Exam #3 study guide (10-18-2022)

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Texas A&M University *

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Chemistry

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Feb 20, 2024

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Name: Student ID Number: TVN CHEM 1412 FALL 2022 EXAM #3 1. A 53.7 mL sample of a 0.706 M solution of NH 3 which is a weak base has a base ionization constant value of K b = 1.80 x 10 -5 at 25°C is being titrated by a 0.206 M solution of H 2 SO 4 which is a strong diprotic acid. Calculate the pH prior to the addition of any H 2 SO 4 . Let B = NH 3 , HB = NH 4 + , and let H 2 A = H 2 SO 4 B + H2O HB + OH - NH 3 + H 2 O NH 4 + + OH - Now create your I.C.E. table. NH 3 NH 4 + OH - Initial (M) 0.706 0.0 0.0 Change -x +x +x Equilibrium 0.706 – x x x K b = ¿¿ 1.80 x 10 5 = [ x ] x [ x ] [ 0.706 x ] 0.706 1.80 x 10 5 = 39,222 ( yes wecanapproximate ) 1.80 x 10 5 = [ x ] x [ x ] [ 0.706 ] 1.80 x 10 5 = x 2 [ 0.706 ]
Name: Student ID Number: x 2 = 1.2708 x 10 5 x = 3.5648 x 10 3 M NH 3 NH 4 + OH - Initial (M) 0.706 0.0 0.0 Change - 3.5648 x 10 3 M + 3.5648 x 10 3 M + 3.5648 x 10 3 M Equilibrium 0.7024352 M 3.5648 x 10 3 M 3.5648 x 10 3 M pOH =− log 10 ¿ pH = 14.00 2.45 = 11.55 2. A 53.7 mL sample of a 0.706 M solution of NH 3 which is a weak base has a base ionization constant value of K b = 1.80 x 10 -5 at 25°C is being titrated by a 0.206 M solution of H 2 SO 4 which is a strong diprotic acid. Calculate the pH when 5 mL of H 2 SO 4 has been added. 0.706 mole L x 0.0537 L 1 = 0.0379122 moles NH 3 0.206 mole L x 0.005 L 1 = 0.00103 moles H 2 SO 4 The stoichiometry is 2 moles of B (NH 3 ) for every 1 mole of H 2 SO 4 because if you write out the chemical equation as shown below.
Name: Student ID Number: H 2 SO 4 + 2NH 3 SO 4 2- + 2NH 4 + (aq) You can clearly see that 1 mole of H 2 SO 4 reacts with 2 moles of NH 3 (base) to produce 2 moles of NH 4 + (conjugate acid). 0.00103 moles H 2 SO 4 1 x 2 mole NH 3 1 mole H 2 SO 4 = 0.00206 molesof NH 3 equivalent ¿ 0.00103 moles H 2 SO 4 Your total solution volume is 53.7 + 5 = 58.7 mL = 0.0587 L. Now calculate your new molarity for NH 3 and NH 4 + . NH 3 adjusted moles = 0.0379122 0.00206 = 0.0358522 NH 4 + ¿ adjusted moles = 0.0 + 0.00206 = 0.00206 ¿ [ NH 3 ] = 0.0358522 moles 0.0587 L = 0.61077 M ¿ NH 3 + H 2 O NH 4 + + OH - By subtracting the equivalent moles of H 2 SO 4 from NH 3 and adding it to NH 4 + we have accounted for all the H 2 SO 4 added as titrant so now we can focus on NH 3 reaction with water (which is amphiprotic). Now create your I.C.E. table. NH 3 NH 4 + OH - Initial (M) 0.61077 0.035094 0.0 Change -x +x +x Equilibrium 0.61077 – x 0.035094 + x x K b = ¿¿ 1.80 x 10 5 = [ 0.035094 + x ] x [ x ] [ 0.61077 x ] 0.035094 1.80 x 10 5 = 1949.65 ( yes wecanapproximate ) 1.80 x 10 5 = [ 0.035094 ] x [ x ] [ 0.61077 ] x = ( 1.80 x 10 5 ) x ( 0.61077 ) 0.035094 = 3.1327 x 10 4 M
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Name: Student ID Number: NH 3 NH 4 + OH - Initial (M) 0.61077 0.035094 0.0 Change - 3.1327 x 10 4 + 3.1327 x 10 4 + 3.1327 x 10 4 Equilibrium 0.61045673 0.03540727 3.1327 x 10 4 pOH =− log 10 ¿ pH = 14.00 3.50 = 10.50 3. A 53.7 mL sample of a 0.706 M solution of NH 3 which is a weak base has a base ionization constant value of K b = 1.80 x 10 -5 at 25°C is being titrated by a 0.206 M solution of H 2 SO 4 which is a strong diprotic acid. Calculate the pH at the 2 nd equivalence point when all H 2 SO 4 has been converted into SO 4 2- . The stoichiometry is 2 moles of NH 3 for every 1 mole of H 2 SO 4 so we can use the initial moles of NH 3 and the stoichiometry to determine how many moles of H 2 SO 4 we need to reach the equivalence point and then we can use the molarity of H 2 SO 4 to determine the volume needed to reach the equivalence point. 0.0379122 moles B 1 x 1 mole H 2 SO 4 2 moles B = 0.0189561 molesof H 2 SO 4 ¿ reachequivalence point 0.0189561 moles of H 2 SO 4 1 x L 0.206 mole = 0.09202 L = 92.02 mL
