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Chapter 7: Thermochemistry 273 20. (M) The amounts of the two reactants provided are the same as their stoichiometric coefficients in the balanced equation. Thus 852 kJ of heat is given off by the reaction. We can use this quantity of heat, along with the specific heat of the mixture, to determine the temperature change that will occur if all of the heat is retained in the reaction mixture. We make use of the fact that mass sp.ht. T . 5 2 3 2 3 2 3 102 g Al O 55.8 g Fe 0.8 J heat = 8.52 10 J = 1 mol Al O + 2 mol Fe 1 mol Al O 1 mol Fe g C T 5 3 1 1 8.52 10 J = = 5 10 C 214 g 0.8 J g C T The temperature needs to increase from 25 C to 1530 C or 3 = 1505 C = 1.5 10 CT . Since the actual T is more than three times as large as this value, the iron indeed will melt, even if a large fraction of the heat evolved is lost to the surroundings and is not retained in the products. 21. (M) (a) We first compute the heat produced by this reaction, then determine the value of H in kJ/mol KOH. 2calorimeter rxn J = 0.205 + 55.9 g 4.18 24.4 C 23.5 C = 2 10 J heat = g C q q H 2 10 0 205 5 10 2 1 J 1 kJ 1000J g 1mol KOH 56.1g KOH kJ / mol . (b) The here is known to just one significant figure (0.9 C). Doubling the amount of KOH should give a temperature change known to two significant figures (1.6 C) and using twenty times the mass of KOH should give a temperature change known to three significant figures (16.0 C). This would require 4.10 g KOH rather than the 0.205 g KOH actually used, and would increase the precision from one part in five to one part in 500, or 0.2 %. Note that as the mass of KOH is increased and the mass of H2O stays constant, the assumption of a constant specific heat becomes less valid. 22. (M) First we must determine the heat absorbed by the solute during the chemical reaction, qrxn. This is the negative of the heat lost by the solution, qsoln. Since the solution (water plus solute) actually gives up heat, the temperature of the solution drops. rxn 1 L 2.50 mol KI 20.3 kJ heat of reaction = 150.0 mL × × × = 7.61 kJ = 1000 mL 1 L soln 1 mol KI q rxn soln 1.30 g 2.7 J = = 150.0 mL 1 mL g C q q T 3 7.61 10 J 14 C 1.30g 2.7 J 150.0 mL 1mL g C T final = initial + = 23.5 C 14 C = 10. C T T T Chapter 7: Thermochemistry 274 23. (M) Let x be the mass, (in grams), of NH Cl4 added to the water. heat = mass sp.ht. T 4 44 1 mol NH Cl 14.7 kJ 1000 J × × × 53.49 g NH Cl 1 mol NH Cl 1 kJ x 1.00 g J = 1400 mL + 4.18 10. 25 C 1 mL g C x 4 4 2 4 8.8 10 275 = 8.8 10 + 63 ; = = 4.2 10 g NH Cl 275 63 x x x Our final value is approximate because of the assumed density (1.00 g/mL). The solution’s density probably is a bit larger than 1.00 g/mL. Many aqueous solutions are somewhat more dense than water. 24. (M) heat aOH H kJ= 500 mL 1 L 1000 mL 7.0 mol N 1 L soln 44.5 kJ 1 mol NaO = 1.6 102 = heat of r = heat abso =eaction rbed by solution OR rxn solnq q 51.6 10 J 74 C 1.08g 4.00J 500.mL 1mL g C T final 21 C +74 C = 95 CT 25. (E) We assume that the solution volumes are additive; that is, that 200.0 mL of solution is formed. Then we compute the heat needed to warm the solution and the cup, and finally H for the reaction. 31.02 g J Jheat = 200.0 mL 4.02 27.8 C 21.1 C + 10 27.8 C 21.1 C = 5.6 10 J 1 mL g C C 3 neutr 5.6 10 J 1 kJ = = 56 kJ/mol 55.6 kJ/mol to three significant figures 0.100 mol 1000 J H 26. (M) Neutralization reaction: 2NaOH aq + HCl aq NaCl aq + H O(l) Since NaOH and HCl react in a one-to-one molar ratio, and since there is twice the volume of NaOH solution as HCl solution, but the [HCl] is not twice the [NaOH], the HCl solution is the limiting reagent. 2 2 rxn soln 1 mol H O1 L 1.86 mol HCl 55.84 kJ heat released = 25.00 mL = 2.60 kJ 1000 mL 1 L 1 mol HCl 1 mol H O = heat of reaction = heat absorbed by solution or = q q 32.60 10 J 8.54 C 1.02g 3.98J 75.00mL 1mL g C T T = Tfinal Ti Tfinal = T + Ti 8.54 C + 24.72 C =33.26 CfinalT
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