. NOW, Can I measure electron flow? You betcha! e-

More Related