Chapter 3. Thermochemistry: Energy Flow and Chemical Change. 5.1 Forms of Energy and Their Interconversion

Transcription

1 Chapter 3 Thermochemistry: Energy Flow and Chemical Change 5.1 Forms of Energy and Their Interconversion 5.2 Enthalpy: Chemical Change at Constant Pressure 5.3 Calorimetry: Measuring the Heat of a Chemical or Physical Change 5.4 Stoichiometry of Thermochemical Equations 5.5 Hess s Law: Finding ΔH of Any Reaction 5.6 Standard Enthalpies of Reaction (Δ r H ) 5-1

2 5.1 Forms of Energy and Their Interconversion Thermodynamics is the study of energy and its transformations. Thermochemistry is a branch of thermodynamics that deals with the heat involved in chemical and physical changes. When energy is transferred from one object to another, it appears as work and heat. 5-2

3 Figure 5.1 The System and Its Surroundings A chemical system and its surroundings. The system in this case is the contents of the reaction flask. The surroundings comprise everything else, including the flask itself. 5-3

4 System : Part of the Universe we are focusing on. Surroundings: Everything else outside of the system System + Surroundings = Universe The internal energy, U, of a system is the sum of the potential and kinetic energies of all the particles present. The total energy of the universe remains constant. A change in the energy of the system must be accompanied by an equal and opposite change in the energy of the surroundings. The total change in a system s internal energy is the sum of the energy transferred as heat(q) and work(w) U = q + w 5-4

5 Figure 5.2 Energy diagrams for the transfer of internal energy (E) between a system and its surroundings. Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display. ΔE = E final - E initial = E products - E reactants 5-5

6 Figure 5.3 The two cases where energy is transferred as heat only. Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 5-6

7 Figure 5.4A The two cases where energy is transferred as work only. The system does work on the surroundings. 5-7

8 Figure 5.4B The two cases where energy is transferred as work only. The system has work done on it by the surroundings. 5-8

9 Table 5.1 The Sign Conventions* for q, w, and ΔU q + w = ΔU depends on sizes of q and w depends on sizes of q and w - * For q: + means system gains heat; - means system releases heat. * For w: + means work done on system; - means work done by system. 5-9

10 The Law of Energy Conservation The first law of Thermodynamics states that the total energy of the universe is constant. Energy is conserved, and is neither created nor destroyed. Energy is transferred in the form of heat and/or work. Δ universe U = Δ system U + Δ surroundings U =

11 Units of Energy The SI unit of energy is the joule (J). 1 J = 1 kg m 2 /s 2 The calorie(cal) was once defined as the quantity of energy needed to raise the temperature of 1 g of water by 1 C. 1 cal = J 5-11

12 Sample Problem 5.1 Determining the Change in Internal Energy of a System PROBLEM: When gasoline burns in a car engine, the heat released causes the products CO 2 and H 2 O to expand, which pushes the pistons outward. Excess heat is removed by the car s radiator. If the expanding gases do 451 J of work on the pistons and the system releases 325 J to the surroundings as heat, calculate the change in energy (ΔU) in J/mol, kj/mol, and kcal/mol. PLAN: Define the system and surroundings and assign signs to q and w correctly. Then ΔU = q + w. The answer can then be converted from J to kj and to kcal. 5-12

13 Sample Problem 5.1 SOLUTION: Heat is given out by a chemical reaction, so it makes sense to define the system as the reactants and products involved. The pistons, the radiator and the rest of the car then comprise the surroundings. Heat is given out by the system, so q = J The gases expand to push the pistons, so the system does work on the surroundings and w = J 5-13 ΔU = q + w = 1 kj -776 J/mol x 103 J/mol = kj -325 J/mol + (-451 J/mol)= -776 J/mol 1 kcal kj/mol x kj/mol = kcal

14 5.2 Enthalpy: Chemical Change at Constant Pressure ΔU = q + w To determine ΔU, both heat and work must be measured. The most common chemical work is PV work the work done when the volume of a system changes in the presence of an external pressure. Enthalpy (H) is defined as U + PV so ΔH = ΔU + ΔPV If a system remains at constant pressure and its volume does not change much, then ΔH ΔU 5-14

