Gases
Introduction
We live in a solution of gases;
nitrogen, oxygen and other
gases surround and support
us. In this chapter we will
focus on the behavior of
5.1 Pressure
Properties of Gases
Gases are compressible
Gases uniformly fill any
container
Gases mix easily with other
Barometer
-
In 1643, Evangelista
Torricelli invented the
barometer, an instrument
for measuring
atmospheric pressure.
Atmospheric pressure
results from gravity’s pull
on air masses.
dish filled with mercury with a
closed tube
outside pressure causes
Manometer- instrument used for
measuring pressure
Gas pressure less than
atmospheric pressure
gas pressure = atm pressure –
h
Gas pressure greater than
atmospheric pressure
gas pressure= atm pressure +
h
The Manometer
mm Hg is also called torr
760mm Hg = 760 torr
= 1 atm
SI unit of pressure is
N/m2 or Pascal (Pa)
1 atm = 101,325 Pa or
101.325 kPa
Boyle’s Law
1
stquantitative study of gases, 1600s.
Pressure and volume are inversely related.
P
1= V
2P
1V
1= P
2V
2P
2V
1Ideal gas- gas that obeys Boyle’s law
We “Boyle” peas and vegetables
An
ideal
gas
is
expected to
have a
constant
value of PV,
as
CO
2shows the
largest
change in
PV, but this
Charles’ Law 1700’s
-volume of a gas is directly proportional to
Kelvin temperature
V
1= V
2**
Temp must be in
Kelvin!!!!!!
T
1T
2The volume of a gas at absolute zero is zero.
Notice how the balloon shrinks in the cold water and expands in the warm water.
A Charlie Brown
Avogadro’s
Law
-equal volumes of gases at the same
temperature and pressure contain
the same # of particles
-for a gas at constant temp. and
pressure, the volume is directly
Gay-Lussac’s Law
Pressure of a gas is directly proportional to
Kelvin temperature
P
1= P
2Temp must be in Kelvin!!!!!!
T
1T
2Gayle
drive s
a PT c ruise
Combined Gas Law
P
1
V
1
= P
2
V
2
T
1
T
2
Ideal Gas
Law
Combining Boyle’s, Charles’,
and Avogadro’s laws we get
PV= nRT.
R = 0.08206 L
.atm/K
.mol
(proportionality constant)
Most gases behave
We can use the ideal gas law for all gas law
problems by putting changing variables
on one side and the constant on the other.
Ex. If P&V change w/ others constant:
P
1V
1= nRT and P
2V
2= nRT
so P
1V
1= P
2V
2Ex. If V&T change with others constant:
V
1= nR and V
2= nR so V
1= V
2T
1P T
2P T
1T
2If the volume is held constant, then the
formula P
1V
1/T
1= P
2V
2/T
2shortens down to
P
1/T
1= P
2/T
2.
1.5atm = x atm
298K 725K
We use P
1V
1/T
1= P
2V
2/T
2and
solve for V
2.(45.6atm)(16.5L) = (1 atm)(x L)
(351K) (273K)
X = 585 L
Ex. A quantity of helium gas occupies a
volume of 16.5 L at 78
oC and 45.6 atm.
We will use PV = nRT and solve for n or moles so that
we can convert to mass.
(2.039 atm)(50.0L) = (n)(0.08206L.atm/mol.K)(296K)
n = 4.20 mol O2
4.20 mol O2 32.0g O2 = 134 g O2
Molar Volume = 22.42 L
of an ideal gas at STP
(Some gases behave
more ideally than
others.)
In this problem, we must first find the mol of hydrogen gas produced (this gas causes the pressure in the
balloon) and then convert to grams of CaH2. PV=nRT
(1.12 atm)(5.50L) = (n)(0.08206L.atm/mol.K)(288K)
N = 0.261 mol H2
0.261 mol H2 1 mol CaH2 42.1 g CaH2 = 5.49g CaH2
2 mol H2 1 mol CaH2
Ex. CaH
2reacts with H
2O to produce
H
2gas.
CaH
2(s)
+ 2H
2O
(l)
2H
2(g)
+ Ca
2+(aq)
+ 2OH
-(aq)
Assuming complete rxn with water,
how many grams of CaH
2are
required to fill a balloon to a total
pressure of 1.12 atm at 15
oC if its
First, we must write the balanced equation.
N2 + 3H2
2NH3
Now, we convert, using 1 mol=22.4L as a
conversion factor because this reaction is
occurring at STP.
