front 1 1. A system that does no work but which transfers heat to the surroundings has A) q < 0, DE > 0. D) q > 0, DE < 0. B) q < 0, DE < 0. E) q < 0, DE = 0. C) q > 0, DE > 0. | back 1 b |
front 2 2. A system that does no work but which receives heat from the surroundings has A) q < 0, DE > 0. D) q = –DE. B) q > 0, DE < 0. E) w = DE. C) q = DE. | back 2 c |
front 3 A system which undergoes an adiabatic change (i.e., q = 0) and does work on the surroundings has 3. A system which undergoes an adiabatic change (i.e., q = 0) and does work on the surroundings has A) w < 0, DE = 0. D) w < 0, DE > 0. B) w > 0, DE > 0. E) w < 0, DE < 0. C) w > 0, DE < 0. | back 3 e |
front 4 4. A system which undergoes an adiabatic change (i.e., q = 0) and has work done on it by the surroundings has A) w = DE. D) w < 0, DE > 0. B) w = –DE. E) w > DE. C) w > 0, DE < 0. | back 4 a |
front 5 5. A system receives 575 J of heat and delivers 425 J of work. Calculate the change in the internal energy, DE, of the system. A) –150 J B) 150 J C) –1000 J D) 1000 J E) 575 J | back 5 b |
front 6 A system delivers 225 J of heat to the surroundings while delivering 645 J of work. Calculate the change in the internal energy, DE, of the system. A) –420 J B) 420 J C) –870 J D) 870 J E) –225 J | back 6 c |
front 7 7. A system delivers 1275 J of heat while the surroundings perform 855 J of work on it. Calculate DE in J. A) –2130 J B) –420 J C) 420 J D) 2130 J E) –1275 J | back 7 b |
front 8 8. A system absorbs 21.6 kJ of heat while performing 6.9 kJ of work on the surroundings. If the initial internal energy, E, is 61.2 kJ, what is the final value of E? A) 32.7 kJ B) 46.5 kJ C) 75.9 kJ D) 82.8 kJ E) 89.7 kJ | back 8 c |
front 9 9. A system initially has an internal energy E of 501 J. It undergoes a process during which it releases 111 J of heat energy to the surroundings, and does work of 222 J. What is the final energy of the system, in J? A) 168 J B) 390 J C) 612 J D) 834 J E) cannot be calculated without more information | back 9 a |
front 10 10. A system expands from a volume of 1.00 L to 2.00 L against a constant external pressure of 1.00 atm. The work (w) done by the system, in J, is A) 1.00 J. D) 1.01 × 105 J. B) 2.00J. E) none of the above. C) 1.01 × 102 J. | back 10 c |
front 11 11. A system contracts from an initial volume of 15.0 L to a final volume of 10.0 L under a constant external pressure of 0.800 atm. The value of w, in J, is A) –4.0 J. B) 4.0 J. C) –405 J. D) 405 J. E) 4.05 × 103 J. | back 11 d |
front 12 12. An ideal gas (the system) is contained in a flexible balloon at a pressure of 1 atm and is initially at a temperature of 20.°C. The surrounding air is at the same pressure, but its temperature is 25°C. When the system has equilibrated with its surroundings, both systems and surroundings are at 25°C and 1 atm. In changing from the initial to the final state, which one of the following relationships regarding the system is correct? A) DE < 0 B) DE = 0 C) DH = 0 D) w > 0 E) q > 0 | back 12 e |
front 13 13. Which one of the following relationships is always correct? A) potential energy + kinetic energy = constant B) E = q + w C) DE = DH – PDV D) H = E + PV E) DH = q v | back 13 d |