15 Figure 5.6 Two different paths for the energy change of a system. Even though q and w for the two paths are different, the total ΔU is the same for both. 5-15

16 Figure 5.7 Pressure-volume work. An expanding gas pushing back the atmosphere does pv work (w = -PΔV). 5-16

17 ΔU as a measure of ΔH ΔH is the change in heat for a system at constant pressure. q P = ΔU+ PΔV = ΔH ΔH ΔU for reactions that do not involve gases for reactions in which the total amount (mol) of gas does not change for reactions in which q P is much larger than PΔV, even if the total mol of gas does change. 5-17

18 Figure 5.8 Enthalpy diagrams for exothermic and endothermic processes. Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display. CH 4 (g) + 2O 2 (g) CO 2 (g) + H 2 O(g) H 2 O(s) H 2 O(l) A Exothermic process Heat is given out. B Endothermic process Heat is taken in. 5-18

19 Sample Problem 5.2 Drawing Enthalpy Diagrams and Determining the Sign of ΔH PROBLEM: For each of the following cases, determine the sign of ΔH, state whether the reaction is exothermic or endothermic, and draw and enthalpy diagram. (a) H 2 (g) + ½O 2 (g) H 2 O(l) kj (b) 40.7 kj + H 2 O(l) H 2 O(g) PLAN: From each equation, note whether heat is a reactant or a product. If heat is taken in as a reactant, the process is endothermic. If heat is released as a product, the process is exothermic. For the enthalpy diagram, the arrow always points from reactants to products. For endothermic reactions, the products are at a higher energy than the reactants, since the reactants take in heat to form the products. 5-19

20 Sample Problem 5.2 SOLUTION: (a) H 2 (g) + ½O 2 (g) H 2 O(l) kj Heat is a product for this reaction and is therefore given out, so the reaction is exothermic. The reactants are at a higher energy than the products. H 2 (g) + ½ O 2 (g) (reactants) Energy H 2 O(l) ΔH = kj (products) EXOTHERMIC 5-20

21 Sample Problem 5.2 SOLUTION: (b) 40.7 kj + H 2 O(l) H 2 O(g) Heat is a reactant in this reaction and is therefore absorbed, so the reaction is endothermic. The reactants are at a lower energy than the products. H 2 O(g) (product) Energy H 2 O(l) ΔH = kj (reactant) ENDOTHERMIC 5-21

22 5.3 Calorimetry The specific heat capacity (c) of a substance is the quantity of heat required to change the temperature of 1 gram of the substance by 1 K. q = c x m x ΔT q = heat lost or gained c = specific heat capacity m = mass in g ΔT = T final - T initial The heat capacity is the heat required to change the temperature of The substance by 1K q = heat capacity x ΔT

23 Table 5.2 Specific Heat Capacities (c) of Some Elements, Compounds, and Materials * Substance Specific Heat Capacity (J/g K)* Substance Specific Heat Capacity (J/g K)* Elements Solid materials aluminum, Al wood 1.76 graphite,c cement 0.88 iron, Fe glass 0.84 copper, Cu granite 0.79 gold, Au steel 0.45 Compounds 5-23 * at 298 K(25 C) water, H 2 O(l) ethyl alcohol, C 2 H 5 OH(l) 2.46 ethylene glycol, (CH 2 OH) 2 (l) 2.42 carbon tetrachloride, CCl 4 (l) 0.862

24 Sample Problem 5.3 Finding the Quantity of Heat from a Temperature Change PROBLEM: A layer of copper welded to the bottom of a skillet weighs 125 g. How much heat is needed to raise the temperature of the copper layer from 25 C to 300. C? The specific heat capacity (c) of Cu is J/g K. PLAN: We know the mass (125 g) and c (0.387 J/g K) of Cu and can find ΔT in C, which equals ΔT in K. We can use the equation q = cmδt to calculate the heat. SOLUTION: ΔT = T final T initial = = 275 C = 275 K q = cmδt = J g K x 125 g x 275 K = 1.33x10 4 J 5-24

