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0. NH + 4 (aq) + H O(l) H 3 O + (aq) + NH 3 (aq) unbuffered 0.35 x 0.35 [H K a 3 O + ][NH 3 ] [NH + x(0.35) 5.6 10 10 4 ] 0.35 x 5.6 10 10 ph log 5.6 10 10 9.5 NH + 4 (aq) + H O(l) H 3 O + (aq) + NH 3 (aq) buffered 0.45 x 0.5 [H K a 3 O + ][NH 3 ] [NH + x(0.5) 5.6 10 10 4 ] 0.45 x 1.0 10 10 ph log 1.0 10 10 9.00 The ph would change from 9.6 to 9.00, which shows the buffering effect of the system..1 10 3 g 1. n(mgf ) 3.40 10 5 6.31 g/ [MgF ] 3.40 10 5.7 10 4 / 0.15 MgF (s) Mg + (aq) + F (aq).7 10 4 (.7 10 4 ) K sp [Mg + ][F ] (.7 10 4 )(5.44 10 4 ) 8.05 10 11. a. The ph range is from 4.5 to 5. b. These ended up being good choices for this unknown solution, as it narrowed the ph to a relatively small range. If the unknown was a base or outside this ph range, the choice would not have been a good one. 3. Hemoglobin HHb(aq), and the oxygenated form oxyhemoglobin, HbOO (aq) react as follows: HHb(aq) + O (g) + H O(l) H 3 O + (aq) + HbOO (aq) Because the hydronium ions are part of this equilibrium process, the ph of the blood plays a critical role in the ability of hemoglobin to combine with oxygen. If the blood ph becomes too acidic, the equilibrium will shift to the left, which will cause the hemoglobin to lose the ability to combine with the oxygen. If the blood ph becomes too basic, the hemoglobin will attach to more and more oxygen, but then loses its ability to release the oxygen when it reaches the cell site that is in need of the oxygen. Blood ph must remain as close to 7.4 as possible to have a balance of oxygen pick up and release in the body. 4. n(ce 3+ ) cv 4.0 10 3 / 0.75000 3.000 10 3 [Ce 3+ ] 3.000 10 3.857 10 3 / 1.050 n(io 3 ) cv.0 10 / 0.30000 6.0000 10 3 [IO 3 ] 6.0000 10 3 5.714 10 3 / 1.050 Q sp [Ce 3+ ][IO 3 ] 3 (.857 10 3 )(5.714 10 3 ) 3 5.33 10 10 Since Q sp 5.3 10 10, which is larger than K sp for the solid, a precipitate will form..17 10 g 5. n(ag CrO 4 ) 6.54 10 5 331.74 g/ [Ag CrO 4 ] 6.54 10 5 / Ag CrO 4 (s) Ag + (aq) + CrO 4 (aq) (6.54 10 5 ) 6.54 10 5 K sp [Ag + ] [CrO 4 ] [(6.54 10 5 )] (6.54 10 5 ) 1.1 10 1 Answers to Unit 4 Review Questions (Student textbook pages 569-73) 1. a. e 3. d 4. a 5. c 6. b 7. e 8. a 9. e 10. b 11. a. K eq [CO ] [HCl] b. K eq [Cl ][HI] 1 c. K eq [HCl][NH 3 ] [H d. K eq O][Cl ] [HCl] [O ] ½ 1. a. CH 3 COO - (aq) and CH 3 COOH(aq); HSO 3 - (aq) and SO 3 - (aq) b. CN - (aq) and HCN(aq); H O(l) and OH - (aq) c. HSO 4 - (aq) and SO 4 - (aq); HCO 3 - (aq) and H CO 3 (aq) d. CH 3 COOH(aq) and CH 3 COO - (aq); HPO 4 - (aq) and H PO 4 - (aq) 13. Since HNO (aq) is a stronger acid than HSO 4 - (aq), the reaction will progress toward the stronger acid, therefore, the reverse reaction is favoured. MHR 37

14. a. HCN(aq) + H O(l) H 3 O + (aq) + CN - (aq) K a [H 3 O + ][CN - ] [HCN] b. NH 3 (aq) + H O(l) H 3 O + (aq) + NH - (aq) K a [H 3O + ][NH - ] [NH 3 ] c. HSO 4 - (aq) + H O(l) H 3 O + (aq) + SO 4 - (aq) K a [H 3O + ][SO 4 - ] [HSO 4 - ] 15. As written the reaction is exothermic, as heat is given off in the process. The K eq value will decrease as the system will shift to the left, decreasing the concentration of products (i.e., the numerator) while increasing the concentrations of reactions (i.e., the denominator), causing the value of the fraction to decrease. 