Sifat-Sifat Gas (Properties of Gases) : Kimia Dasar I (CH1101)
Sifat-Sifat Gas (Properties of Gases) : Kimia Dasar I (CH1101)
Sifat-Sifat Gas (Properties of Gases) : Kimia Dasar I (CH1101)
(Properties of Gases)
Kimia Dasar I (CH1101)
2018-2019
1
Outline:
1. A Molecular look at Gases
2. Pressure Measurement
3. Gas Laws
a. The simple gas law
b. Combining the gas law
4. Stoichiometry Using Gas Volumes
5. Ideal Gas Law
6. Dalton’s Law of Partial Pressure
7. Kinetic Theory of Molecular Gases
8. Real Gas
2
1. A Molecular Look at Gases
3
Molecular model of gases
Observations suggest
▪ A lot of space between molecules
▪ Molecules are moving at high speeds
▪ Molecules collide with walls of the container
▪ Molecules move faster at higher temperatures and
slower at lower temperatures
4
Elements that exist as gases at 250C
and 1 atmosphere
6
2. Pressure Measurement
The concept of Pressure
➢ Pressure is force per unit area
𝐹𝑜𝑟𝑐𝑒 (F)
𝑃𝑟𝑒𝑠𝑠𝑢𝑟𝑒(P) =
𝐴𝑟𝑒𝑎 (A)
➢ Earth exerts gravitational force on
everything with mass near it
Units of Pressure
1 pascal (Pa) = 1 N/m2
1 atm = 760 mmHg = 760 torr
1 atm = 101,325 Pa 7
How to measure atmosferic pressure
◼ Barometer
Instrument used to measure atmospheric pressure
8
How to measure atmosferic pressure
◼ Manometer
Instrument used to measure pressure in closed reaction
vessels.
(1). Open Ended Manometer
9
How to measure atmosferic pressure
• Pvacuum =0
• Pgas = Ph
11
Learning check:
12
Using liquids other than Mercury in
Manometers and Barometers
• If water ( = 1.00 gr/L) are used instead of
mercury ( = 13.6 g/mL) in the tube, the
correlation between them are:
14
Solution:
Ex. Converting mm Acetone to mm Hg - Solution
First convert mm acetone to mm Hg
◆ Boyle’s Law
• Studied on relationship
between gas Pressure
(P) and Volume (V).
• Work done at constant
temperature (T) and
constant number of
moles (n).
• When V decreases,
P increases
16
The simple gas law
◆ Charles’s Law
• He studied
correlation between
V and T, while P
and n are fixed.
• When T increase, so
does V
17
The simple gas law
◆ Gay-Lussac’s Law
• Worked on correlation between P and T,
while V and n are fixed.
• P is proportional to
absolute temperature
T(K)
18
Combining the gas law
▪ Ratio for fixed amount of moles
PV
=C
T
▪ OR can equate two sets of conditions to give
combined gas law
P1V1 P2V2
=
T1 T2
19
Combining the gas law
How Other Laws Fit into Combined Gas Law
P1V1 P2V2
=
T1 T2
Charles’ Law P1 = P2 V1 V2
=
T1 T2
Gay-Lussac’s V 1 = V2 P1 P2
Law =
T1 T2
20
Your Turn:
▪ What will be the final pressure of a
sample of nitrogen gas with a volume
of 1050 m3 at 730 mmHg and 25.0C if
it is heated to 75.0C and given a final
volume of 1250m3 ?
A. 716 mmHg
B. 720 mmHg
C. 724 mmHg
D. 740 mmHg
E. 746 mmHg
21
Avogadro’s Principle
▪ At constant P and T, equal V 's of gas contain
equal number of moles
▪ Volume of a gas is directly proportional to its
number of moles, n
▪ V is proportional to n (at constant P and T )
23
Learning Check:
Calculate the volume of ammonia formed by
the reaction of 20 L of hydrogen with excess
nitrogen.
N2(g) + 3H2(g) → 2NH3(g)
20 L H2 2 L NH3
= 13.3 L NH3
1 3 L H2
26
Learning Check:
How many liters of N2 (g) at 1 atm and
25 C are produced by the
decomposition of 150 gr of NaN3?
Reaction:
2 NaN3 (s) → 2Na(s) + 3N2 (g)
First determine the mole of N2
Mole ratio of NaN3 and N2 :
𝑚𝑜𝑙 𝑁𝑎𝑁3 2 𝑀𝑎𝑠𝑠𝑎 𝑁𝑎𝑁3 3
𝑚𝑜𝑙 𝑁2
=
3
, 𝑚𝑜𝑙 𝑁2 = 𝑀𝑚 𝑁𝑎𝑁3
𝑥
2
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5. Ideal gas
29
Ideal gas
nT
Va
P
nT nT
V = Constant x = R , R is the gas constant
P P
PV = nRT
31
Learning Check:
What is the volume of CO2 produced at 37 C and
1.00 atm when 5.60 g of glucose are used up in
the reaction:
C6H12O6 (s) + 6O2 (g) → 6CO2 (g) + 6H2O (l)
L•atm
0.187 mol x 0.0821 x 310.15 K
nRT mol•K
V= = = 4.76 L
P 1.00 atm
32
Your turn:
If 14 moles of N2O5 decompose into NO2 and O2
at 420 K in a 5 L container that can’t expand or
contract, after decomposition, how many times
greater is the pressure in the box than
atmospheric pressure (approx. 1 atm)?
35
Your turn:
36
6. Dalton’s Law of Partial Pressure
Ptotal = Pa + Pb + Pc +
• Pa, Pb and Pc are the partial pressures.