25 Figure 5.9 Coffee-cup calorimeter This device measures the heat transferred at constant pressure (q P ).

26 Sample Problem 5.4 Determining the Specific Heat Capacity of a Solid PROBLEM: You heat g solid in a test-tube to C and then add the solid to g of water in a coffee-cup calorimeter. The water temperature changes from C to C. Find the specific heat capacity of the solid. PLAN: Since the water and the solid are in contact, heat is transferred from the solid to the water until they reach the same T final. In addition, the heat given out by the solid (- q solid ) is equal to the heat absorbed by the water (q water ). SOLUTION: ΔT water = T final T initial = (28.49 C C) = 3.39 C = 3.39 K ΔT solid = T final T initial = (28.49 C C) = C = K 5-26

27 Sample Problem 5.4 c solid = c x mass x ΔT H 2 O H 2 O H 2 O mass solid x ΔT solid J/g K x g x 3.39 K = = J/g K g x ( K) 5-27

28 Sample Problem 5.5 Determining the Enthalpy Change of an Aqueous Reaction PROBLEM: You place 50.0 ml of M NaOH in a coffee-cup calorimeter at o C and add 25.0 ml of M HCl, also at o C. After stirring, the final temperature is o C. (Assume that the total volume is the sum of the individual volumes, also assume that the final solution has the same density (1.00 g/ml) and specific heat capacity (table 5.2) as water. (a) Calculate q soln (J) (b) Calculate the change in enthalpy, ΔH, of the reaction (kj/mol of H 2 O formed). PLAN: Heat flows from the reaction (the system) to its surroundings (the solution). Since q rxn = q soln, we can find the heat of the reaction by calculating the heat absorbed by the solution. 5-28

29 Sample Problem 5.5 SOLUTION: (a) To find q soln : Total mass (g) of the solution = (25.0 ml ml) x 1.00 g/ml = 75.0 g ΔT soln = C C = 2.21 C = 2.21 K q soln = c soln x mass soln x ΔT soln = (4.184 J/g K)(75.0 g)(2.21 K) = 693 J (b) To find ΔH rxn we first need a balanced equation: HCl(aq) + NaOH(aq) NaCl(aq) + H 2 O(l) 5-29

30 Sample Problem 5.5 For HCl: 25.0 ml HCl x 1 L 10 3 ml x mol 1 L x 1 mol H 2 O 1 mol HCl = mol H 2 O For NaOH: 50.0 ml NaOH x 1 L 10 3 ml x mol 1 L x 1 mol H 2 O 1 mol NaOH = mol H 2 O HCl is limiting, and the amount of H 2 O formed is mol. ΔH rxn = q rxn mol H 2 O = -693 J x mol 1 kj 10 3 J = kj/mol H 2 O 5-30

31 Figure 5.10 A bomb calorimeter This device measures the heat released at constant volume (q V ).

32 Sample Problem 5.6 Calculating the Heat of a Combustion Reaction PROBLEM: A manufacturer claims that its new dietetic dessert has fewer than 10 Calories per serving. To test the claim, a chemist at the Department of Consumer Affairs places one serving in a bomb calorimeter and burns it in O 2. The initial temperature is C and the temperature rises to C. If the heat capacity of the calorimeter is kj/k, is the manufacturer s claim correct? PLAN: When the dessert (system) burns, the heat released is absorbed by the calorimeter: -q system = q calorimeter To verify the energy provided by the dessert, we calculate q calorimeter. 5-32

33 Sample Problem 5.6 SOLUTION: ΔT calorimeter = T final T initial = C C = C = K q calorimeter = heat capacity x ΔT = kj/k x K = kj kj x kcal kj = 9.63 kcal or Cal The manufacturer s claim is true, since the heat produced is less than 10 Calories. 5-33

34 5.4 Stoichiometry of Thermochemical Equations A thermochemical equation is a balanced equation that includes Δ r H. example: 2H 2 O(l) 2H 2 (g) + O 2 (g) ΔH = 572 kj The sign of ΔH indicates whether the reaction is exothermic or endothermic. The magnitude of ΔH is proportional to the amount of substance. The value of ΔH can be used in a calculation in the same way as a mole ratio. 5-34

35 Figure 5.11 The relationship between amount (mol) of substance and the energy (kj) transferred as heat during a reaction 5-35