16. Since pressure is being applied to the closed system, the reaction will shift to the left (a side that has fewer es of gas ecules) 17. The structure of carbon monoxide is so similar that of oxygen that carbon monoxide is able to bind to the protein hemoglobin, which normally carries oxygen in the blood. The equilibrium constant for the reaction of hemoglobin with carbon monoxide is much larger than the equilibrium constant for the reaction with oxygen. Due to the fact that hemoglobin binds more readily with carbon monoxide than with oxygen, breathing even small concentrations of carbon monoxide can be a problem. Arterial blood pumped from the heart to the cells and organs would carry too little oxygen, and so the cells would not get enough oxygen to carry out their life processes. 18. Dissociation refers to the breaking of chemical bonds without looking at whether the result is ions in solution or neutral fragments of the original material. However, ionization refers to the process where ions are formed, usually by the actions of solvent ecules. Weak acids and bases dissociate and ionize, but strong acids and bases simply ionize. 19. NH 3 can be amphiprotic as it can form NH 4 + or NH - ; HSO 4 - can be amphiprotic as it can form H SO 4 or SO 4 - ; H PO 4 - can be amphiprotic as it can form HPO 4 - or H 3 PO 4. Other possibilities also exist. 0. a. Syngas is the name given to the mixture of carbon monoxide and hydrogen gas obtained from the methane in natural gas. b. Syngas it the source of hydrogen gas used in the Haber-Bosch process c. When syngas is passed over a catalyst at a pressure of 5 to 10 MPa and a temperature of approximately 50 C, methanol and heat form. 1. All pure liquids have a constant concentration, and so there is no need to include the value in the equilibrium constant expression that monitors how concentrations change.. a. The reverse direction will be favoured as 9 es of gas on the reactant side of the equation take up less space than 10 es of gas that are on the product side. b. Adding a reactant will favour the formation of product, so equilibrium will shift to the right. c. Adding product will favour the formation of reactants, so equilibrium will shift to the left. d. Adding an inert gas will have no effect on the position of equilibrium. e. Increasing the total volume will favour the reaction that takes up more space, so the forward reaction will be favoured. 3. addition of PCl 3 (g); addition of Cl (g); increased pressure; decreased volume; remove PCl 5 (g) as it forms 4. [A ] [B ] [AB] I 1.00 1.00 0 C -x -x +x.5 10 E 1.00 - x 1.00 - x.5 10 x.5 10 x 1.15 10 1.00 - x 1.00 - (1.15 10 ) 1.00 - x 0.9875 Equilibrium concentrations: [A ] 0.9875 / [B ] 0.9875 / [AB].5 10 / [AB] K eq [A][B] (.5 10 ) (0.9875)(0.9875) 6.4 10 4 5. ph log [H 3 O + ] [H 3 O + ] 10 ph [H 3 O + ] 10 4.15 [H 3 O + ] 7.08 10 5 38 MHR