front 14 14. In which of the following processes is DH = DE ? A) Two moles of ammonia gas are cooled from 325°C to 300°C at 1.2 atm. B) One gram of water is vaporized at 100°C and 1 atm. C) Two moles of hydrogen iodide gas react to form hydrogen gas and iodine gas in a 40-L container. D) Calcium carbonate is heated to form calcium oxide and carbon dioxide in a container with variable volume. E) One mole of solid carbon dioxide sublimes to the gas phase. | back 14 c |
front 15 15. For which one of the following reactions will DH be approximately (or exactly) equal to DE? A) H2(g) + Br2(g) ® 2HBr(g) B) H2O(l) ® H2O(g) C) CaCO3(s) ® CaO(s) + CO2(g) D) 2H(g) + O(g) ® H2O(l) E) CH4(g) + 2O2(g) ® CO2(g) + 2H2O(l) | back 15 a |
front 16 16. In which one of the following reactions would you expect DH to be substantially greater than DE (i.e., DH > DE)? A) H2(g) + Br2(g) ® 2HBr(g) B) CO2(s) ® CO2(g) C) C2H2(g) + H2(g) ® C2H4(g) D) H2O(s) ® H2O(l) E) HCl(aq) + NaOH(aq) ® NaCl(aq) + H2O(l) | back 16 b |
front 17 17. Cold packs, whose temperatures are lowered when ammonium nitrate dissolves in water, are carried by athletic trainers when transporting ice is not possible. Which of the following is true of this reaction? A) DH < 0, process is exothermic D) DH > 0, process is endothermic B) DH > 0, process is exothermic E) DH = 0, since cold packs are sealed C) DH < 0, process is endothermic | back 17 d |
front 18 18. In a phase change of water between the liquid and the gas phases, 770.1 kJ of energy was released by the system. What was the product, and how much of it was formed in the phase change? (Data: H2O(l) ® H2O(g) DH = 44.01 kJ/mol.) A) 315 g water vapor was produced. B) 17.5 g of water vapor was produced. C) 17.5 mol of water vapor was produced. D) 17.5 mol of liquid water was produced. E) 17.5 g of liquid water was produced. | back 18 d |
front 19 19. The dissolution of barium hydroxide in water is an exothermic process. Which of the following statements is correct? A) The enthalpy of solid barium hydroxide plus pure water is less than that of the solution, at the same temperature. B) The enthalpy of solid barium hydroxide plus pure water is greater than that of the solution, at the same temperature. C) The enthalpy of solid barium hydroxide plus pure water is the same as that of the solution, at the same temperature. D) The temperature of the solution is lower than of the barium hydroxide and water before mixing. E) When barium hydroxide dissolves in water, the system does work on the surroundings. | back 19 b |
front 20 20. Two solutions (the system), each of 25.0 mL volume and at 25.0°C, are mixed in a beaker. A reaction occurs between them, and the temperature rises to 35.0°C. After the products have equilibrated with the surroundings, the temperature is again 25.0°C and the total volume is 50.0 mL. No gases are involved in the reaction. Which one of the following relationships concerning the change from initial to final states (both at 25.0°C) is correct? A) DE = 0 B) DH = 0 C) DE > 0 D) q = 0 E) w = 0 | back 20 e |