36 Sample Problem 5.7 Using the Enthalpy Change of a Reaction (ΔH) to Find Amounts of Substance PROBLEM: The major source of aluminum in the world is bauxite (mostly aluminum oxide). Its thermal decomposition can be represented by the equation: Al 2 O 3 (s) 2Al(s) O 2 (g) ΔH = 1676 kj If aluminum is produced this way, how many grams of aluminum can form when 1.000x10 3 kj of heat is transferred? PLAN: From the balanced equation and ΔH, we see that 2 mol of Al is formed when 1676 kj of heat is absorbed. heat (kj) 1676 kj = 2 mol Al mol of Al mass (g) of Al multiply by M (g/mol) 5-36

37 Sample Problem 5.7 SOLUTION: 1.000x10 3 kj x 2 mol Al 1676 kj x g Al 1 mol Al = g Al 5-37

38 5.5 Hess Law Hess s law states that the enthalpy change of an overall process is the sum of the enthalpy changes of its individual steps. Δ overall H = Δ 1 H + Δ 2 H +. + Δ n H ΔH for an overall reaction can be calculated if the ΔH values for the individual steps are known. 5-38

39 Calculating ΔH for an overall process Identify the target equation, the step whose ΔH is unknown. Note the amount of each reactant and product. Manipulate each equation with known ΔH values so that the target amount of each substance is on the correct side of the equation. Change the sign of ΔH when you reverse an equation. Multiply amount (mol) and ΔH by the same factor. Add the manipulated equations and their resulting ΔH values to get the target equation and its ΔH. All substances except those in the target equation must cancel. 5-39

40 Sample Problem 5.8 Using Hess s Law to Calculate an Unknown ΔH PROBLEM: Two pollutants that form in auto exhausts are CO and NO. An environmental chemist must convert these pollutants to less harmful gases through the following reaction: CO(g) + NO(g) CO 2 (g) + ½N 2 (g) ΔH =? Given the following information, calculate the unknown ΔH: Equation A: CO(g) + ½ O 2 (g) CO 2 (g) Δ A H = kj/mol Equation B: N 2 (g) + O 2 (g) 2NO(g) Δ B H = kj/mol PLAN: Manipulate Equations A and/or B and their ΔH values to get to the target equation and its ΔH. All substances except those in the target equation must cancel. 5-40

41 Sample Problem 5.8 SOLUTION: Multiply Equation B by ½ and reverse it, ΔH sign changed NO(g) ½ N 2 (g) + ½ O 2 (g); ΔH = kj Add the manipulated equations together: Equation A: CO(g) + ½ O 2 (g) CO 2 (g) Δ A H = kj/mol -½ Equation B: NO(g) ½ N 2 (g) + ½ O 2 (g) Δ -1/2B H = kj/mol CO(g) + NO(g) CO 2 (g) + ½ N 2 (g) Δ C H = kj/mol 5-41

42 5.6 Standard Enthalpies of Reaction ( r H ) Standard Enthalpy of Reaction ( r H ) is the enthalpy change of the reaction measured in Standard State. For a gas, standard state is 1 bar and ideal behavior For aqueous solutions, standard state is 1M concentration For a pure substance, standard state is the most stable form at 1 bar and the temperature of interest ( usually 25 C Standard Enthalpy of Formation ( f H ) is the enthalpy change associated with the formation of 1 mol of a compound from its elements, in standard state r H = Σ m f H (products) Σ n f H (reactats) 5-42

43 Table 5.3 Selected Standard Enthalpies of Formation at 25 C (298.15K) 5-43 Formula Calcium Ca(s) CaO(s) CaCO 3 (s) Carbon C(graphite) C(diamond) CO(g) CO 2 (g) CH 4 (g) CH 3 OH(l) HCN(g) CS s (l) Chlorine Cl(g) Δ f H (kj/mol) Formula Cl 2 (g) HCl(g) Hydrogen H(g) H 2 (g) Nitrogen N 2 (g) NH 3 (g) NO(g) Oxygen O 2 (g) O 3 (g) H 2 O(g) H 2 O(l) Δ f H (kj/mol) Formula Δ f H (kj/mol) Silver Ag(s) AgCl(s) Sodium Na(s) Na(g) NaCl(s) Sulfur S 8 (rhombic) 0 S 8 (monoclinic) 0.3 SO 2 (g) SO 3 (g)