Name: Student ID Number: Now that we are at the equivalence point the problem flips from a base equilibrium to an acid equilibrium type problem. NH 4 + + H 2 O K a NH 3 + H 3 O + 0.206 mole L x 0.09202 L 1 = 0.0189561 mole H 2 SO 4 NH 3 adjusted moles = 0.0379122 0.0379122 = 0.00 moles NH 4 + ¿ adjusted moles = 0.00 + 0.0379122 = 0.0379122 ¿ Your total solution volume is 53.7 + 92.02 = 145.72 mL = 0.14572 L. Now calculate your new molarity for HA and A - . [ NH 3 ] = 0.00 moles 0.14572 L = 0.00 M ¿ K a = 1 x 10 14 1.80 x 10 5 = 5.555 x 10 10 NH 4 + + H 2 O K a NH 3 + H 3 O + Now create an I.C.E.E. table. NH 4 + NH 3 H 3 O + Initial (M) 0.26017 0.0 0.0 Change -x +x +x Equilibrium 1 0.26017 – x x x Equilibrium 2 0.260158 1.20224 x 10 5 1.20224 x 10 5 K a = [ NH 3 ] x ¿¿ 5.555 x 10 10 = [ x ] x [ x ] [ 0.26017 x ] 5.555 x 10 10 = x 2 [ 0.26017 ] x = 1.20224 x 10 5 M pH =− log 10 ¿¿
Name: Student ID Number: 4. A 53.7 mL sample of a 0.706 M solution of NH 3 which is a weak base has a base ionization constant value of K b = 1.80 x 10 -5 at 25°C is being titrated by a 0.206 M solution of H 2 SO 4 which is a strong diprotic acid. Calculate the pH when 105.7 mL of H2SO4 has been added. excess volume = 105.7 92.02 = 13.68 mL = 0.01368 L 0.206 mole L x 0.01368 L 1 = 0.00281808 excess mole H 2 SO 4 Your total solution volume is 53.7 + 105.7 = 159.4 mL = 0.1594 L. [ H ¿ ¿ 2 SO 4 ] excess = 0.00281808 mole 0.1594 L = 0.017680 M ¿ The H 3 O + ion controls the pH and there is nothing left for H 2 SO 4 to react with except water which is amphiprotic. H 2 SO 4 (aq) + 2H 2 O (aq) SO 4 2- (aq) + 2H 3 O + (aq) Notice that for every 1 mole of H 2 SO 4 will react with 2 mole of H 2 O to form 2 moles of H 3 O + which is what dictates the pH. 0.00281808 mole H 2 SO 4 1 x 2 mole H 3 O + ¿ 1 mole H 2 SO 4 = 0.00563616 mole H 3 O + ¿¿ ¿ ¿ ¿ Whether you multiply the moles of H 2 SO 4 by 2 and then divide by the total solution volume or just multiply the molarity of H 2 SO 4 you get around 0.03536 M for H 3 O + . Now just simply take the negative logarithm base 10 of the [H 3 O + ] and you have the pH.
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Name: Student ID Number: pH =− log 10 ¿¿ 5. Suppose the K sp value for ? is ? so calculate the molar solubility in units of moles per liter or Molarity for the ? and the ? ions. 6. Suppose the Ksp value for ? is ?. Calculate the molar solubility in units of g/L for the ? and the ? ions. 7. Suppose the Ksp value for ? is ? so if a professor made ? mL of a ? solution then how many grams of the ? and the ? ions would be present in the solution. 8. Suppose the Ksp value for ? is ? and a professor made ? mL of this solution but then one of his graduate student accidentally poured in a few drops of a ? M solution of ? solution. Calculate the Qc value with this common ion effect and will a precipitate form or not? You may ignore the additional volume coming from the ? solution to simplify the calculation. 9. The K f value for ? (aq) is ?. What is the concentration of the ? ion (aq) and the ? ion aq) in a solution that is initially ? M of ? (aq) ?