Outline:2/23/07 è è Today: Finish Chapter 16 è Chem Dept Seminar – è CAPA 10 – deadline moved to Mon. Ù Chemical Equilibrium: LeChâtelier’s principle G and K eq relationship
Types of Equilibrium Constants: Lots of different names…. K eq, K H, K sp, K a, K b, K f, K c, K p … All the same idea: Extent of rxn… K eq is a number that describes the ratio of products/reactants…
LeChâtelier’s Principle: A system reacts to change in the direction that minimizes the change. Change in concentrations Change in pressures Change in temperatures Demo
LeChâtelier’s Principle Demo: Which way will the reaction shift when water is added? Co(H 2 O) 6 2+ (aq) + 4Cl CoCl 4 2 (aq) + 6H 2 O Toward reactants!!
LeChâtelier’s Principle Demo: Which way will the reaction shift when it is heated? Toward products!! H > 0 (endothermic) Co(H 2 O) 6 2+ (aq) + 4Cl CoCl 4 2 (aq) + 6H 2 O Co(H 2 O) 6 2+ (aq) + heat CoCl 4 2 (aq)
Practice problem: K eq = [Pb 2+ ][Cl ] 2 More PbCl 2 is added: More H 2 O is added: Solid NaCl is added: Solid KNO 3 is added: PbCl 2(s) Pb 2+ (aq) + 2 Cl (aq) More dissolves More precip. Nothing
One last link to thermodynamics: G = G o + RTlnQ At equilibrium: G = 0 ; Q =K eq 0 = G o + RTlnK eq or G o = RTlnK eq or K eq = e Gº/RT There is a relationship between G o and K eq ! (see CAPA-11)
Example: Use the thermodynamic tables to find K eq for the following rxn: N H 2 2 NH 3 at 298 K G o (kJ/mol) 0 0 G o rxn = 32.9 kJ/mol K eq = e G o /RT = e 32,900/(8.315*298) = Watch units!
Example (non std. temp): Use the thermodynamic tables to find K eq for the following rxn: N H 2 2 NH 3 at 773 K H o (kJ/mol) 0 0 46.1 S o (J/molK) o rxn = 92.2 kJ/mol S o rxn = J/mol K G T rxn = o rxn T S o rxn = 61.5 kJ K eq = e G T /RT = e 61,500/(8.315*773) = 7.0 10 5
Example (non std. temp): Use the thermodynamic tables to find K eq for the following rxn: N H 2 2 NH 3 H o (kJ/mol) 0 0 46.1 S o (J/molK) o rxn = 92.2 kJ/mol S o rxn = J/mol K Exothermic reaction + heat K 773K= 7.0 K 298K=
Example: K eq to G o You can also find G o given K eq N H 2 2 NH 3 at 773 K K eq = 7.0 10 5 G o = RTlnK eq G o = (8.314 J/k mol)(773 K) ln(7.0 10 5 ) =61.5 kJ/mol
Let’s practice some more: CAPA-11: problem #3 CAPA-11: problem #3 Some reaction… calculate K eq from G… at 220 K! K eq = e Gº/RT G T = Hº T Sº K eq = e Hº/RT+ Sº/R
Let’s practice some more: CAPA-11: problem #7 CAPA-11: problem #7 2A B + C If 1.00 atm of A initially, and 0.24 atm of C at equilibrium…whats K eq ? 0.24 atm C means 0.24 atm B at equil. K eq = (0.24)(0.24)/ (1.00 .48) atm C means 0.48 atm A decays
Let’s practice some more: CAPA-11: problems #9 & #10 CAPA-11: problems #9 & #10 A + B C K c = 710 calculate [C]/[B] at equilibrium if: 0.01 M A is added to 0.20 M B What must you do first? K is big: take reactants over to products
Let’s practice some more: CAPA-11: problem #9 CAPA-11: problem #9 A + B C K c = Initial Initial 0.01 x + x x Change x (0.19+x) (0.01 x) Equilibrium K=710 = (0.01 x) / x (0.19+x) x is small… x = 7.41e-5
Let’s practice some more: CAPA-11: problem #10 CAPA-11: problem #10 A + B C K c = e Initial Does reaction quotient change? Dilute everything by 10.0… K=710 = (0.01) / (7.41e-5)(0.19) = (0.001) / (7.41e-6)(0.019) ? Q = 7100 Yes!
Let’s practice some more: CAPA-11: problem #9 CAPA-11: problem #9 A + B C K c = e Initial Towards more reactants… Q > Keq…which way does it go? + x + x x Change (7.41e-6+x) (0.019+x) (0.001 x) Equil Q = 7100
Let’s test out those keypads…
What is the equilibrium expression for: BaS (s) + 2 O 2(g) BaSO 4(s) [O 2 ] 2 2. [BaSO 4 ]/[BaS][O 2 ] 2 3. [BaS][O 2 ] 2 /[BaSO 4 ] 4. 1/[O 2 ] 2 5. None of the above
The K p expression equals for: CO (g) + H 2 O (g) CO 2 (g) + H 2(g) If 4 atm each of CO & H 2 O are put into a container what’s the final pressure of CO ? atm atm 3. 5 atm atm 5. None of the above
Have a great week-end!