CHAPTER 12
THE GASEOUS STATE OF MATTER
SOLUTIONS TO REVIEW QUESTIONS
1. In Figure 12.1, color is the evidence of diffusion; bromine is colored and air is colorless.If hydrogen and oxygen had been the two gases, this would not work because both gasesare colorless. Two ways could be used to show the diffusion. The change of densitywould be one method. Before diffusion the gas in the flask containing hydrogen would bemuch less dense. After diffusion, the gas densities in both flasks would be equal. Asecond method would require the introduction of spark gaps into both flasks. Beforediffusion, neither gas would show a reaction when sparked. After diffusion, the gases inboth flasks would explode because of the mixture of hydrogen and oxygen.
2. The pressure of a gas is the force that gas particles exert on the walls of a container. Itdepends on the temperature, the number of molecules of the gas and the volume of thecontainer.
3. The air pressure inside the balloon is greater than the air pressure outside the balloon. Thepressure inside must equal the sum of the outside air pressure plus the pressure exerted bythe stretched rubber of the balloon.
4. The major components of dry air are nitrogen and oxygen.
5.
6. The molecules of at 100°C are moving faster. Temperature is a measure of averagekinetic energy. At higher temperatures, the molecules will have more kinetic energy.
7. 1 atm corresponds to 4 L.
8. The pressure times the volume at any point on the curve is equal to the same value. Thisis an inverse relationship as is Boyle’s law.
9. If the volume of the cylinder would decrease (the piston would movedownward).
10. The pressure inside the bottle is less than atmospheric pressure. We come to thisconclusion because the water inside the bottle is higher than the water in the trough(outside the bottle).
T2 6 T1,
(PV = k)
H2
1 torr = 1 mm Hg
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11. The density of air is 1.29 g/L. Any gas listed below air in Table 12.3 has a density greaterthan air. For example:
12. Basic assumptions of Kinetic Molecular Theory include:
(a) Gases consist of tiny particles.(b) The distance between particles is great compared to the size of the particles.(c) Gas particles move in straight lines. They collide with one another and with the
walls of the container with no loss of energy.(d) Gas particles have no attraction for each other.(e) The average kinetic energy of all gases is the same at any given temperature. It
varies directly with temperature.
13. The order of increasing molecular velocities is the order of decreasing molar masses.
At the same temperature the kinetic energies of the gases are the same and equal toFor the kinetic energies to be the same, the velocities must increase as the molar
masses decrease.
14. Average kinetic energies of all these gases are the same, since the gases are all at thesame temperature.
15. Gases are described by the following parameters:
(a) pressure (c) temperature(b) volume (d) number of moles
16. An ideal gas is one which follows the described gas laws at all P, V and T and whosebehavior is described exactly by the Kinetic Molecular Theory.
17. Boyle’s law: ideal gas equation:If you have an equal number of moles of two gases at the same temperature the right sideof the ideal gas equation will be the same for both gases. You can then set PV for the firstgas equal to PV for the second gas (Boyle’s law) because the right side of both equationswill cancel.
18. Charles’ law: ideal gas equation:Rearrange the ideal gas equation to: V>T = nR>P PV = nRTV1>T1 = V2>T2,
PV = nRTP1V1 = P2V2,
1�2 mv2.
increasing molecular velocity
;99999999999999Rn, F2 , N2 CH4, He, H2
99999999999999:decreasing molar mass
O2, H2S, HCl, F2 , CO2.
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If you have an equal number of moles of two gases at the same pressure the right side ofthe rearranged ideal gas equation will be the same for both. You can set for the firstgas equal to for the second gas (Charles’ law) because the right side of bothequations will cancel.
19. A gas is least likely to behave ideally at low temperatures. Under this condition, thevelocities of the molecules decrease and attractive forces between the molecules begin toplay a significant role.
20. A gas is least likely to behave ideally at high pressures. Under this condition, themolecules are forced close enough to each other so that their volume is no longer smallcompared to the volume of the container. Attractive forces may also occur here andsooner or later, the gas will liquefy.