front 21 21. A Snickers® candy bar contains 280 Calories, of which the fat content accounts for 120 Calories. What is the energy of the fat content, in kJ? A) 5.0 × 10–1 kJ D) 1.2 × 103 kJ B) 29 kJ E) 5.0 × 105 kJ C) 5.0 × 102 kJ | back 21 c |
front 22 22. Your favorite candy bar, Gummy Beakers, contains 1.2 × 106 J of energy while your favorite soft drink, Bolt, contains 6.7 × 105 J. If you eat two packs of Gummy Beakers a day and drink 3 cans of Bolt, what percent of your 2000 Calorie daily food intake is left for broccoli, beans, beef, etc.? A) 53% B) 47% C) 27% D) 11% E) 0% | back 22 b |
front 23 23. Natural gas, or methane, is an important fuel. Combustion of one mole of methane releases 802.3 kilojoules of energy. How much energy does that represent in kilocalories? A) 1.92 × 10–1 kcal D) 1.92 × 105 kcal B) 1.92 × 102 kcal E) 3.36 × 106 kcal C) 3.36 × 103 kcal | back 23 b |
front 24 24. Which of the following is not a state function? A) internal energy B) volume C) work D) pressure E) enthalpy | back 24 c |
front 25 25. Calculate q when 28.6 g of water is heated from 22.0°C to 78.3°C. A) 0.385 kJ B) 1.61 kJ C) 6.74 kJ D) 9.37 kJ E) 1.61 × 103 kJ | back 25 c |
front 26 If, as a pioneer, you wished to warm your room by taking an object heated on top of a pot-bellied stove to it, which of the following 15-pound objects, each heated to 100°C, would be the best choice? The specific heat capacity (in J/(g·K)) for each substance is given in parentheses. Iron (0.450), copper (0.387), granite (0.79), gold (0.129), water (4.18). A) iron B) copper C) granite D) gold E) water | back 26 e |
front 27 27. Ethylene glycol, used as a coolant in automotive engines, has a specific heat capacity of 2.42 J/(g·K). Calculate q when 3.65 kg of ethylene glycol is cooled from 132°C to 85°C. A) –1900 kJ B) –420 kJ C) –99 kJ D) –0.42 kJ E) –4.2 × 10–6 kJ | back 27 b |
front 28 28. A 275-g sample of nickel at 100.0°C is placed in 100.0 mL of water at 22.0°C. What is the final temperature of the water? Assume that no heat is lost to or gained from the surroundings. Specific heat capacity of nickel = 0.444 J/(g·K) A) 39.6°C B) 40.8°C C) 61.0°C D) 79.2°C E) 82.4°C | back 28 a |
front 29 29. Benzene is a starting material in the synthesis of nylon fibers and polystyrene (styrofoam). Its specific heat capacity is 1.74 J/(g·K). If 16.7 kJ of energy is absorbed by a 225-g sample of benzene at 20.0°C, what is its final temperature? A) –22.7°C B) 36.7°C C) 42.7°C D) 62.7°C E) none of the above | back 29 d |
front 30 30. When Karl Kaveman adds chilled grog to his new granite mug, he removes 10.9 kJ of energy from the mug. If it has a mass of 625 g and was at 25°C, what is its new temperature? Specific heat capacity of granite = 0.79 J/(g·K) A) 3°C B) 14°C C) 22°C D) 47°C E) none of the above | back 30 a |
front 31 31. The Starship Enterprise is caught in a time warp and Spock is forced to use the primitive techniques of the 20th century to determine the specific heat capacity of an unknown mineral. The 307-g sample was heated to 98.7°C and placed into a calorimeter containing 72.4 g of water at 23.6°C. The heat capacity of the calorimeter was 15.7 J/K. The final temperature in the calorimeter was 32.4°C. What is the specific heat capacity of the mineral? A) 0.124 J/(g·K) D) 0.145 J/(g·K) B) 0.131 J/(g·K) E) none of the above C) 0.138 J/(g·K) | back 31 c |