115 g NH3 1 mol NH3 1 mol N2 22.4L
N2 = 75.8L N2
17.0g NH3 2 mol NH3 1 mol N2
n = mass so P = m R T
MW (MW)V
Since m/V = density (g/L),
P = dRT
MW
MW = dRT
P
“Molecular Weight Kitty Cat”
MW = dRT/P
d= mass/volume = 0.608g/0.750L = 0.811 g/L T = 35°C + 273.15 = 308 K
P = 385mmHg 1 atm = 0.507 atm 760 mm Hg
MW = [(0.811g/L)(0.08206L.atm/mol.K)(308
K)]/0.507 atm
MW = 40.4 g/mol
Dalton’s Law of Partial Pressures
For a mixture of gases in a container, the
total pressure exerted is the sum of the
pressures that each gas would exert if it
were alone.
P
tot= P
1+ P
2+ P
3+ …
P
tot= n
1RT + n
2RT + n
3RT +…
V V V
P
tot= n
total(RT)
(It doesn’t matter what the gas is.)-the ratio of the number of moles
of a given component in a mixture
to the total number of moles in the
mixture.
is used to symbolize mole fraction
1= n
1n
1+ n
2+ n
3+ …
The partial pressure of a particular
component of a gaseous mixture is
the mole fraction of that component
times the total pressure.
P
1=
1(P
total)
When gases are collected over
water, we must adjust for the
pressure of the water vapor.
In this problem, the total volume should be the sum of the partial pressures of each gas.
However, we must take into account the pressure of each gas as it fills the new container.
Therefore, we will use P1V1=P2V2 to find each sample’s partial pressure.
Oxygen (1.0atm)(0.20L)=(P2)(0.40L) P2 = 0.50 atm
Nitrogen (2.0atm)(0.10L)=(P2)(0.40L) P2 = 0.50 atm
Ptotal = PO2 + PN2 = 0.50 + 0.50 = 1.0 atm
Ex. If a 0.20 L sample of O
2at 0
oC and 1.0 atm
pressure and a 0.10 L sample of N
2at 0
oC and
2.0 atm pressure are both placed in a 0.40 L
container at 0
oC, what is the total pressure in
Kelvin temp. is an index of the
random motions of the particles
of a gas, with higher temp.
meaning greater motion.
KE (avg) = 3/2 RT
R = 8.3145 J/K mol
Units are J/mol
u
2= avg of the squares of the
particle velocities
= root mean square velocity =
u
rmsu
rms= where M = mass of
a mole of
gas in
kg
The units of u
rmsare m/s.
Root mean square
velocity
2
u
M
RT
)
/
3
At any given temp., lighter
molecules have higher root mean
square velocities.
Ex. Calculate the root mean square
velocity in m/s of O
2molecules at 27
oC.
s
m
kg
M
RT
u
rms483
.
6
/
KE = 3/2RT
KE = 3/2 (8.3145)300
=
3740 J
Calculate the avg. KE of
the same molecules.
Ex. Calculate the root mean square
Real gases have many collisions
between particles. The average
distance a particle travels
between collisions in a particular
gas sample is called the mean
free path. These collisions
produce a huge variation in
velocities. As temperature
A Plot of the Relative Number of O2
A Plot of the
Relative
Number of N
2Molecules That
Have a Given
Velocity at
Three
Effusion and
Diffusion
Diffusion- mixing of gases
Graham’s Law of Effusion
-The rate of effusion of a gas is
inversely proportional to the square
root of the mass of its particles
.
____
Rate of effusion for gas 1 =
MW
2Rate of effusion for gas 2
MW
1-diffusion rates can be
calculated the same way
Real gases
*No gas exactly follows the
ideal gas law.
*A real gas exhibits behavior
closest to ideal behavior at low
pressures and high
At high temperatures, there is less
interaction between particles because
they are moving too fast.
At high concentrations, gases have
much greater attractive forces between
particles. This causes particles to hit
At high pressure (small volume), the
volume of the particles becomes significant,
so that the volume available to the gas is
significantly less than the container
volume.
We can use the Van der Waals
equation to adjust for departures
from ideal conditions.
PV = nRT becomes:
[P
obs+ a(n/V)
2]V-nb = nRT
corrected corrected
pressure volume
a
= correction for pressure that takes into
b
= correction for the finite volume
of the gas molecules. It is a measure
of the actual volume occupied by the
gas molecules. It increases with an
increase in mass of the molecule or
in the complexity of the structure.
-major gases are N
2and O
2-see others in Table 5.4, pg 225
-heaviest gases are concentrated
closest to the surface
Chemistry
in the
Read about ozone layer protection.
Most air pollution centers around
NO, Nitric oxide, which is emitted
into the air from exhaust of engines.
NO + O
2
NO
2NO
2(g)
NO + O
O + O
2
O
3S (from coal) + O
2
SO
22SO
2+ O
2
2SO
3SO
3+ H
2O
H
2SO
4Read about scrubbers,
etc.
Ozone reacts with
unburned hydrocarbons in
polluted air to produce
irritating chemicals. This
process creates