WS 4.1 Key All gas molecules or atoms are always in constant

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WS 4.1 Key
1.
a) All gas molecules or atoms are always in constant, random motion. Collisions between molecules produce
pressure without a loss in total energy, (elastic collisions), KE is proportional to Temp.
b) Ideal gas molecules have negligible volume and gas molecules don’t attract to each other. NOTE: these
postulates are for Ideal Gases only.
πŸ‘
2. a) π‘²π‘¬π’‚π’—π’ˆ = 𝑹𝑻
πŸ‘π‘Ήπ‘»
π“œ
b) π’–π’“π’Žπ’” = √
3.
4.
5.
6.
𝒓𝒂𝒕𝒆𝒂
𝒓𝒂𝒕𝒆𝒃
= √π“œπ’ƒ
𝒓𝒂𝒕𝒆𝒂
𝒓𝒂𝒕𝒆𝒃
= √π“œπ’ƒ
(32𝑠)
4.67
8.
20𝑠
.48
π“œ
) (274𝐾) = 3415.41 𝐽/π‘šπ‘œπ‘™ with Sigfigs. 3420 J/mol
(πŸ‘)(πŸ–.πŸ‘πŸ 𝑱/π’Žπ’π’ 𝑲)(πŸπŸ•πŸ’π‘²)
.πŸŽπŸπŸŽπŸπŸ– π’Œπ’ˆ/π’Žπ’π’
= 581.80 π‘š/𝑠 with SigFigs 582 m/s
πŸ‘πŸ
= √πŸ’.𝟎 He effuses 2.8 times faster than O2
𝒓𝒂𝒕𝒆 𝒐𝒇 π‘―πŸ
𝒓𝒂𝒕𝒆 𝒐𝒇 π‘ͺπ‘ΆπŸ
𝒂
molβˆ™K
π’–π’“π’Žπ’” = √
𝒓𝒂𝒕𝒆 𝒐𝒇 𝑯𝒆
𝒓𝒂𝒕𝒆 𝒐𝒇 π‘ΆπŸ
𝒂
J
𝟐
πŸ’πŸ’.𝟎𝟏
H2 effuses 4.67 times faster than CO2
= √ 𝟐.𝟎𝟐
= 6.85𝑠
𝒓𝒂𝒕𝒆𝒂
𝒓𝒂𝒕𝒆𝒃
7. (
π“œ
πŸ‘
π‘²π‘¬π’‚π’—π’ˆ = (8.31
𝟐
π“œ
𝒓𝒂𝒕𝒆 𝒐𝒇 π‘΅π‘―πŸ‘
𝒓𝒂𝒕𝒆 𝒐𝒇 𝑯𝒆
= √π“œπ’ƒ
𝒂
πŸ’.πŸŽπŸŽπ’ˆ
NH3 compared to He: 0.48 times (slower of course)
= √πŸπŸ•.πŸŽπŸ’π’ˆ
) = πŸ’πŸ 𝒔𝒆𝒄
𝒓𝒂𝒕𝒆𝑯𝒆
π’“π’‚π’•π’†π’–π’π’Œπ’π’π’˜π’
π“œπ’ƒ
πŸ’.𝟎𝟎
=√
𝟏
𝟎.πŸπŸ“
π“œπ’ƒ
πŸ’.𝟎𝟎
=√
= πŸ”πŸ’ π’ˆ/π’Žπ’π’
πŸ‘π‘Ήπ‘»
π“œ
9. a) A is O2 and B is He. O2 is heavier and would have slower speeds compared to He. π’–π’“π’Žπ’” = √
πŸ‘π‘Ήπ‘»
π“œ
b) B is higher temperature. Hotter gas has greater speed than cooler gas. π’–π’“π’Žπ’” = √
10. 1.22 π‘Žπ‘‘π‘š ×
1.22π‘Žπ‘‘π‘š ×
1.22π‘Žπ‘‘π‘š ×
760π‘šπ‘šπ»π‘”
1π‘Žπ‘‘π‘š
101.325π‘˜π‘ƒπ‘Ž
1π‘Žπ‘‘π‘š
760π‘‡π‘œπ‘Ÿπ‘Ÿ
1π‘Žπ‘‘π‘š
= 927.2 π‘šπ‘šπ»π‘” (927𝑠𝑖𝑔𝑓𝑖𝑔)
= 123.62 π‘˜π‘ƒπ‘Ž (124𝑠𝑖𝑔𝑓𝑖𝑔)
= 927.2 π‘‡π‘œπ‘Ÿπ‘Ÿ (927𝑠𝑖𝑔𝑓𝑖𝑔)
11. 520π‘šπ‘šπ»π‘”
749π‘šπ‘šπ»π‘” − 670π‘šπ‘šπ»π‘” = 79π‘šπ‘šπ»π‘”
749π‘šπ‘šπ»π‘” + 103π‘šπ‘šπ»π‘” = 852π‘šπ‘šπ»π‘”
12. a) The piston would move upward to double the volume because the greater number of molecules exerts twice
the pressure.