21. Equal volumes of and at the same T and P:
(a) have equal number of molecules (Avogadro’s law)
(b)
(c)
(d) average kinetic energies are the same (T same)
(e) rate the rate of (Graham’s Law of Effusion)
(f)
22. Behavior of gases as described by the Kinetic Molecular Theory.
(a) Boyle’s law. Boyle’s law states that the volume of a fixed mass of gas is inverselyproportional to the pressure, at constant temperature. The Kinetic Molecular Theoryassumes the volume occupied by gases is mostly empty space. Decreasing thevolume of a gas by compressing it, increases the concentration of gas molecules,resulting in more collisions of the molecules and thus increased pressure upon thewalls of the container.
density O2 = a32
2b (density H2) = 16(density H2)
density O2 = ¢mass O2
mass H2≤ (density H2) ¢ mass O2
density O2≤ = ¢ mass H2
density H2≤
volume O2 = volume H2
density H2 = ¢ mass H2
volume H2≤ density O2 = ¢ mass O2
volume O2≤
density O2 = 16 times the density of H2
O2H2 = 4 times
moles O2 = moles H2
mass O2 = 16 times mass of H2
O2H2
V>T V>T
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(b) Charles’ law. Charles’ law states that the volume of a fixed mass of gas is directlyproportional to the absolute temperature, at constant pressure. According to KineticMolecular Theory, the kinetic energies of gas molecules are proportional to theabsolute temperature. Increasing the temperature of a gas causes the molecules tomove faster, and in order for the pressure not to increase, the volume of the gasmust increase.
(c) Dalton’s law. Dalton’s law states that the pressure of a mixture of gases is the sumof the pressures exerted by the individual gases. According to the Kinetic MolecularTheory, there are no attractive forces between gas molecules; therefore, in a mixtureof gases, each gas acts independently and the total pressure exerted will be the sumof the pressures exerted by the individual gases.
23.
According to Avogadro’s Law, equal volumes of nitrogen and oxygen at the sametemperature and pressure contain the same number of molecules. In the reaction, nitrogenand oxygen molecules react in a 1:1 ratio. Since two volumes of nitrogen monoxide areproduced, one molecule of nitrogen and one molecule of oxygen must produce twomolecules of nitrogen monoxide. Therefore each nitrogen and oxygen molecule must bemade up on two atoms (diatomic).
24. We refer gases to STP because some reference point is needed to relate volume to moles.A temperature and pressure must be specified to determine the moles of gas in a givenvolume, and 0°C and 760 torr are convenient reference points.
25. Conversion of oxygen to ozone is an endothermic reaction. Evidence for this statement isthat energy is required to convert to
26. Chlorofluorocarbons, (Freons, and ), are responsible for damaging theozone layer. When these compounds are carried up to the stratosphere (the outer part ofthe atmosphere) they absorb ultraviolet radiation and produce chlorine free radicals thatreact with ozone and destroy it.
27. Heating a mole of gas at constant pressure has the following effects:
(a) Density will decrease. Heating the gas at constant pressure will increase its volume.The mass does not change, so the increased volume results in a lower density.
(b) Mass does not change. Heating a substance does not change its mass.
(c) Average kinetic energy of the molecules increases. This is a basic assumption of theKinetic Molecular Theory.
N2
(O3)
CCl2F2CCl3F,
O3.O2(286 kJ>3 mol O2)
1 vol + 1 vol ¡ 2 vol
N2(g) + O21g2 ¡ 2 NO1g2
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(d) Average velocity of the molecules will increase. Increasing the temperatureincreases the average kinetic energies of the molecules; hence, the average velocityof the molecules will increase also.
(e) Number of molecules remains unchanged. Heating does not alter the number ofmolecules present, except if extremely high temperatures were attained. Then, the
molecules might dissociate into N atoms resulting in fewer molecules.
28.An oxygen molecule contains 16 electrons.
Ozone molecule = O3Oxygen molecule = O2Oxygen atom = O
N2N2
N2
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CHAPTER 12
SOLUTIONS TO EXERCISES
1. (a)
(b)
(c)
2. (a)
(b)
(c)
3. (a)
(b)
(c)
(d)
4. (a)
(b)
(c)
(d) 10.67 kPa2a 1 atm
101.325 kPab = 0.0066 atm
1225 torr2a 1 atm
760 torrb = 0.296 atm
14250. cm Hg2a 1 atm
76 cm Hgb = 55.92 atm
162 mm Hg2a 1 atm
760 mm Hgb = 0.082 atm
15.00 kPa2a 1 atm
101.325 kPab = 0.0493 atm
1795 torr2a 1 atm
760 torrb = 1.05 atm
16000. cm Hg2a 1 atm
76 cm Hgb = 78.95 atm
128 mm Hg2a 1 atm
760 mm Hgb = 0.037 atm
1715 mm Hg2a101.325 kPa
760 mm Hgb = 95.3 kPa
1715 mm Hg2a 1013 mbar
760 mm Hgb = 953 mbar
1715 mm Hg2a 1 torr
1 mm Hgb = 715 torr
1715 mm Hg2¢ 14.7 lb/in.2
760 mm Hg≤ = 13.8 lb>in.2
1715 mm Hg2a 1 in. Hg
25.4 mm Hgb = 28.1 in. Hg
1715 mm Hg2a 1 atm
760 mm Hgb = 0.941 atm
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5. Change 625 torr to atmospheres and mm Hg.