39
Partial Pressure
He O2
Pi = 1.0 atm Pf = PHe Pi = 1.0 atm Pf = PO2
Vi = 45 L Vf = 10 L Vi = 14 L Vf = 10 L
43
• First calculate pressure of each gas in 10 L tank (Pf )
using combined gas law
PiVi 1 atm 45 L
PHe = = = 4.5 atm
Vf 10 L
PiVi 1 atm 14 L
PO 2 = = = 1.4 atm
Vf 10 L
• Then use these partial pressures to calculate total
pressure
V
cancels, leaving
RT PA
cA =
PA + PB + PC + × × × + PZ
or
PA nA
cA = =
Ptotal n total
48
Learning Check:
❖ A sample of natural gas contains 8.24 moles
of CH4, 0.421 moles of C2H6, and 0.116 moles
of C3H8. If the total pressure of the gases is
1.37 atm, what is the partial pressure of
propane (C3H8)?
PA = XA PT PT = 1.37 atm
0.116
Xpropane = = 0.0132
8.24 + 0.421 + 0.116
50
Collecting gases over water
• Water vapor is present because molecules of water
escape from surface of liquid and collect in space
above liquid
• Molecules of water return to liquid
• When rate of escape = rate of return
• Number of water molecules in vapor state remains constant
• Gas saturated with water vapor = “Wet” gas
51
Vapor pressure
52
Learning Check
53
Solution:
a
1 𝑎𝑡𝑚
𝑃𝑡𝑜𝑡𝑎𝑙 = 738 𝑡𝑜𝑟𝑟 = 738 𝑡𝑜𝑟𝑟 𝑥 = 0.971 𝑎𝑡𝑚
760 𝑡𝑜𝑟𝑟
1 𝑎𝑡𝑚
𝑃𝑤𝑎𝑡𝑒𝑟 = 15.54 = 15.54 𝑡𝑜𝑟𝑟 𝑥 = 0.020 𝑎𝑡𝑚
760 𝑡𝑜𝑟𝑟
54
Solution:
b. Volume O2 gas at STP (1 atm, 0C)
𝑃1 = 0.951 𝑎𝑡𝑚 𝑃2 = 1 𝑎𝑡𝑚
𝑉1 = 300𝑚𝐿 = 0.3 𝐿 𝑉2 = ?
𝑇1 = 20𝐶 = 293𝐾 𝑇2 = 0𝐶 = 273𝐾
Using combined gas law formula
𝑃1 𝑉1 𝑃2 𝑉2 𝑃1 𝑉1 𝑇2
= 𝑉2 =
𝑇1 𝑇2 𝑇1 𝑃2
0.951𝑎𝑡𝑚 𝑥 0.3𝐿 𝑥 273𝐾
𝑉2 = = 𝟎. 𝟐𝟔𝟔 𝑳
293𝐾 𝑥 1𝑎𝑡𝑚 55
Your Turn
An unknown gas was collected by water
displacement. The following data was
recorded: T = 27.0 °C; P = 750 torr;
V = 37.5 mL; Gas mass = 0.0873 g;
PH2O(vap) = 26.98 torr
Determine the molecular weight of the gas.
A. 5.42 g/mol
B. 30.2 g/mol
C. 60.3 g/mol √
D. 58.1 g/mol
E. 5.81 g/mol 56
7. Kinetic Theory of Gases
➢ Specifically 3
KEave = RT
2
➢ As T increases, KEave increases
• Increase in number collisions with walls,
thereby increasing pressure
59
Kinetic Theory Explains Gas Laws
P and V (Boyle’s Law)
• For given sample of ideal gas at
given T
(n and T constant)
• If V decreases,
P increases
1
P = (nRT )
V
By kinetic theory of gases
• Decrease in V, means
gas particles hit wall more often
• Increase P
60
P and T (Gay-Lussac’s Law)
æ nR ö
P = çç ÷÷ T
èV ø
61
P and T (Gay-Lussac’s Law)
62
T and V (Charles’ Law)
æ nR ö
V = çç ÷÷ T
èP ø
63
T and V (Charles’ Law)
64
V and n (Avogadro’s Principle)
65
8. Real Gases
67
van der Waal’s equation for Real Gases
æ 2 ö
na
ççP +
è V 2
ø
( )
÷÷ V - nb = nRT
corrected P corrected V
n a
2
P + 2 (V − nb ) = nRT
V
corrected P
a — Pressure correction
• Indicates some attractions between
molecules
• Large a Means strong attractive forces
between molecules
• Small a Means weak attractive forces
between molecules
69
van der Waal’s equation for Real Gases
2
(V − nb ) = nRT
n a
P +
2
V
corrected V
b — Volume correction
• Deals with sizes of molecules
• Large b Means large molecules
• Small b Means small molecules
• Gases that are most easily liquefied have
largest van der Waal’s constants
70
Your Turn
For a given sample of gas, under which conditions are
actual pressures likely to deviate most from pressures
calculated based on the ideal gas law?
A. Weakly interacting molecules, high temperature,
large volumes
B. Weakly interacting molecules, high temperatures,
small volumes
C. Strongly interacting molecules, high temperatures,
small volumes
D. Strongly interacting molecules, low temperatures,
large volumes
E. Strongly interacting molecules, low temperatures,
small volumes 71
Solution:
Explanation:
▪ Strongly interacting molecules reduce the
pressure
▪ Molecules also interact with one another more
at low speed (i.e., low T)
▪ Molecules encounter one another more
often at low volume and thus can interact more
▪ These effects lead to lower actual pressures than
those predicted with the ideal gas law
72
Solution