6. percent dissociation I.34.00 [HA] dissociated [HA] initial (7.08 10 5 ) 0.100 0.0708% 0.071% 100% 100% [CO ] [H ] [CO] [H O] 1.17.34.00 1.17 0 0 C -x -x x x E 1.17 - x 1.17 - x x x K eq [CO][H O] [CO ][H ] 1.9 1.9 1.9 1.113578 x x (1.17 - x)(1.17 - x) x (1.17 - x) x (1.17 - x) x 1.17 - x 1.113578(1.17 - x) x 1.388-1.113578x x.113578x 1.388 x 0.687 x 0.69 7. Moles of NH 3 in the solution: n cv 0.100 30.00 m 3.00 10 3 NH 3 1 1000 m Therefore, 3.00 10 3 HCl must be added to reach the equivalence point. Volume HCl added: n cv V n c 3.00 10 3 0.100 0.0300 1000 1 30.0 m Total volume of solution: 30.00 m + 30.00 m 60.00 m Concentration of NH 4 Cl: c 3.00 10 3 1000 m 60.00 m 1 5.00 10 [NH 4 + ] [H O] [NH 3 ] [H 3 O + ] I 5.000 10 0.00 0.000 C -x +x +x E (5.000 10 ) - x x x K a [NH 3][H 3 O + ] [NH + 4 ] 5.6 10 10 x 0.05000 - x (5.6 10 10 )(0.05000 - x) x (.8 10 11 )(5.6 10 10 x) x x + (5.6 10 10 x) - (.8 10 11 ) 0 x -b ± b - 4ac a x -5.6 10 10 ± (5.6 10 10 ) - 4(1)(.8 10 11 ) 1-5.6 10 10 ± 1.0583 10 5 ±5.91 10 6 A concentration cannot be negative so use the positive value. [H 3 O + ] 5.91 10 6 / ph log [H 3 O + ] log (5.91 10 6 ) 5.7 ph 5.7 8. a. shift to the left b. shift to the right c. shift to the left d. no change e. no change, but equilibrium would be established quicker 9. If possible, one or more of the products could be removed or added, without opening the system to the environment (i.e., through injection by syringe), and if there is a change in the system, it was at equilibrium. Otherwise, if there was a difference in the number MHR 39

of es of gas in the system, affecting a pressure or volume change would allow for an equilibrium system to react to this change. If any of these are applied and there is no change to the system, it was a reaction that had gone to completion. 30. Change 1: increase the heat added to the system 31. Change : add more H O(g) to the system Change 3: remove H (g) or O (g), or remove both Change 4: decrease pressure by increasing the total volume of the container. [H ] [Cl ] [HCl] I.00.00 0.00 C -x -x +x E.00 - x.00 - x x [HCl] K eq [H ][Cl ] (x) 50.00 (.00 - x)(.00 - x) 4x 50.00 4.00-4x + x 50.00 (4.00-4x + x ) 4x 00.00-00.0x + 50.00x 4x 46.00x - 00.0x + 00.0 0 x -b ± b - 4ac a 00.0 ± 00.0-4(46.00)(00.0) (46.00) 00 ± 56.5685 9.00.7887 or 1.559 The value.7887 cannot be used because it would make the equilibrium value of the reactants negative numbers. Use 1.559. [HCl] x [HCl] (1.559) 3.118 [HCl] 3.1 3. [NH 3 ] [N ] [H ] I 1.00 0.00 0.00 C -x +x +3x E 1.00 - x x 3x K eq [N ][H ] 3 [NH 3 ] 4. 10 3 4. 10 3 x(3x) 3 (1.00 - x) 7x 4 (1.00 - x) 7 x 4 (1.00 - x) 6.4807 10 5.196x 1.00 - x 6.4807 10-0.1961x 5.196x 5.196x + 0.1961x - 6.4807 10 0 x 0.1961 ± 0.1961-4(5.196)( 6.4807 10 ) (5.196) 0.1961 ± 1.1678 10.39 The negative value cannot be used so use only the positive. x 0.099 x 0.100 [H ] 3x [H ] 3(0.100) [H ] 0.300 The answer can be given in es because the reaction took place in a 1 container. 33. Many possibilities exist, but all reports should include the detailed information of the chemistry of the equilibrium in their chosen system. 34. Many possible answers exist, but most students will choose to use a titration with a strong base to the equivalence point and a ph meter. At the equivalence point for a strong acid, the ph will be 7.00, but for a weak acid, the ph will be larger than 7.00. 35. a. Moles of HOCl: n HOCl cv 0.100 0.00500 5.00 m Moles of ioh at 10.00 m: 3.00 10 3 NH 3 n ioh cv 0.100 0.001000 10.00 m 1 1000 m 1 1000 m HOCl(aq) + ioh(aq) iocl(aq) +H O(l) 40 MHR