(a)
(b)
6. Change 722 torr Hg to atmospheres and mm Hg.
(a)
(b)
7.
8.
9. Temperatures must be in Kelvin
(a)
(b)
10. Temperatures must be in Kelvin
(a)
(b)16.00 L21345 K2
248 K= 8.35 L
16.00 L21255 K2248 K
= 6.17 L
0.0°F = -18°C
(°C + 273)V1
T1=
V2
T2 or V2 =
V1T2
T1;
16.00 L21100. K2248 K
= 2.42 L
16.00 L21273 K2248 K
= 6.60 L
(°C + 273)V1
T1=
V2
T2 or V2 =
V1T2
T1;
11.7 atm21225 mL2115 mL
= 3.3 atmP2 =P1V1
V2
10.75 atm21521 mL2776 mL
= 0.50 atmP2 =P1V1
V2
1722 torr2(1 mm Hg/1 torr21635 mL2795 mm Hg
= 577 mL
1722 torr211 atm>760 torr21635 mL22.5 atm
= 241 mL
P1V1 = P2V2 or V2 =P1V1
P2.
1625 torr211mm Hg/1 torr2(525 mL)
455 mm Hg= 721 mL
1625 torr211 atm/760 torr2(525 mL)
1.5 atm= 288 mL
P1V1 = P2V2 or V2 =P1V1
P2.
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11. Use the combined gas law
12. Use the combined gas law
13. Use the combined gas law
14. Use the combined gas law
15. Use the combined gas law
16. Use the combined gas law
Change 765 torr to atmospheres.
17.
PN2= 721 torr - 19.8 torr = 701 torr
PH2O vapor = 19.8 torr
Ptotal = PN2+ PH2O vapor = 721 torr
1765 torr211 atm/760 torr211.5 L2(292 K)
11.5 atm212.5 L2 = 120 K (120 - 273) K = -150°C
P1V1
T1=
P2V2
T2 or T2 =
P2V2T1
P1V1
11.0 atm21775 mL21298 K21615 mL21273 K2 = 1.4 atm
P1V1
T1=
P2V2
T2 or P2 =
P1V1T2
V2T1
V2 =12.50 atm2122.4 L21268 K211.50 atm21300. K2 = 33.4 L
P1V1
T1=
P2V2
T2 or V2 =
P1V1T2
P2T1
V2 =10.950 atm211400. mL21275 K214.0 torr211 atm>760 torr21291 K2 = 2.4 * 105 L
P1V1
T1=
P2V2
T2 or V2 =
P1V1T2
P2T1
V2 =1740 mm Hg21410 mL21523 K21680 mm Hg21300. K2 = 7.8 * 102 mL
P1V1
T1=
P2V2
T2 or V2 =
P1V1T2
P2T1
V2 =1740 mm Hg21410 mL21273 K21760 mm Hg21300. K2 = 3.6 * 102 mL
P1V1
T1=
P2V2
T2 or V2 =
P1V1T2
P2T1
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18.
19.
20.
21.
To calculate the volume of dry methane, note that the temperature is constant, socan be used.
22. in propane
To calculate the volume of dry propane, note that the temperature is constant, socan be used.
23. 1 mol of a gas occupies 22.4 L at STP
24. 13.50 L2a 1 mol
22.4 Lb = 0.156 mol N2
11.75 L2a 1 mol
22.4 Lb = 0.0781 mol O2
V2 =P1V1
P2=1725 torr211.25 L21760. torr2 = 1.19 L C3H8
P1V1 = P2V2
PC3H8= 745 torr - 20.5 torr = 725 torr
PH2O vapor = 20.5 torr
C3H8Ptotal = PC3H8+ PH2O vapor
V2 =P1V1
P2=1696 torr212.50 L21760. torr2 = 2.29 L
P1V1 = P2V2
PCH4= 720. torr - 23.8 torr = 696 torr
PH2O vapor = 23.8 torr
Ptotal = PCH4+ PH2O vapor (Solubility of methane is being ignored.)
= 325 torr + 475 torr + 650. torr = 1450. torr = 1.450 * 103 torr
Ptotal = PH2+ PN2
+ PO2
= 200. torr + 600. torr + 300. torr = 1100. torr = 1.100 * 103 torr
Ptotal = PN2+ PH2
+ PO2
PN2= 705 torr - 23.8 torr = 681 torr
PH2O vapor = 23.8 torr
Ptotal = PN2+ PH2O vapor = 705 torr
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25. (a)
(b)
(c)
26. (a)
(b)
(c)
27.
28.
29.
30.
