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Consider a gas in a 1.0-L bulb at STP that is connected via a valve to another bulb that is initally evacuated. Answer the
following questions about what occurs when the valve between the two bulbs is opened.
Consider a process carried out on 1.00 mol of a monatomic ideal gas by the following two different pathways. The first
pathway is A (3.00 atm, 20.0 L) to C (1.00 atm, 20.0 L) to D (1.00 atm, 50.0 L); and the second pathway is A (3.00 atm, 20.0 L)
to B (3.00 atm, 50.0 L) to D (1.00 atm, 50.0 L). In each case, the gas is taken from state A to state D. 24. Calculate wAB.
A) -90 L•atm
B) 90 L•atm
C) -30 L•atm
D) 30 L•atm
E) 0
25. Calculate wAC.
A) -90 L•atm
B) 90 L•atm
C) -30 L•atm
D) 30 L•atm
E) 0
26. Calculate qAB.
A) 225 L•atm
B) -225 L•atm
C) 135 L•atm
D) -135 L•atm
E) none of these
27. Calculate qAC.
A) 60 L•atm
B) -60 L•atm
C) 100 L•atm
D) -100 L•atm
E) none of these
28. Which statement is true of a process in which 1 mol of a gas is expanded from state A to state B?
A) When the gas expands from state A to state B, the surroundings are doing work on the system.
B) The amount of work done in the process must be the same, regardless of the path.
C) It is not possible to have more than one path for a change of state.
D) The final volume of the gas will depend on the path taken.
E) The amount of heat released in the process will depend on the path taken.
29. For the vaporization of water at 1.00 atm,
H = 43.54 kJ/mol at 298 K and H = 40.68 kJ/mol at 373 K
The constant-pressure heat capacity of liquid water is 75.3 J/mol • K. Calculate the constant-pressure heat capacity for H2O(g).
A) 20.8 J/mol•K
B) 37.2 J/mol•K
C) 2790 J/mol•K
D) 75.3 J/mol•K
E) none of these
Two samples of a monatomic ideal gas are in separate containers at the same conditions of pressure, volume, and temperature
(V = 1.00 L and P = 1.00 atm). Both samples undergo changes in conditions and finish with V = 2.00 L and P = 2.00 atm.
However, in the first sample, the volume is changed to 2.0 L while the pressure is kept constant, and then the pressure is
increased to 2.00 atm while the volume remains constant. In the second sample, the opposite is done. The pressure is increased
first, with constant volume, and then the volume is increased under constant pressure.
30. Calculate the difference in E between the first sample and the second sample.
A) 0
B) 1.00 L•atm
C) 2.00 L•atm
D) 4.50 L•atm
E) none of these
31. Calculate the difference in w between the first sample and the second sample .
A) -2.00 L•atm
B) -1.00 L•atm
C) 1.00 L•atm
D) 2.00 L•atm
32. Calculate the difference in q between the first sample and the second sample.
A) -2.00 L•atm
B) -1.00 L•atm
C) 1.00 L•atm
D) 2.00 L•atm
E) none of these
Consider a process carried out on 1.00 mol of a monatomic ideal gas by the following two different pathways. The first
pathway is A (3.00 atm, 20.0 L) to C (1.00 atm, 20.0 L) to D (1.00 atm, 50.0 L); and the second pathway is A (3.00 atm, 20.0 L)
to B (3.00 atm, 50.0 L) to D (1.00 atm, 50.0 L). In each case, the gas is taken from state A to state D.
40. You take 326 g of a solid (melting point = 57.6°C, heat of fusion = 346 J/g) and let it melt in 757 g of water. The water
temperature decreases from its initial temperature to 57.6°C. Calculate the initial temperature of the water.
A) 93.2°C
B) 100.0°C
C) 22.0°C
D) 206.6°C
E) 249.8°C
41. A 140.0-g sample of water at 25.0°C is mixed with 100.0 g of a certain metal at 100.0°C. After thermal equilibrium is
established, the (final) temperature of the mixture is 29.6°C. What is the heat capacity of the metal, assuming it is constant over
the temperature range concerned?
A) 0.38 J/g°C
B) 0.76 J/g°C
C) 0.96 J/g°C
D) 0.031 J/g°C
E) none of these
42. A calorimeter contains 240 g of water at 21.6°C. A block of metal with a mass of 89 g is heated to 97.9°C and then placed in
the water in the calorimeter. After sufficient time, the temperature of the water is measured and found to be 27.0°C. Calculate
the specific heat capacity per gram of metal. Assume no heat is lost to the calorimeter or the surroundings.
A) 0.12 J/g°C
B) 0.86 J/g°C
C) 1.2 J/g°C
D) 0.21 J/g°C
E) 0.028 J/g°C
One mole of a liquid is vaporized at its boiling point, 65°C and 1.00 atm. Hvap for the liquid is 43.8 kJ/mol at 65° C.