front 32 A piece of copper metal is initially at 100.0°C. It is dropped into a coffee cup calorimeter containing 50.0 g of water at a temperature of 20.0°C. After stirring, the final temperature of both copper and water is 25.0°C. Assuming no heat losses, and that the specific heat (capacity) of water is 4.18 J/(g·K), what is the heat capacity of the copper in J/K? A) 2.79 J/K B) 3.33 J/K C) 13.9 J/K D) 209 J/K E) none of the above | back 32 c |
front 33 33. 15.0 g of ice cubes at 0.0°C are combined with 150. g of liquid water at 70.0°C in a coffee cup calorimeter. Calculate the final temperature reached, assuming no heat loss or gain from the surroundings. (Data: specific heat capacity of H2O(l), c = 4.18 J/g×°C; H2O(s) ® H2O(l) DH = 6.02 kJ/mol) A) 0.0 B) 10.6 C) 30.7 D) 43.2 E) 56.4 | back 33 e |
front 34 34. 40.0 g of ice cubes at 0.0°C are combined with 150. g of liquid water at 20.0°C in a coffee cup calorimeter. Calculate the final temperature reached, assuming no heat loss or gain from the surroundings. (Data: specific heat capacity of H2O(l), c = 4.18 J/g×°C; H2O(s) ® H2O(l) DH = 6.02 kJ/mol) A) 0.0 B) 10.6 C) 30.7 D) 43.2 E) 56.4 | back 34 a |
front 35 35. What is the final temperature when 20.0 g of water at 25°C is mixed with 30.0 g of water at 80°C? A) 35°C B) 42°C C) 53°C D) 58°C E) 70°C | back 35 d |
front 36 A backpacker collects snow at 0°C, and places it in a cooking pot on a camp stove. It takes 643 kJ of heat energy to melt the snow and bring the water to boiling. Assuming no heat loss, and neglecting the specific heat capacity of the pot, calculate the mass of snow that the backpacker collected. (Data: specific heat capacity of liquid water, c = 4.18 J/g×K; and: H2O(s) ® H2O(l) DH = DH fusion = 6.02 kJ/mol) A) 1.92 kg B) 1.90 kg C) 1.52 kg D) 855 g E) < 800 g | back 36 d |
front 37 37. The specific heat capacity c of a metal is approximately related to its molar mass as follows: c × = 3R, where R is the universal gas constant, 8.314 J/mol×K. Use this relationship to identify the metal which has a specific heat capacity of 0.900 J/g×K. A) Li B) Sn C) Ca D) Al E) U | back 37 d |
front 38 38. The combustion of glucose (C6H12O6) with oxygen gas produces carbon dioxide and water. This process releases 2803 kJ per mole of glucose. When 3.00 mol of oxygen react in this way with glucose, what is the energy release in kcal? (Hint: Write a balanced equation for the combustion process.) A) 223.5 kcal B) 335.3 kcal C) 1402 kcal D) 2012 kcal E) 5858 kcal | back 38 b |
front 39 39. A common laboratory reaction is the neutralization of an acid with a base. When 50.0 mL of 0.500 M HCl at 25.0°C is added to 50.0 mL of 0.500 M NaOH at 25.0°C in a coffee cup calorimeter, the temperature of the mixture rises to 28.2°C. What is the heat of reaction per mole of acid? Assume the mixture has a specific heat capacity of 4.18 J/(g·K) and that the densities of the reactant solutions are both 1.00 g/mL. A) 670 J B) 1300 J C) 27 kJ D) 54 kJ E) > 100 kJ | back 39 d |