31. density of (from table 12.3)
32. density of (from table 12.3)
33. (a)
(b)
(c) d = ¢30.07 g C2H6
mol≤ a 1 mol
22.4 Lb = 1.34 g>L C2H6
d = ¢38.00 g F2
mol≤ a 1 mol
22.4 Lb = 1.70 g>L F2
d = a131.3 g Xe
molb a 1 mol
22.4 Lb = 5.86 g>L Xe
13.0 L210.716 g>L2 = 2.1 g CH4
CH4 gas = 0.716 g>L110.0 g2>13.17 g>L2 = 3.15 liters
Cl2 gas = 3.17 g>L11.00 L CH42a 1 mol
22.4 Lb ¢ 6.022 * 1023 molecules
mol≤ = 2.69 * 1022 molecules CH4
11.00 L NH32a 1 mol
22.4 Lb ¢ 6.022 * 1023 molecules
mol≤ = 2.69 * 1022 molecules NH3
1945 mL2a 1 L
1000 mLb a 1 mol
22.4 Lb a42.08 g
molb = 1.78 g C3H6
1725 mL2a 1 L
1000 mLb a 1 mol
22.4 Lb a17.03 g
molb = 0.551 g NH3
125.2 g2a 22.4 L
70.90 gb = 7.96 L Cl2
17.5 mol2a22.4 L
molb = 170 L C2H6
11.80 * 1024 molecules2a 22.4 L
6.02 * 1023 moleculesb = 67.0 L SO3
112.5 g2a 22.4 L
32.00 gb = 8.75 L O2
12.5 mol2a22.4 L
molb = 56 L CH4
16.02 * 1023 molecules2a 22.4 L
6.02 * 1023 moleculesb = 22.4 L CO2
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34. (a)
(b)
(c)
35. (a)
(b) Assume 1.00 mol of and determine the volume using the ideal gas equation,
36. (a)
(b) Assume 1.00 mol of and determine the volume using the ideal gas equation,
37. V =12.3 mol210.0821 L atm>mol K21300. K2
750 torr
760
torr
atm
= 57 L NeV =nRT
PPV = nRT
d =70.90 g
48.4 L= 1.46 g>L Cl2
= 48.4 L at 22°C and 0.500 atm
V =nRT
P=11.00 mol210.0821 L atm>mol K21295 K2
0.500 atm
PV = nRT.Cl2
d = ¢70.90 g Cl2
mol≤ a 1 mol
22.4 Lb = 3.165 g>L Cl2
d =38.00 g
24.6 L= 1.54 g>L F2
= 24.6 L at 27°C and 1.00 atm
V =nRT
P=11.00 mol210.0821 L atm>mol K21300. K2
1.00 atm
PV = nRT.F2
d = ¢38.00 g F2
mol≤ a 1 mol
22.4 Lb = 1.696 g>L F2
d = ¢56.10 g C4H8
mol≤ a 1 mol
22.4 Lb = 2.50 g>L C4H8
d = ¢44.01 g CO2
mol≤ a 1 mol
22.4 Lb = 1.96 g>L CO2
d = a222.0 g Rn
molb a 1 mol
22.4 Lb = 9.91 g>L Rn
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38.
39. When working with gases, the identity of the gas does not affect the volume, as long as thenumber of moles are known.
40. When working with gases, the identity of the gas does not affect the volume, as long as the number of moles are known.
41.
42.
43. The balanced equation is
(a)
(b)
44. The balanced equation is
(a) .
(b) (225 mL O2)a 1 L
1000 mLb a 1 mol
22.4 Lb a 2 mol H2O2
1 mol O2b = 0.0201 mol H2O2
(50.0 g H2O2)a 1 mol
34.02 gb a 1 mol O2
2 mol H2O2b a22.4 L
molb a 1000 mL
1 Lb = 1.65 * 104 mL O2
2 H2O2(aq) : 2H2O(l) + O2(g)
(525 mL H2) a 1 L
1000 mLb a 1 mol
22.4 Lb a 1 mol H2SO4
1 mol H2b = 0.0234 mol H2SO4
(52.7 g Zn) a 1 mol
65.39 gb a 1 mol H2
1 mol Znb a22.4 L
molb a 1000 mL
1 Lb = 1.81 * 104 mL H2
Zn(s) + H2SO4(aq) : H2(g) + ZnSO4(aq)
n =PV
RT=
10.500 atm215.20 L210.0821 L atm>mol K21250 K2 = 0.13 mol N2
PV = nRT
T =PV
nR=
14.15 atm210.250 L214.50 mol210.0821 L atm>mol K2 = 2.81 K
PV = nRT
V = 13.25 mol2a22.4 L
molb = 72.8 L
Total moles = mol N2 + mol HCl = 2.50 mol + 0.750 mol = 3.25 mol
V = 15.50 mol2a22.4 L
molb = 123 L
Total moles = mol H2 + mol CO2 = 5.00 mol + 0.500 mol = 5.50 mol
V =10.75 mol210.0821 L atm>mol K21298 K2
725 torr
760
torr
atm
= 19 L KrV =nRT
PPV = nRT
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45. The balanced equation is Remember that volume–volume relationships are the same as mole–mole relationshipswhen dealing with gases at the same T and P.