44 Sample Problem 5.9 Writing Formation Equations PROBLEM: Write a balanced formation equation for each of the following compounds including the value of Δ f H. (a) AgCl (s) (b) CaCO 3(s) (c) HCN (g). PLAN: Write the elements as reactants and 1 mol of the compound as the product formed. Make sure all substances are in their standard states. Balance the equations and find the value of Δ f H in Table 5.3 or Appendix B. 5-44

45 Sample Problem 5.9 SOLUTION: (a) Silver chloride, AgCl, a solid at standard conditions. Ag(s) + ½Cl 2 (g) AgCl(s) Δ f H = kj/mol (b) Calcium carbonate, CaCO 3, a solid at standard conditions. 3 Ca(s) + C(graphite) + 2 O 2 (g) CaCO 3 (s) Δ f H = kj/mol (c) Hydrogen cyanide, HCN, a gas at standard conditions. ½H 2 (g) + C(graphite) + ½N 2 (g) HCN(g) Δ f H = 135 kj/mol 5-45

46 Figure 5.12 The two-step process for determining Δ r H from Δ f H values. 5-46

47 Sample Problem 5.10 Calculating ΔH rxn from ΔH f Values PROBLEM: Nitric acid is used to make many products, including fertilizer, dyes, and explosives. The first step in the industrial production process is the oxidation of ammonia: 4NH 3 (g) + 5O 2 (g) 4NO(g) + 6H 2 O(g) Calculate Δ r H from Δ f H values. PLAN: Use the Δ f H values from Table 5.3 or Appendix B and apply the equation ΔH rxn = Σ mδ f H (products) - Σ nδ fh (reactants) 5-47

48 Sample Problem 5.10 SOLUTION: Δ r H = Σ mδ f H (products) - Σ nδ f H (reactants) Δ r H = [4(Δ f H o of NO(g) + 6(Δ f H o of H 2 O(g)] - [4(ΔH of NH 3 (g) + 5(ΔH of O 2 (g)] = (4 mol)(90.3 kj/mol) + (6 mol)( kj/mol) [(4 mol)(-45.9 kj/mol) + (5 mol)(0 kj/mol)] = -906 kj/mol Δ r H = -906 kj/mol 5-48

49 Figure 8.8 The Born-Haber cycle for lithium fluoride. 5-49

50 A simple Born-Haber cycle can be represented as follows; Unbound gaseous ions Breaking bonds Forming gases Forming cations,anions Lattice energy Metal and nonmetal Ionic compound 5-50

51 Table 8.2 Average Bond Energies (kj/mol) and Bond Lengths (pm) 5-51

52 Table 8.3 The Relation of Bond Order, Bond Length, and Bond Energy 5-52

53 8.4 Bond Energies and Δ r H o The heat released or absorbed during a chemical change is due to differences between the bond energies of reactants and products. Δ r H = ΣΔ reactant bonds broken H + ΣΔ product bonds formed H 5-53

54 Figure 8.19 Using bond energies to calculate ΔH rxn for HF formation. 5-54

55 Figure 8.20 Using bond energies to calculate ΔH rxn for the combustion of methane. 5-55

56 Sample Problem 8.4 Using Bond Energies to Calculate ΔH rxn PROBLEM: Calculate ΔH rxn for the chlorination of methane to form trichloromethane( chloroform). bonds broken ΣΔH positive bonds formed ΣΔH negative PLAN: All the reactant bonds break, and all the product bonds form. Find the bond energies in Table 9.2 and substitute the two sums, with correct signs, into Equation

57 Sample Problem 8.4 SOLUTION: For bonds broken: 4 x C-H = (4 mol)(413 kj/mol) = 1652 kj 3 x Cl-Cl = (3 mol)(243 kj/mol) = 729 kj ΣΔ bonds broken H = 2381 kj For bonds formed: 3 x C-Cl = (3 mol)(-339 kj/mol) = kj 1 x C-H = (1 mol)(-413 kj/mol) = -413 kj 3 x H-Cl = (3 mol)(-427 kj/mol) = kj ΣΔ bonds formed H = kj Δ reaction H = ΣΔ bonds broken H + ΣΔ bonds formed H = 2381 kj + (-2711 kj) = kj 5-57

58 Figure 8.21 Relative bond strength and energy from fuels. 5-58