[HOCl] [ioh] [iocl] I () 0.00500 0.001000 0.0000 C () -0.001000-0.001000 +0.001000 E () 0.001500 0.0000 0.001000 HOCl(aq) + H O(l) H 3 O + (aq) + OCl K eq 4.0 10 8 K eq 4.0 10 8 [H 3 O + ][OCl ] [HOCl] [H 3 O + ] 0.00100 0.035 0.00150 0.035 [H 3 O + ] (4.0 10 8 )(0.001500) 0.00100 [H 3 O + 8 ] 6.0 10 ph log [H 3 O + ] log 6.0 10 8 7. b. At the equivalence point, enough ioh has been added to convert all of the HOCl to i + + OCl. Therefore, the concentration of the OCl ions is: 0.00500 c OCl 0.035 0.071486 The OCl acts as a weak base and the reaction with water is: OCl (aq) + H O(l) HOCl(aq) + OH (aq) K b.5 10 7 1000 K b.5 10 4 << 0.071486 / so use the approximation [OCl ] [OH ] [HOCl] I 0.071486 0.00 0.00 C -x +x +x E 0.071486 x x K b.5 10 7 [HOCl][OH ] [OCl ] (x)(x) (0.071486).5 10 7 (0.071486) x 1.7857 10 8 x x 1.3363 10 4 [OH ] x [OH ] 1.3363 10 4 poh log [OH ] log 1.3363 10 4 3.8741 ph 14.0 - poh 14.0-3.8741 10.16 10.13 36. AgNO 3 (aq) + Na CrO 4 (aq) Ag CrO 4 (s) + NaNO 3 (aq) Moles of Ag + : n AgNO3 m M 0.74 g g 169.88 4.356 10 3 n Ag + 4.356 10 3 Concentration of Ag + : c n V 4.356 10 3 1.75 [Ag + 3 ].4891 10 Moles of CrO 4 : n Na CrO 4 m M 0.7 g g 161.98 1.6669 10 3 n CrO4 1.6669 10 3 Concentration of CrO 4 : c n V 1.6669 10 3 1.75 [CrO 4 4 ] 9.55 10 Q sp [Ag + ] [CrO 4 ] (.4891 10 3 ) (9.515 10 4 ) 5.90 10-9 Q sp 5.9 10-9, which exceeds the actual K sp value, so a solid will form. MHR 41

37. If the sodium iodide concentration is kept between 8. 10-11 / and 1.7 10-6 /, any precipitate that forms will be the lesser soluble solid, silver iodide. Therefore, any solid that forms when the sodium iodide solution is diluted to this value and added will indicate the presence of silver ions. If there is no precipitate, then there were no silver ions. When the concentration of sodium iodide in solution reaches 1.7 10-6 /, any remaining silver ions will only be present in a concentration of 1 10-11 /, too small a value for any additional solid to precipitate out of solution. Now, if a larger concentration of sodium iodide is added, any solid that forms will be due to the presence of copper(i) ions in solution. 38. At the equivalence point, the number of es of H 3 O + must equal the number of es of OH. Therefore, the number of es of HCl must equal the number of es of NaOH. n HCl n NaOH c HCl V HCl c NaOH V NaOH 0.5 V NaOH (3.00 m) 0.185 0.5 V NaOH 38.9189 m V NaOH 38.9 m 0.185 (3.00 m) V NaOH 39. In a solution of MgCO 3, the number of Mg ions is equal to the number of ions of CO 3. Therefore, when calculating the K sp, you can call the concentration of each of the ions, x. K sp [Mg + ][CO 3 ] 6.8 10 6 (x)(x) x x.6115 10 3 [Mg + ] [CO 3 ] [MgCO 3 ].6115 10 3 m nm cvm.6115 10 3 0.1101 g 0.110 g (0.500 ) 84.3 g 40. a. a strong base such as NaOH(aq) and an indicator such as methyl red or bromocresol green b. the ph range will be from 4 to 6 c. a ph meter can be used to verify the prediction. 41. HNO 3 (aq) + NH 3 (aq) NH 4 + (aq) + NO 3 (aq) Moles of ammonia: n NH4 + c NH4 + V NH4 + 0.100 (5.00 m) 1 1000 m.50 10 3 At the equivalence point, there are equiar amounts of HNO 3 and NH 3 in the solution. n HNO3 n NH3 0.00 c HNO3 V HNO3 c NH3 V NH3 V HNO 3 0.100 (5.00 m) 0.100 (5.00 m) V HNO3 0.00 V HNO3 1.5 m The total volume is now 5.00 m + 1.5 m 37.5 m. The ammonium ion is a weak acid. K a 5.6 10 10 NH 4 + (aq) + H O(l) NH 3 (aq) + H 3 O + (aq) The concentration of the ammonia is: [NH 3 + ].5 10 3 37.5 m 0.06666 1000 m 1 [NH 3 ] [H 3 O + ] [NH 4 + ] I 0.06666 0.00 0.00 C -x +x +x E 0.06666 - x 0.0666 x x 1000 K a 5.6 10 7 >> 0.06666 / so the approximation is valid. K a [H 3O + ][NH 3 ] [NH 4 + ] 5.6 10 10 (x)(x) (0.06666) (0.06666)(5.6 10 10 ) x 3.7333 10-11 x x 6.1101 10 6 4 MHR