(a)
(b)
(c) Limiting reactant problem.
Oxygen is the limiting reactant. 20. L NO us formed.
46. The balanced equation is Remember that volume–volume relationships are the same as mole–mole relationshipswhen dealing with gases at the same T and P.
(a)
(b)
(c) Limiting reactant problem.
Oxygen is the limiting reactant. 12 L H2O is formed.
47. The balanced equation is
(0.525 kg KCl)a1000 g
1 kgb a 1 mol
74.55 gb a 3 mol O2
2 mol KClb a 22.4 L
1 molb = 237 L O2
2 KClO3(s) : 2 KCl(s) + 3 O2(g)
(15 L O2)a4 L H2O
5 L O2b = 12 L H2O
(15 L C3H8)a 4 L H2O
1 L C3H8b = 60. L H2O
(35 L C3H8)a 3 L CO2
1 L C3H8b a 1 mol
22.4 Lb a44.01 g
1 molb = 210 g CO2
(7.2 L C3H8)a 5 L O2
1 L C3H8b = 36 L O2
C3Hg(g) + 5 O2(g) : 3 CO2(g) + 4 H2O(g)
(25 L NH3)a 4 L NO
5 L NH3b = 25 L NO
(25 L O2)a4 L NO
5 L O2b = 20. L NO
(25 L NH3)a6 L H2O
4 L NH3b a 1 mol
22.4 Lb a 18.02 g
1 molb = 30. g H2O
(2.5 L NH3)a 5 L O2
4 L NH3b = 3.1 L O2
4 NH3(g) + 5 O2(g) : 4 NO(g) + 6 H2O(g)
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48. The balanced equation is
49. Like any other gas, water in the gaseous state occupies a much larger volume than in theliquid state.
50. During the winter the air in a car’s tires is colder, the molecules move slower and thepressure decreases. In order to keep the pressure at the manufacturer’s recommended psiair needs to be added to the tire. The opposite is true during the summer.
51. (a) the pressure will be cut in half
(b) the pressure will double
(c) the pressure will be cut in half
(d) the pressure will increase to 3.7 atm or 2836 torr
52.
P
(a)
V
T
(c)
P
T
(b)
V
n
(d)
V
P = 3.7 atm a760 torr
1 atmb = 2.8 * 103 torr
P =11.5 mol210.0821 L atm>mol K21303 K2
10. L= 3.7 atm
PV = nRT P =nRT
V
= 1.12 * 103 L CO2
(1.50 kg C6H12O6)a1000 g
1 kgb a 1 mol
180.16 gb a 6 mol CO2
1 mol C6H12O6b a 22.4 L
1 molb
C6H12O6(s) + 6 O2(g) : 6 CO2(g) + 6 H2O(l)
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53. The can is a sealed unit and very likely still contains some of the aerosol. As the can isheated, pressure builds up in it eventually causing the can to explode and rupture withpossible harm from flying debris.
54. One mole of an ideal gas occupies 22.4 liters at standard conditions. (0°C and 1 atmpressure)
55. Solve for volume using
(a)
(b)
(c)
has the greatest volume
56. Assume 1 mol of each gas
(a)
(b) Assume 25°C and 1 atm pressure
d = a30.07 g
molb a 1 mol
24.5 Lb = 1.23 g>L C2H6
C2H6 = 30.07 g>mol
V1at 25°C2 = 122.4 L2a298 K
273 Kb = 24.5 L
d = a146.1 g
molb a 1 mol
22.4 Lb = 6.52 g>L SF6
SF6 = 146.1 g>mol
4.2 g NH3
V =121 g SO32a 1 mol
80.07 gb a 0.0821 L atm
mol Kb(328 K)
110 kPa
101.3
kPa
atm
= 6.5 L SO3
V =14.2 g NH32a 1 mol
17.03 gb a 0.0821 L atm
mol Kb(262 K)
0.65 atm= 8.2 L NH3
V =10.2 mol Cl2210.0821 L atm>mol K21321 K2
180 cm>76 cm2 atm= 5 L Cl2
PV = nRT
V = 22.4 L
11.00 atm21V2 = 11.00 mol210.0821 L atm>mol K21273 K2PV = nRT
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(c) He at and 2.15 atm
has the greatest density
57. (a) Empirical formula. Assume 100 g starting material
(b) Molecular formula. (molar mass)
(c)
58.