front 40 40. Sand is converted to pure silicon in a three step process. The third step is SiCl4(g) + 2Mg(s) ® 2MgCl2(s) + Si(s) DH = –625.6 kJ What is the enthalpy change when 25.0 mol of silicon tetrachloride is converted to elemental silicon? A) –25.0 kJ D) –3.13 × 104 kJ B) –7820 kJ E) none of the above C) –1.56 × 104 kJ | back 40 c |
front 41 41. Calcium hydroxide, which reacts with carbon dioxide to form calcium carbonate, was used by the ancient Romans as mortar in stone structures. The reaction for this process is Ca(OH)2(s) + CO2(g) ® CaCO3(s) + H2O(g) DH = –69.1 kJ What is the enthalpy change if 3.8 mol of calcium carbonate is formed? A) –18 kJ B) –69 kJ C) –73 kJ D) –260 kJ E) none of the above | back 41 d |
front 42 42. Galena is the ore from which elemental lead is extracted. In the first step of the extraction process, galena is heated in air to form lead(II) oxide. 2PbS(s) + 3O2(g) ® 2PbO(s) + 2SO2(g) DH = –827.4 kJ What mass of galena is converted to lead oxide if 975 kJ of heat are liberated? A) 203 g B) 282 g C) 406 g D) 478 g E) 564 g | back 42 e |
front 43 43. The highly exothermic thermite reaction, in which aluminum reduces iron(III) oxide to elemental iron, has been used by railroad repair crews to weld rails together. 2Al(s) + Fe2O3(s) ® 2Fe(s) + Al2O3(s) DH = –850 kJ What mass of iron is formed when 725 kJ of heat are released? A) 47 g B) 65 g C) 95 g D) 112 g E) 130 g | back 43 c |
front 44 44. Use Hess's Law to calculate the enthalpy change for the reaction WO3(s) + 3H2(g) ® W(s) + 3H2O(g) from the following data: 2W(s) + 3O2(g) ® 2WO3(s) DH = –1685.4 kJ 2H2(g) + O2(g) ® 2H2O(g) DH = –477.84 kJ A) 125.9 kJ B) 252.9 kJ C) 364.9 kJ D) 1207.6 kJ E) none of the above | back 44 a |
front 45 45. Calculate the enthalpy change for the reaction NO(g) + O(g) ® NO2(g) from the following data: NO(g) + O3(g) ® NO2(g) + O2(g) DH = –198.9 kJ O3(g) ® 1.5O2(g) DH = –142.3 kJ O2(g) ® 2O(g) DH = 495.0 kJ A) –551.6 kJ B) –304.1 kJ C) 190.9 kJ D) 153.8 kJ E) 438.4 kJ | back 45 b |
front 46 46. Use the following data to calculate the standard heat (enthalpy) of formation, DH°f , of manganese(IV) oxide, MnO2 (s). 2MnO2(s) ® 2MnO(s) + O2(g) DH = 264 kJ MnO2(s) + Mn(s) ® 2MnO(s) DH = –240 kJ A) –504 kJ B) –372 kJ C) –24 kJ D) 24 kJ E) 504 kJ | back 46 a |
front 47 47. The compound carbon suboxide, C3O2, is a gas at room temperature. Use the data supplied to calculate the heat of formation of carbon suboxide. (Data: 2CO(g) + C(s) ® C3O2(g) DH° = 127.3 kJ/mol and: DH f ° of CO(g) = –110.5 kJ/mol) A) 116.8 B) –93.7 C) 227.8 D) –348.3 E) 93.7 | back 47 b |
front 48 48. Stoichiometric amounts of nitrogen gas and hydrogen gas react in a calorimeter to produce 5.00 g of ammonia gas. The calorimeter temperature rises 0.42°C. The calorimeter and water have a combined heat capacity of 32.16 kJ/K. Calculate the heat of formation of ammonia, DH f °, in kJ/mol. The formation reaction for ammonia is: 0.5N2(g) + 1.5H2(g) ® NH3(g). A) –46 kJ/mol D) 3.97 kJ/mol B) –13.5 kJ/mol E) 13.5 kJ/mol C) –3.97 kJ/mol | back 48 a |
front 49 49. Which one of the following statements about standard states is incorrect? A) The standard state of a solid compound is the pure solid. B) The standard state of a liquid compound is the pure liquid. C) The standard state of a gaseous compound is the gas at a pressure of 1 atmosphere. D) The standard state of an aqueous solute is a saturated solution in water. E) The standard state of an element is the form in which it is stable at 1 atm and a specified temperature, usually 25°C. | back 49 d |