[H 3 O + ] 6.1101 10 6 ph log [H 3 O + ] log(6.1101 10 6 ) ( 5.14) 5.1 4. Determine the ar concentration of by dividing by the ar mass of if: g 1.11 c g 5.94 0.0479 K sp [i + ][F ] 0.4379 0.00183 1.83 10 3 0.4379 43. Pb(NO 3 ) (aq) + KCl(aq) PbCl (s) + KNO 3 (aq) Concentration of Pb + after mixing: c i V i c f V f.50 10 3 c f.50 10 3 (15.00 m) c f (5.00 m) (5.00 m) (15.00 m) c f 1.50 10 3 Concentration of Cl after mixing: c i V i c f V f.10 10 c f.10 10 (10.00 m) c f (5.00 m) (5.00 m) c f 8.40 10 3 Q sp [Pb + ][Cl ] (10.00 m) (1.5 10 3 )(8.40 10 3 ) 1.058 10 7 Q sp 1.06 10 7 < K sp 1.7 10 5 so no precipitate will form. 44. Is there a coloured gas in the mixture? Is there a change in the number of es of gas from reactants to products? Is an acid either forming or being used up in the process? Can temperature or concentrations easily be monitored? 45. Students should include the following concepts in their paragraph: reversible reaction; closed system, meaning closed to the environment such that there is no ability for materials to come into or escape the system; no change to a physical observable property in the system; constant temperature. 46. Both have product concentrations in the numerator and reactant concentrations in the denominator. Both use the balanced coefficients as exponents on the reactant and product concentrations. Homogeneous equilibrium constants have all materials in the gas phase, and so all are part of the constant. Heterogeneous equilibrium constants involve some materials that are pure liquids or solids, and these materials have constant concentrations and are left out of the equilibrium constant expressions. 47. When a system is composed of gases, using partial pressures to find a K p value is often easier. This is due to the fact that partial pressures are often more easily measured for gases than ar volumes and concentrations. As long as each gas behaves like an ideal gas, the ideal gas law can be used to find the pressures (or ar volumes if the pressures are known or measured). 48. The choice of graphic organizer will vary, but all choices must include situations such as solving using the quadratic formula, solving by factoring and solving by taking the square root of each side, as well as when each can be used. 49. Student responses will depend on the choice of representation used to illustrate the reaction, but clearly the reaction should illustrate the movement of protons in the reaction between conjugate aid-base pairs. 50. Two possibilities exist: The student can find the poh and then use 14 - poh ph or they can use [H 3 O + (aq)] 1 10-14 to first find the hydronium ion [OH - (aq)] concentrate and then find the ph. 51. Sample answer: A weak acid does not fully dissociate into ions in water, regardless of the amount of acid in solution, whereas a dilute acid simply refers to a low number of es of acid that is in solution, in either ionic or ecular form. MHR 43