(a)
(b)
10.052 mol N22¢28.02 g N2
mol≤ = 1.5 g N2
mol N2 = 0.085 mol - 0.020 mol O2 - 0.013 mol CO2 = 0.052 mol
= 0.085 mol -0.65 g O2
32.00 g>mol-
0.58 g CO2
44.01 g>mol
mol N2 = total moles - mol O2 - mol CO2
n = 0.085 mol (total moles)
a 1790 torr211 atm2760 torr
b12.0 L2 = 1n210.0821 L atm>mol K21298 K2PV = nRT
H
C H Lewis structureH
H
H
C
H
Valence electrons = 2142 + 6 = 14
30. g>mol
15.03 g>mol= 2; Molecular formula is C2H6
a 2.01 g
1.5 Lb a22.4 L
molb = 30. g>mol
Empirical mass = 12.01 g + 3.024 g = 15.03 g>mol
Empirical formula = CH3
19.8
6.66= 2.97
20.0 g H
1.008 g>mol= 19.8 mol H
6.66
6.66= 1
80.0 g C
12.01 g>mol= 6.66 mol C
SF6
d = a4.003 g
molb a 1 mol
7.37 Lb = 0.543 g>L He
V =11 mol210.0821 L atm>mol K21193 K2
2.15 atm= 7.37 L
-80°C
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(c)
59.Calculate the moles of and to find the limiting reactant.
CO:
Limiting reactant is CO
will react with 0.019 mol CO.
60.
61. (a) Assume atmospheric pressure of to begin with.
Total pressure in the
n = 0.18 mol air
128 lb>in.22¢ 1 atm
14.7 lb>in.2≤12.24 L2 = 1n210.0821 L atm>mol K21293 K2
PV = nRTball = 14.7 lb>in.2 + 13 lb>in.2 = 28 lb>in.2
14.7 lb>in.2
T =11.3 * 109 atm211.0 L212.0 g>mol210.0821 L atm>mol K211.4 * 103 g2 = 2.3 * 107 K
11.3 * 109 atm211.0 L2 = ¢ 1.4 * 103 g
2.0 g>mol≤10.0821 L atm>mol K21T2
¢1.4 g
cm3 ≤ ¢ 1000 cm3
L≤ = 1.4 * 103 g>L
PV = nRT or PV = a g
molar massbRT
10.019 mol CO2¢2 mol CO2
2 mol CO≤ a 22.4 L
molb = 0.43 L CO2 = 430 mL CO2
0.0095 mol O2
mol CO = 0.019 mol
a800 mm Hg * 1 atm
760 mm Hgb10.500 L2 = 1n210.0821 L atm>mol K21333 K2
mol O2 = 0.038 mol
11.8 atm210.500 L O22 = 1n210.0821 L atm>mol K21288 K2O2:
PV = nRTCOO2
2 CO + O2 ¡ 2 CO2
PN2= 1790 torr2¢ 0.051 mol N2
0.085 mol≤ = 4.7 * 102 torr
PCO2= 1790 torr2¢0.013 mol CO2
0.085 mol≤ = 1.2 * 102 torr
PO2= 1790 torr2¢ 0.020 mol O2
0.085 mol≤ = 1.9 * 102 torr
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(b) mass of air in the ball
(c) Actually the pressure changes when the temperature changes. Since pressure isdirectly proportional to moles we can calculate the change in moles required tokeep the pressure the same at 30°C as it was at 20°C.
of air required to keep the pressure the same at 30°C.
0.01 mol air must be allowed to escape from the ball.
or 0.3 g air must be allowed to escape.
62. Use the combined gas laws to calculate the bursting temperature
63. To double the volume of a gas, at constant pressure, the temperature (K) must be doubled.
64. at 22°C and 740 torr
after change in temperature (P constant)
after change in pressure (T constant)
Since temperature is constant,
torr (pressure to change 2 V to V)P2 = 1740 torr2a2 V
Vb = 1.5 * 103
P1V1 = P2V2 or P2 =P1V1
V2
V = volume
2 V = volume
V = volume
T2 = 21300. K2 = 600. K = 327°C
T2 = 2 T1 T2 =2 V1T1
V1 V1
T1=
2 V1
T2
V2 = 2 V1 V1
T1=
V2
T2
T2 =P2V2T1
P1V1=176 cm212.00 L21293 K2165 cm211.75 L2 = 392 K 1119°C2
T2 = T2 T1 = 20°C 1293 K2 V2 = 2.00 L V1 = 1.75 L
P2 = 1.00 atm (76 cm) P1 = 65 cmP1V1
T1=
P2V2
T2
(T2).