b) The piston would move upward to double the volume because the faster moving molecules exert twice the
pressure.
c) The piston would move downward to halve the volume so that molecules are more crowded in order to
produce enough collisions to match the pressure.
13.
P
V
n
T
2.00 atm
1.00 L
1.500 mol
16.2 K
30.3 kPa
1.250 L
0.0152 mol
27oC
650 torr
11.2 L
0.333 mol
350 K
10.4 atm
585 mL
0.250 mol
295 K
14. a) 𝑃𝑉 = 𝑛𝑅𝑇
b) 0.382π‘šπ‘œπ‘™π‘‚2 ×
15.
π‘·πŸ π‘½πŸ
=
π’πŸ π‘»πŸ
𝑇2 =
16.
π‘š
𝑉
𝑃𝑉
(94.6π‘˜π‘ƒπ‘Ž)(10.0𝐿)
= (8.31)(298𝐾)
𝑅𝑇
32.0 𝑔 𝑂2
= 𝟏𝟐. 𝟐 π’ˆ π‘ΆπŸ
1 π‘šπ‘œπ‘™
𝑛=
π‘·πŸ π‘½πŸ
(πŸ•πŸ“πŸŽπ’•π’π’“π’“)(πŸ‘πŸ“πŸŽπ’Žπ‘³)
π’πŸ π‘»πŸ
π’πŸ (πŸπŸ–πŸ–π‘²)
(750π‘‘π‘œπ‘Ÿπ‘Ÿ)(450π‘šπΏ)(288𝐾)(𝑛1 )
(750π‘‘π‘œπ‘Ÿπ‘Ÿ)(350π‘šπΏ)(𝑛2 )
π‘ƒβˆ™β„³
given
π‘…βˆ™π‘‡
π‘š
π‘ƒβˆ™β„³
= π‘…βˆ™π‘‡
𝑉
=𝑑=
17. 𝑑 =
π‘ƒβˆ™β„³
π‘…βˆ™π‘‡
=
=
= 𝟎. πŸ‘πŸ–πŸ π’Žπ’π’
(πŸ•πŸ“πŸŽπ’•π’π’“π’“)(πŸ’πŸ“πŸŽπ’Žπ‘³)
π’πŸ π‘»πŸ
rearrange and solve for T2
= πŸ‘πŸ•πŸŽ. πŸ‘ 𝑲 This is really just Charles Law
the information, rearrange solving for molar mass(M)
π‘šπ‘…π‘‡
𝑃
=β„³
(1π‘Žπ‘‘π‘š)(17.04𝑔/π‘šπ‘œπ‘™)
(.0821)(273)
=
(4.93𝑔)(.0821)(400𝐾)
1.05π‘Žπ‘‘π‘š
= πŸπŸ“πŸ’. πŸπ’ˆ/π’Žπ’π’
= .76 𝑔/𝐿
18.
Total Pressure
Partial Pressure of He
Density
Average Kinetic energy per molecule
I and III are the same, then II
I, II, III
III, I, II
since T is same avg. KE is same for all
19. a. the number of moles of each gas.
n = PV/RT = (265/760)(1.0)/(0.0821)(298)
n = 0.014 mol
n = PV/RT = (800/760)(1.0)/(0.0821)(298)
Ne
n = 0.043 mol
n = PV/RT = (532/760)(0.5)/(0.0821)(298)
H2
n = 0.014 mol
b.
the total pressure after all stopcocks are opened.
P = nRT/V = (0.071)(0.0821)(298)/(2.5)
P = 0.695 atm (528 torr)
c.
the partial pressure of each gas.