5. If the acid dissociation constant is very small, the ecular weak acid does not release high concentrations of ions into solution. As a result, the percent dissociation would be very low. 53. Sample Procedure: 1. Use 10 -ph to determine the equilibrium concentration of the hydronium ion (this will also be the equilibrium concentration of the conjugate base of the weak acid). Subtract this value from the initial concentration of the weak acid. 3. Use the concentrations found in steps 1 and to determine the acid dissociation constant for the weak acid. 4. Divide the hydronium ion concentration by the equilibrium concentration of the weak acid and multiply by 100 to determine the percent dissociation. 54. The student choice of graphic organizer will differ, but items such as finding equivalence points using strong acids and bases, indicators and ph meters should all be considered in the organizer. 55. The table should show: Similarities: both do not fully ionize when they dissociate; both are equilibrium systems with equilibrium constants describing the equilibrium mathematically; both are made up of conjugate acid-base pairs; Differences: ph, colour of the indicator placed in each solution, the weak acid donates a proton to solution while the weak base accepts a proton from solution. 56. An acid-base indicator is a weak acid. HInd is the acid form of the indicator and Ind is the conjugate base form. HInd(aq) + H O(l) H 3 O + (aq) + Ind (aq) The indicator will change colour over a range of ph values, as the two colours overlap in this interval. It is only when the equilibrium is shifted well in either direction that one colour dominates over the other and that colour is seen. 57. The tank is only at equilibrium once the tank is no longer being filled. Once propane is no longer being added and the cylinder is sealed, it will be closed system that is at equilibrium, with the gas forming a liquid at the same time and the same rate as the liquid forms the gas. 58. The reaction could have simply gone to completion and thus no more changes can be seen 59. a. 4NH 3 (g) + 5O (g) 4NO(g) + 6H O(g) K eq [NO]4 [H O] 6 [NH 3 ] 4 [O ] 5 b. Cl (g) + HI(g) I (s) + HCl(g) K eq [HCl] [Cl ][HI] c. NO (g) N O 4 (g) K eq [N O 4 ] [NO ] d. CO(g) + Cl (g) COCl (g) K eq [COCl ] [CO][Cl ] 60. At higher temperatures, it would be expected that more water ecule collisions will cause ionization than at lower temperatures, as higher temperatures indicate more kinetic energy in the ecules. As a result, it would be expected that the K w value would increase at the temperature increases. 61. The system is not at equilibrium, as there will be more collisions forming product ecules. The system will adjust to reach equilibrium again once the rate of the two reactions balances again. 6. As medication is used by the body, the concentration of the medication in the bloodstream decreases. To favour the forward process of the body getting better, it is essential to add more reactant, which would be the medication, to increase its concentration and force the system to move in the forward direction. 63. Many possible examples exist, but the most common would be a rust inhibitor that is designed to remove contact (or at least decrease the contact) between a metal and the environment such as that found on a car door. The idea is to separate the reactants (i.e., the oxygen, iron and moisture) so the process cannot occur as rapidly as it would without the inhibitor. Other students may comment on anti-aging medications that slow down the production of free radicals that cause tissue to lose elasticity and appear aged. 64. K eq 1.15 [H O] [C] [H ] [CO] I 0.500 / 0.500 / 0.00 0.000 C -x -x +x +x E 0.500 - x 0.500 - x x x K eq [H ][CO] [H O][C] (x)(x) 1.15 (0.500 - x)(0.500 - x) 44 MHR