43. Calculate w.
A) 27.7 J
B) –27.7 J
C) –2.81 103 J
D) 2.81 103 J
E) none of these
44. Calculate E.
A) 16.1 kJ
B) 41.0 kJ
C) 46.6 kJ
D) 71.5 kJ
E) none of these
45. When a student performs an endothermic reaction in a calorimeter, how (if any) does the calculated value of H differ from the
actual value if the heat exchanged with the calorimeter is not taken into account?
A) Hcalc is more negative because the calorimeter always absorbs heat from the reaction.
B) Hcalc is less negative because the calorimeter absorbs heat from the reaction.
C) Hcalc is more positive because the reaction absorbs heat from the calorimeter.
D) Hcalc is less positive because the reaction absorbs heat from the calorimeter.
E) Hcalc equals the actual value because the calorimeter does not absorb heat.
46. The standard enthalpy of formation of H2O(l) at 298 K is –285.6 kJ/mol. Calculate the change in internal energy for the
following process at 298 K:
H2(g) + 1/2 O2(g) H2O(l)
A) –283.1 kJ/mol
B) –281.9 kJ/mol
C) –285.6 kJ/mol
D) –289.3 kJ/mol
E) 283.1 kJ/mol
47. A bomb calorimeter has a heat capacity of 2.18 kJ/K. When a 0.176-g sample of gas with a molar mass of 28.0 g/mol was
burned in this calorimeter, the temperature increased by 2.12 K. Calculate the energy of combustion for 1 mol of this gas.
A) –1.29 102 kJ
B) –4.62 kJ
C) –2.63 101 kJ
D) –0.0291 kJ
E) –7.35 102 kJ
48. A calorimeter contains 95 g of water at 25.0°C. A 5.0-g sample of ice (at -5.0°C) is added to the water in the calorimeter, and
eventually all of the ice melts. Calculate the final temperature of the water. Assume no heat is lost to the calorimeter or the
surroundings.
A) 21.2°C
B) 20.7°C
C) 19.6°C
D) 17.5°C
E) none
49. The enthalpy of fusion of ice is 6.020 kJ/mol. The heat capacity of liquid water is 75.4 J/mol∞C. What is the smallest number of
ice cubes at 0∞C, each containing 1 mol of water, necessary to cool 500. g of liquid water initially at 20∞C to 0∞C?
A) 1
B) 7
C) 14
D) 15
E) 126
50. 75.0 mL of a pure liquid at 245 K is mixed with 100.0 mL of the same pure liquid at 365. K. What is the final temperature of the
mixture?
A) 295 K
B) 305 K
C) 314 K
D) 325 K
E) none of these
51. A calorimeter contains 142 g of water at 22.5°C. A 12-g sample of NaCl is added to the water in the calorimeter. After the
solid has dissolved, the temperature of the water is 21.4°C. Calculate the enthalpy of solution for dissolving sodium chloride.
Assume that no heat is lost to the calorimeter or the surroundings and that the specific heat of the solution is the same as that of
pure water.
A) 0.71 kJ/mol
B) 0.83 kJ/mol
C) 3.2 kJ/mol
D) 3.5 kJ/mol
E) 0.059 kJ/mol
52. A 1.00-g sample of the rocket fuel hydrazine, N2H4, is burned in a bomb calorimeter containing 1200. g of water. The
temperature of the water and the bomb calorimeter rises from 24.62°C to 28.16°C. Assuming the heat capacity of the empty
bomb calorimeter is 837 J/°C, calculate the heat of combustion of 1 mol of hydrazine in the bomb calorimeter. (The specific
heat capacity of water is 4.184 J/g•°C.)
A) –665 kJ
B) +20.7 kJ
C) –152 kJ
D) +47.4 kJ
E) –569 kJ
53. A 50.0-g sample of a metal is heated to 98.7°C and then placed in a calorimeter containing 395.0 g of water (c = 4.18 J/g°C) at
22.5°C. The final temperature of the water is 24.5°C. Which metal was used?
A) aluminum (C = 0.89 J/g°C)
B) iron (C = 0.45 J/g°C)
C) copper (C = 0.20 J/g°C)
D) lead (C = 0.14 J/g°C)
E) none of these
54. Calculate H° for the reaction C4H4(g) + 2H2(g) C4H8(g), using the following data:
H°combustion for C4H4(g) = –2341 kJ/mol
H°combustion for H2(g) = –286 kJ/mol
H°combustion for C4H8(g) = –2755 kJ/mol
A) –128 kJ
B) –158 kJ
C) 128 kJ
D) 158 kJ
E) none of these
55. At 25°C, the following heats of reaction are known:
2C2H2 + 5O2 4CO2 + 2H2O H = –2600.0 kJ
C + O 2 CO2 H = –394 kJ
2H2 + O2 2H2O H = –572 kJ
At the same temperature, calculate H for the following reaction:
2C + H 2 C2H2 H = ?