PN2 = XN2Ptot = (0.014/0.071)(528 torr)
N2
PN2 = 104 torr
PNe = XNePtot = (0.043/0.071)(528 torr)
Ne
PNe = 320 torr
PH2 = XH2Ptot = (0.014/0.071)(528 torr)
H2
PH2 = 104 torr
N2
740 = PH2 + 32torr  PH2 = 708 torr
20. a) Ptot = PH2 + PH2O
b) 𝑃𝑉 = 𝑛𝑅𝑇 𝑛 =
𝑃𝑉
𝑅𝑇
=
(0.932π‘Žπ‘‘π‘š)(2.0𝐿)
(.0821)(303𝐾)
= πŸ•. πŸ“ × πŸπŸŽ−𝟐 π’Žπ’π’
21.
a) 𝑛 =
b) 𝑛 =
c)
𝒓𝒂𝒕𝒆𝒂
𝒓𝒂𝒕𝒆𝒃
𝑃𝑉
𝑅𝑇
𝑃𝑉
𝑅𝑇
=
=
(0.9489π‘Žπ‘‘π‘š).090𝐿)
(.0821)(298𝐾)
(0.0313π‘Žπ‘‘π‘š).090𝐿)
(.0821)(298𝐾)
πŸπŸ–.𝟎𝟐 π’ˆ/π’Žπ’π’
=√
𝟐.𝟎𝟐 π’ˆ/π’Žπ’π’
=
= πŸ‘. πŸ’πŸ— × πŸπŸŽ−πŸ‘ π’Žπ’π’ H2
= 𝟏. πŸπŸ“ × πŸπŸŽ−πŸ’ π’Žπ’π’ then convert to molecules: 6.92 x 1019 molecules H2O
H2 is 2.99 times faster
d) H2O shows hydrogen bonding which will causes it to deviate from ideal behavior, particularly at low temperatures and
high pressures.
22. a) PV=nRT 𝑷 =
𝒏𝑹𝑻
b) π‘ƒπ‘Ž = π‘‹π‘Ž βˆ™ π‘ƒπ‘‘π‘œπ‘‘π‘Žπ‘™
𝑽
=
(.πŸ”πŸŽπ’Žπ’π’)(.πŸŽπŸ–πŸπŸ)(πŸ‘πŸŽπŸŽπ‘²)
(πŸπŸŽπ‘³)
(π‘šπ‘œπ‘™π‘’ π‘“π‘Ÿπ‘Žπ‘π‘‘π‘–π‘œπ‘›)
π‘ƒπ‘Ž = (. 33) βˆ™ 74.9π‘˜π‘ƒπ‘Ž = πŸπŸ“π’Œπ‘·π’‚
= 𝟎. πŸ•πŸ‘πŸ—π’‚π’•π’Ž 𝒐𝒓 πŸ•πŸ’. πŸ—π’Œπ‘·π’‚
π‘‹π‘Ž =
π‘›π‘Ž
π‘›π‘‘π‘œπ‘‘π‘Žπ‘™
= .20π‘šπ‘œπ‘™
= .33
.60π‘šπ‘œπ‘™
23. π‘šπ‘œπ‘™π‘’ π‘“π‘Ÿπ‘Žπ‘‘π‘–π‘œπ‘› π‘œπ‘“ 𝐻𝑒 𝑖𝑠 .978 π‘Žπ‘›π‘‘ π‘šπ‘œπ‘™π‘’ π‘“π‘Ÿπ‘Žπ‘π‘‘π‘–π‘œπ‘› π‘œπ‘“ 𝑂2 𝑖𝑠 0.0218
(𝑛
+𝑛
)𝑅𝑇
π‘ƒπ‘‘π‘œπ‘‘π‘Žπ‘™ = 𝐻𝑒 𝑂2 = 12.099 atm
𝑉
PHe= XHe Ptotal = 0.978 x 12.099atm
= 11.8 atm
PO2= XO2 Ptotal = 0.0218 x 12.099atm
= 0.264 atm
24.
a) All have the same avg. KE because they are at the same temperature and temperature is a measure of
KE.
b) He because they have the lowest mass.
c) He because partial pressure is proportional to the number of moles of gas and the number of moles
increases with decreasing molar mass.
d) SO2 will deviate because they are the largest, have the greatest LDF interactions and they are also polar
molecules so they will have the strongest attractive forces.
e) SO2 because its polarity provides higher attractive forces.
f) Decreasing the temperature and increasing the pressure.
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