10.01 mol air2a29 g
molb = 0.29 g
(0.18 - 0.17)
n = 0.17 mol
128 lb>in.22¢ 1 atm
14.7 lb>in.2≤12.24 L2 = 1n210.0821 L atm>mol K21303 K2
PV = nRT
m = 10.18 mol2a29 g
molb = 5.2 g air
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65. Volume is constant, so or
66. The volume of the tires remains constant (until they burst), so
or
67. Use the combined gas laws.
or
68. Use the combined gas law or
First calculate the volume at STP.
At STP, a mole of any gas has a volume of 22.4 L
Each molecule of contains 3 atoms, so:
69. Pressure varies directly with absolute temperature.
T2 = 212°F = 100°C = 373 K
T1 = 25°C + 273 = 298 KP2 =P1T2
T1
P1
T1=
P2
T2
17.39 * 1021 molecules2a 3 atoms
1 moleculeb = 2.22 * 1022 atoms
N2O
10.275 L2a 1 mol
22.4 Lb ¢6.022 * 1023 molecules
1 mol≤ = 7.39 * 1021 molecules
V2 =1400. torr21600. mL21273 K2
1760. torr21313 K2 = 275 mL = 0.275 L
V2 =P1V1T2
P2T1
P1V1
T1=
P2V2
T2
P2 =11.00 atm21800. mL21303 K2
1250. mL21273 K2 = 3.55 atm
P1 and T1 are at STPP2 =P1V1T2
V2T1
P1V1
T1=
P2V2
T2
T2 =144 psi21295 K2
30. psi= 433 K = 160°C = 320°F
71.0°F = 21.7°C = 295 K
T2 =T1P2
P1;
P1
T1=
P2
T2
T2 =1500. torr21295 K2
700. torr= 211 K = -62°C
T2 =T1P2
P1;
P1
T1=
P2
T2
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At 212°F the tire pressure is
The tire will not burst.
70. A column of mercury at 1 atm pressure is 760 mm Hg high. The density of mercury is13.6 times that of water, so a column of water at 1 atm pressure should be 13.6 times ashigh as that for mercury.
71. Use the ideal gas equation
Change to atmosphere
72. The conversion is:
73. First calculate the moles of gas and then convert moles to molar mass.
74. The conversion is:
a1.78 g
Lb a22.4 L
molb = 39.9 g>mol (molar mass)
g>L ¡ g>mol
1.08 g
0.0250 mol= 43.2 g>mol (molar mass)
10.560 L2a 1 mol
22.4 Lb = 0.0250 mol
11.00 m32a100 cm
1 mb3¢ 1 mL
1 cm3 ≤ a 1 L
1000 mLb a 1 mol
22.4 Lb = 44.6 mol Cl2
m3 ¡ cm3 ¡ mL ¡ L ¡ mol
n =(150. atm)(55 L)
a0.0821 L # atm
mol # Kb(300. K)
= 3.3 * 102 mol O2
12.20 * 103 lb>in.22¢ 1 atm
14.7 lb>in.2≤ = 150. atm
2.20 * 103 lb>in.2
n =RT
PVPV = nRT
1760 mm2113.62 = 1.03 * 104 mm 133.8 ft2
40. lb>in.2
P2 =132 lb>in.221373 K2
298 K= 40. lb>in.2
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75.
(a)
(b)
The molar mass for is 16.04 g/mol
(c) but where M is the molar mass and g is the grams of the gas.
Thus, To determine density,
Solving for produces
(d) Since from part (c), solve for M (molar mass)
76.
is the limiting reactant. forms, no moles remain. According to the equation, 2.0 mol HF yields Therefore,
The flask contains and 3.0 mol HF when the reaction is complete.
The flask contains 4.0 mol of gas.
77. 18.30 mol Al2¢3 mol H2
2 mol Al≤ a22.4 L
molb = 279 L H2 at STP
P =nRT
V=14.0 mol210.0821 L atm>mol K21273 K2
10.0 L= 9.0 atm
1.0 mol C2H4F2
5.0 mol HF - 2.0 mol HF = 3.0 mol HF unreacted1.0 mol C2H4F2.