A) 226 kJ
B) -226 kJ
C) 2422 kJ
D) -2422kJ
E) none of these
56. Using Hess's law and equations 1-3 below, find H° at 25°C for the oxidation of C2H5OH(l).
A) 44 kJ
B) 632 kJ
C) -1367 kJ
D) -1742 kJ
E) none of these
57. Consider the following numbered processes:
1. A 2B
2. B C + D
3. E 2D
H for the process A 2C + E is
A) H1 + H2 + H3
B) H1 + H2
C) H1 + H2 – H3
D) H1 + 2H2 – H3
E) H1 + 2H2 + H3
A) –217.5 kJ/mol
B) –130.2 kJ/mol
C) +217.5 kJ/mol
D) –108.7 kJ/mol
E) none of these
59. Use the following table:
Reaction H° (kJ)
I. P 4(s) + 6Cl2(g) 4PCl3(g) -1225.6
II. P 4(s) + 5O 2(g) P 4O10(g) -2967.3
III. PCl 3(g) + Cl2(g) PCl5(g) -84.2
IV. PCl 3(g) + (1/2)O2(g) Cl3PO(g) -285.7
Calculate H for the combustion of 1 mol of methanol under standard conditions. Use the following standard enthalpies of
formation:
H°f for CH 3OH(l) = -238.5 kJ/mol
H°f for CO 2(g) = -393.5 kJ/mol
H°f for H2O(l) = -285.6 kJ/mol
A) +726.2 kJ/mol
B) -726.2 kJ/mol
C) +1452.4 kJ/mol
D) -1452.4 kJ/mol
E) none of these
67. The enthalpy of formation of an element in its standard state is
A) the enthalpy of its reaction with hydrogen.
B) the enthalpy of its reaction with oxygen.
C) determined by its melting point.
D) zero.
E) none of these
68. The heat combustion of acetylene, C2H2(g), at 25°C, is –1299 kJ/mol. At this temperature, H°f values for CO2(g) and H2O(l)
are –393 and –286 kJ/mol, respectively. Calculate H°f for acetylene.
A) 2376 kJ/mol
B) 625 kJ/mol
C) 227 kJ/mol
D) –625 kJ/mol
E) none of these
69. For the reaction
AgI(s) + (1/2)Br2(g) AgBr(s) + (1/2)I2(s), H° = –54.0 kJ
H°f for AgBr(s) = –100.4 kJ/mol
H°f for Br2(g) = +30.9 kJ/mol
The value of H°f for AgI(s) is
A) –123.5 kJ/mol
B) +77.3 kJ/mol
C) +61.8 kJ/mol
D) –77.3 kJ/mol
E) –61.8 kJ/mol
70. Using the following data, calculate the standard heat of formation of ICl(g) in kJ/mol.
H° (kJ/mol)
Cl2(g) 2Cl(g) 242.3
I 2 (g) 2I(g) 151.0
ICl(g) I(g) + Cl(g) 211.3
I 2(s) I2(g) 62.8
A) –211 kJ/mol
B) –14.6 kJ/mol
C) 16.8 kJ/mol
D) 245 kJ/mol
E) 439 kJ/mol
71. Using the information below, calculate H°f for PbO(s).
PbO(s) + CO(g) Pb(s) + CO2(g), H° = –131.4 kJ
H°f for CO2(g) = –393.5 kJ/mol
H°f for CO(g) = –110.5 kJ/mol
A) –151.6 kJ/mol
B) –283.0 kJ/mol
C) +283.0 kJ/mol
D) –372.6 kJ/mol
E) +252.1 kJ/mol
Use Hess's law to find the change in enthalpy at 25°C for the following equation:
CaC2(s) + 2H2O(l) C2H2(g) + Ca(OH)2(aq)
75. Consider the following standard heats of formation:
P4O10(s) = –3110 kJ/mol
H2O(l) = –286 kJ/mol
H3PO4(s) = –1279 kJ/mol
Calculate the change in enthalpy for the following process:
P4O10(s) + 6H2O(l) 4H3PO4(s)
76. Acetylene (C2H2) and butane (C4H10) are gaseous fuels. Determine the ratio of energy available from the combustion of a given
volume of acetylene to butane at the same temperature and pressure using the following data:
The change in enthalpy of combustion for C2H2(g) = –49.9 kJ/g.
The change in enthalpy of combustion for C4H10 = –49.5 kJ/g.
Answers
1. C 11. A 21. B 31. C 41. A 51. D 61. D 71. A
2. C 12. C 22. B 32. B 42. B 52. A 62. B 72. A
3. A 13. A 23. B 33. A 43. C 53. A 63. D
4. A 14. B 24. A 34. A 44. B 54. B 64. C
5. E 15. C 25. E 35. E 45. D 55. A 65. C
6. C 16. A 26. A 36. A 46. B 56. C 66. B
7. D 17. D 27. B 37. A 47. E 57. D 67. D
8. B 18. A 28. E 38. D 48. C 58. D 68. C
9. A 19. B 29. B 39. C 49. B 59. B 69. E
10. C 20. B 30. A 40. A 50. C 60. E 70. C