front 50 50. Which one of the following equations represents the formation reaction of CH3OH(l)? A) C(g) + 2H2(g) + O2 (g) ® CH3OH(l) B) C(g) + 4H(g) + O(g) ® CH3OH(l) C) C(graphite) + 4H(g) + O(g) ® CH3OH(l) D) C(diamond) + 4H(g) + O(g) ® CH3OH(l) E) C(graphite) + 2H2(g) + O2(g) ® CH3OH(l) | back 50 e |
front 51 51. Which one of the following is not a correct formation reaction? (products are correct) A) H2(g) + O(g) ® H2O(l) B) H2(g) + Cl2(g) ® HCl(g) C) 6C(graphite) + 3H2(g) ® C6H6(l) D) C(graphite) ® C(diamond) E) 6C(graphite) + 6H2(g) + 3O2(g) ® C6H12O6(s) | back 51 a |
front 52 52. Which one of the following is a correct formation reaction? A) C(diamond) ® C(graphite) B) H2(g) + O(g) ® H2O(l) C) C(graphite) + 4H(g) ® CH4(g) D) 6C(graphite) + 6H2O(s) ® C6H12O6(s) E) 2C(graphite) + 3H2(g) + O2(g) ® C2H5OH(l) | back 52 e |
front 53 53. Calculate the DH°rxn for the decomposition of calcium carbonate to calcium oxide and carbon dioxide. DH°f [CaCO3(s)] = –1206.9 kJ/mol; DH°f [CaO(s)] = –635.1 kJ/mol; DH°f [CO2(g)] = –393.5 kJ/mol CaCO3(s) ® CaO(s) + CO2(g) A) –2235.5 kJ B) –1448.5 kJ C) –178.3 kJ D) 178.3 kJ E) 2235.5 kJ | back 53 d |
front 54 54. Nitric acid, which is among the top 15 chemicals produced in the United States, was first prepared over 1200 years ago by heating naturally occurring sodium nitrate (called saltpeter) with sulfuric acid and collecting the vapors produced. Calculate DH°rxn for this reaction. DH°f [NaNO3(s)] = –467.8 kJ/mol; DH°f [NaHSO4(s)] = –1125.5 kJ/mol; DH°f [H2SO4(l) = –814.0 kJ/mol; DH°f [HNO3(g)] = –135.1 kJ/mol NaNO3(s) + H2SO4(l) ® NaHSO4(s) + HNO3(g) A) –644.2 kJ B) –291.4 kJ C) –21.2 kJ D) 21.2 kJ E) 644.2 kJ | back 54 d |
front 55 55. An important step in the synthesis of nitric acid is the conversion of ammonia to nitric oxide. 4NH3(g) + 5O2(g) ® 4NO(g) + 6H2O(g) Calculate DH°rxn for this reaction. DH°f [NH3(g)] = –45.9 kJ/mol; DH°f [NO(g)] = 90.3 kJ/mol; DH°f [H2O(g)] = –241.8 kJ/mol A) –906.0 kJ B) –197.4 kJ C) –105.6 kJ D) 197.4 kJ E) 906.0 kJ | back 55 a |
front 56 56. Calculate the DH°rxn for the following reaction. (DH°f [SiO2(s)] = –910.9 kJ/mol; DH°f [SiCl4(g)] = –657.0 kJ/mol; DH°f [HCl(g)] = –92.3 kJ/mol; DH°f [H2O (g)] = –241.8 kJ/mol) SiO2(s) + 4HCl(g) ® SiCl4(g) + 2H2O(g) A) –139.5 kJ B) –137.4 kJ C) –104.4 kJ D) 104.4 kJ E) 139.5 kJ | back 56 e |
front 57 57. Calculate the DH°rxn for the following reaction. (DH°f [AsH3(g)] = 66.4 kJ/mol; DH°f [H3AsO4(aq)] = –904.6 kJ/mol; DH°f [H2O(l)] = –285.8 kJ/mol) H3AsO4(aq) + 4H2(g) ® AsH3(g) + 4H2O(l) A) –1981.4 kJ B) –685.2 kJ C) –172.2 kJ D) 172.2 kJ E) 685.2 kJ | back 57 c |
front 58 58. Ethanol, C2H5OH, is being promoted as a clean fuel and is used as an additive in many gasoline mixtures. Calculate the DH°rxn for the combustion of ethanol. (DH°f [C2H5OH(l)] = –277.7 kJ/mol; DH°f [CO2(g)] = –393.5 kJ/mol; DH°f [H2O(g)] = –241.8 kJ/mol) A) –1234.7 kJ B) –751.1 kJ C) –357.6 kJ D) 357.6 kJ E) 1234.7 kJ | back 58 a |