C2H21.0 mol C2H4F2C2H2
15.0 mol HF2¢1 mol C2H4F2
2 mol HF≤ = 2.5 mol C2H4F2
1.0 mol C2H2 ¡ 1.0 mol C2H4F2
C2H21g2 + 2HF1g2 ¡ C2H4F21g2
M =dRT
P=12.58 g>L210.0821 L atm>mol K21300. K2
1.00 atm= 63.5 g>mol (molar mass)
d =g
V=
PM
RT
d =g
V=
14.00 atm2144.01 g>mol210.0821 L atm>mol K21253 K2 = 8.48 g>L CO2
g
V=
PM
RT.
g
VPV =
gRT
M
d = g>V.PV =gRT
M.
n =g
MPV = nRT,
116.04 g>mol210.513 mol2 = 8.23 g CH4
CH4
n =PV
RT=
10.789 atm2116.0 L210.0821 L atm>mol K21300. K2 = 0.513 mol CH4
V =nRT
P=10.510 mol210.0821 L atm>mol K21320. K2
1.6 atm= 8.4 L H2
PV = nRT
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78. According to Graham’s Law of Effusion, the rates of effusion are inversely proportionalto the molar mass.
Helium effuses 2.646 times faster than nitrogen.
79. (a) According to Graham’s Law of Effusion, the rates of effusion are inverselyproportional to the molar mass.
Helium effuses twice as fast as
(b)
The gases meet 66.7 cm from the helium end.
80. Assume 100. g of material to start with. Calculate the empirical formula.
C
H
The empirical formula is To determine the molecular formula, the molar mass must be known.
The empirical formula mass is 14.0
Therefore, the molecular formula is
81. Determine the limiting reactant
110.0 mol CO2¢2 mol CO2
2 mol CO≤ = 10.0 mol CO2 (from CO)
2 CO1g2 + O21g2: 2 CO21g2(CH2)4 = C4H8
56.0
14.0= 4
a2.50 g
Lb a22.4 L
molb = 56.0 g>mol (molar mass)
CH2.
14.2
7.14= 1.99 mol 114.3 g2a 1 mol
1.008 gb = 14.2 mol
7.14
7.14= 1.00 mol 185.7 g2a 1 mol
12.01 gb = 7.14 mol
x = 66.7 cm
3x = 200
x = 21100 - x2D = distance traveledDHe = 2 DCH4
100 - x = distance CH4 travels
x = distance He travels
CH4.
rate He
rate CH4= A16.04
4.003= 24.007 = 2.002
rate He
rate N2= Amolar mass N2
molar mass He= A28.02
4.003= 27.000 = 2.646
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CO: the limiting reactant, in excess, unreacted.
(a) 10.0 mol CO react with
and are present, no CO will be present.
(b)
82.
First calculate the moles of produced. Then calculate the grams of required toproduce the Then calculate the %
83. Assume 1.00 L of air. The mass of 1.00 L of air is 1.29 g.
84. Each gas behaves as though it were alone in a 4.0 L system.
(a) After expansion:
(b) Ptotal = PH2+ PCO2
= 110 torr + 13 torr = 120 torr (2 sig. figures)
P2 =P1V1
V2=150. torr211.0 L2
4.0 L= 13 torrFor H2
P2 =P1V1
V2=1150. torr213.0 L2
4.0 L= 1.1 * 102 torrFor CO2
P1V1 = P2V2
d =m
V=
1.29 g
1.8 L= 0.72 g>L
V2 =P1V1T2
P2T1=1760 torr211.00 L21290. K21450 torr21273 K2 = 1.8 L
P1V1
T1=
P2V2
T2
a0.90 g
1.20 gb11002 = 75% KClO3 in the mixture
10.011 mol O22¢2 mol KClO3
3 mol O2≤ a122.6 g
molb = 0.90 g KClO3 in the sample
10.25 L O22a 1 mol
22.4 Lb = 0.011 mol O2
KClO3.O2.KClO3O2
2 KClO31s2 ¢
" 2 KCl1s2 + 3O21g2
P =nRT
V=113 mol210.0821 L atm>mol K21273 K2
10. L= 29 atm
3.0 mol O210.0 mol CO2
5.0 mol O2
3.0 mol O2O2:
18.0 mol O22¢2 mol CO2
1 mol O2≤ = 16 mol CO2 (from O2)
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85.
Gas cylinders have constant volume, so pressure varies directly with temperature.
86. You can identify the gas by determining its density.
volume of gas: Charles law problem. Correct volume to 273 K
gas is chlorine (see Table 12.3)
d =m
V=
1.200 g
0.3785 L= 3.170 g>L
V2 =V1T2
T1=10.4478 L21273 K2
323 K= 0.3785 L
V1
T1=
V2
T2
mass of gas = 1.700 g - 0.500 g = 1.200 g
P2 =P1T2
T1=140.0 atm21450. K2
298 K= 60.4 atm
T2 = 25°C + 152°C = 177°C = 450. K T1 = 25°C = 298 K
V2 = 50.0 L V1 = 50.0 L
P2 = P2 P1 = 40.0 atm
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