1.15 1.15 x (0.500 - x) x (0.500 - x) x 1.0738 0.500 - x 1.0738(0.500 - x) x 0.53619-1.0738x x.0738x 0.53619 x 0.53619.0738 x 0.5873 [H ] 0.5873 n cv n 0.5873 n 0.51746 n 0.517 65. K eq 0.0400 ( ) [HI] [H ] [I ] I 0.00 / 0.00 0.000 C -x +x +x E.00 - x x x K eq [H ][I ] [HI] 0.0400 0.0400 0.0400 0.00 (x)(x) (.00 - x) x (.00 - x) x.00 - x 0.00(.00 - x) x 0.400-0.00x x 0.400 1.00x x 0.400 1.00 x 0.3333 [H ] 0.3333 x (.00 - x) Because the volume is 1.00, the amount of H gas in the container is: 0.333. 66. ow temperatures may increase the percent yield, but the time needed for the reaction to form enough acid to make it useful would be too long at this temperature. This means that a higher than optimal temperature is used so that the sulfuric acid production is cost effective as a business. 67. The Brønsted-owry theory says compounds or ions act as bases because they are combining with hydrogen ions. The reason they are combining with hydrogen ions is that they have lone pairs of electrons - which is what the ewis theory says. The two theories are consistent. 68. Due to the fact that in the auto-ionization of water, only 1 in 55 million water ecules ionize, even the weakest acids and bases will contribute far more hydroxide and hydronium ions to solution that the contribution due to water ionization does not affect the overall calculations. Even if this was factored in to the calculations, the ph and poh values would be the same as if the auto-ionization of water was not included. Answers to Unit 4 Self-Assessment Questions (Student textbook pages 574-5) 1. b. d 3. K eq [H ][Cl ] [HCl] (4.16 10 4 )(6.37 10 ) (.34 10 ) 0.04839 The answer is a. 4. K eq 5. c 6. d 7. e 8. d [A ][B ] [AB] (0.5)(0.5) (0.50) 0.5 The answer is b. 9. K a K b 10 14 K b 10 14 K a 10 14 7. 10 9 MHR 45

10. a 1.3889 10 6 1.4 10 6 The answer is b. 11. ph log [H 3 O + ] 3.17 log [H 3 O + ] [H 3 O + ] 10 3.17 [H 3 O + ] 6.7608 10 4 [H K a 3 O + ][A ] HA (6.7608 10 K a 4 )(6.7608 10 4 ) 0.150 K a 3.047 10-6 K a 3.05 10-6 1. K eq for reaction 1 will be equal to the square of that written from the second reaction. 13. Pressure will increase until equilibrium is approached. 14. The conclusion is not valid, as the system could simply have a ratio of products to reactants in the gas phase that is the same, which means that the reaction could be at equilibrium and is just not affected by changes in pressure or volume. 15. It is assumed that the inert gas acts like an ideal gas where the particles are considered to take up no volume. Since this is the case, there is no change to the system in terms of pressure or volume based on the reactants and products of the system, and so the position of equilibrium is unaffected by the addition of the inert gas. [SO 16. K eq 3 ][NO] [SO ][NO ] (3.00)(.00) (4.00)(0.500) 3.00 Add 1.5 NO to the 1.50 container. The [NO ] increases by 1.00 / [SO ] [NO ] [SO 3 ] [NO] I 4.00 1.50 3.00.00 C -x -x +x +x E 4.00 - x 1.50 - x 3.00 + x.00 + x K eq [SO 3][NO] [SO ][NO ] (3.00 + x)(.00 + x) 3.00 (4.00 - x)(1.500 - x) 6.00 + 5.00x + x 3.00 6.00-5.50x + x 3.00(6.00-5.50x + x ) (6.00 + 5.00x + x ) 18.00-16.50x + 3.00x 6.00 + 5.00x + x.00x - 1.50x + 1.00 0 x 1.50 ± 1.50-4(.00)(1.00) (.00) x 1.50 ± 19.1376 4 x 0.59 or x 10.159 The second value (x 10.159) is not possible because there would be more NO than the total of everything in the container. Therefore, x 0.59. [NO].00 + x.00 + 0.59.59 17. PCl 5 (g) PC 3 (g) + Cl (g) 18. I 0.90 1.50 [PCl 5 ] [Cl ] [PCl 3 ] 0.60 0.00 0.00 C -0.8 +0.8 +0.8 E 0.48 1.50 K eq [PCl 3][Cl ] [PCl 5 ] (0.8)(0.8) (0.3) 0.45 0.5 0.3 [Br ] [Cl ] [BrCl] I 4.00 4.00 0.00 C -x -x +x E 4.00 - x 4.00 - x x K eq [BrCl] [Br ][Cl ] (x) 47.5 (4.00 - x)(4.00 - x) (x) 47.5 (4.00 - x) 47.5 6.89 (x) (4.00 - x) (x) (4.00 - x) 6.89(4.00 - x) (x) 0.8 0.8 46 MHR

7.568-6.89x x 7.568 8.89x 7.568 x 8.89 x 3.10 [Br ] 4.00 - x 4.00-3.10 0.90 / [Cl ] 4.00 - x 4.00-3.10 0.90 / [BrCl] x (3.10) 6.0 / 18. [Br ] 0.90 /; [Cl ] 0.90 /; [BrCl] 6.0 / 19. Without balance, the equilibrium systems of the blood will not be able to occur as they would under ideal conditions. Most long term imbalances will lead to a wide variety of health related issues that can cause severe damage to many organs and organ systems. If left untreated, many can lead to damage that cannot be repaired. 0. Organizers must include the steps of: 1. Convert the acid dissociation constant to the base ionization constant using K w.. Write and balance the reaction of the ionization for the base. 3. Set up an ICE chart to find expressions for the equilibrium constants for all reactants and products. 4. Use the K b expression, with the value from step 1 and the equilibrium constants from step 3 to find the concentration of hydroxide ions in solution. 5. Find poh using the concentration found in step 4. 6. Use ph 14 - poh to find the ph. 1. ph log [H 3 O + ] log 0.00750.1 poh 14 - ph 14 -.1 11.88 [OH ][H 3 O + ] 10 14 [OH ] 10 14 [H 3 O + ] 10 14 0.00750 1.33333 10 1 1.33 10 1 ph.1; poh 11.88; [OH - ] 1.33 10-1 /. HCOOH(aq) + H O(l) H 3 O + (aq) + HCOO - [HCOOH] [H 3 O + ] [HCOO ] I 0.100 0.00 0.00 C -x +x +x E 0.100 - x x x K a 1.70 10 4 K a [H 3O + ][HCOO ] [HCOOH] 1.70 10 4 (x)(x) 0.100 - x 1.70 10 4 (0.100 - x) x 1.70 10 5-1.70 10 4 x x x + 1.70 10 4 x - 1.70 10 5 0 x 1.70 10 4 ± (1.70 10 4 ) - 4(1) (1.70 10 5 ) (1) x 1.70 10 4 ± 8.48 10 3 Use the positive value. x 4.039 10 3 ph log (4.039 10 3 ).3937.39 3. B(aq) + H O(l) BH + (aq) + HO (aq) Concentration of base: c n V m M V 3.75 g g 101.70 1.00 0.03687 1 0.03687 MHR 47

ph log [H 3 O + ] 9.14 log [H 3 O + ] [H 3 O + ] 10 9.14 [H 3 O + ] 7.44 10 10 / [H 3 O + ][OH ] 10 14 [OH 10 ] 14 [H 3 O + ] [OH 10 ] 14 7.44 10 10 [OH ] 1.3804 10 5 [B] [BH + ] [OH ] I 0.03687 0.00 0.00 C -1.3804 10 5 +1.3804 10 5 +1.3804 10 5 E 0.03687-1.3804 10 5 0.03856 K b [BH+ ][OH ] [B] (1.3804 10 5 )(1.3804 10 5 ) 0.036856 K b 5.17 10 9 1.3804 10 5 1.3804 10 5 4. Moles of NaOH: n cv 0.0180.547 10 4 (14.15 m) n HCl n NaOH.547 10 4 Initial concentration of HCl: c n V.547 10 4 5.00 m 1 1000 m 1000 m 1 1.0188 10 HCl is a strong acid so it dissociates completely. Therefore the concentration of hydronium ion is the same as the concentration of HCl. ph log [H 3 O + ] log (1.0188 10 ) 1.99 5. Water acts as a Brønsted-owry base in reactions with acids, such as hydrochloric acid, because it is a proton acceptor. Water functions as a Brønsted-owry acid, or a proton donor, in reactions with bases, such as ammonia. 48 MHR