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Density Variation
D = m/v = g/L
MP = dRT
R
universal gas law constant
.0821 atm•L/K•mol
Ideal Gas Law
R = PV/nT or PV = nRT
Combined Gas Law
VP/T = VP/T (changed over time)
Avogadro’s Law
V/n = V/n (changed over time)
Direct Relationship
^n, ^collisions, ^P, ^V (flexible container)
Avg. KE is the same in 2 gases if
Temperature is constant
if Volume is = at STP
The number of moles is =
(avogadro’s law)
a
attractive forces between particles (real gas)
b
the volume of the gas particle itself (real gas)
Van der Waals Equation
\left\lbrack P+a\left(\frac{n}{V}\right)^2\rbrack\right.\cdot\left(V-nb\right)=nRT
Attractive Forces (T)
Intermolecular attractive forces tend to pull the particles toward one another, significantly reducing space
Attractive Forces (P)
High pressure creates more opportunities for collisions between particles
Real gases acting like ideal gases
Low pressure and high temperatures
Diffusion
the mixing of gases
the rate of diffusion = the rate of the mixing gases
Effusion
the passage of a gas through a tiny orifice (hole) into a evacuated chamber
Graham’s Law of Effusion
“graham cracker”
\frac{Rate_{a}}{Rate_{b}} = \sqrt{\frac{M_{b}}{M_{a}}}
Gay-Lussac’s Law
P/T = P/T (changed over time)
Direct Relationship in kelvin!!
^T, ^KE, ^collisions, ^P (rigid container)
Charles’ Law
V/T = V/T (changed over time)
Direct Relationship *KELVIN!!!*
^T, ^KE, ^collisions, ^P, ^V (increasing volume keeps pressure =)
(flexible container)
Boyle’s Law
VP = VP
Inverse Relationship
vV, ^collisions, ^P
Root Mean Square Velocity
u=\sqrt{\frac{3RT}{M}}
Collecting gas over water
Pgas(dry) = Ptotal - Ph2o
Mole fractions
X = n/n(total)
X = P/P(total)
Dalton’s Law
Ptotal = Pgas(a) + Pgas(b) + …
STP
V = 22.4L
T = 0*C = 273K
P = 1 atm = 760mmHg
Molar mass variation
n = m/M
PV = nRT \rightarrow PV = mRT/M
Density variation
d = m/V
d = MP/RT or MP = dRT
Kinetic Molecular Theory (KMT) 1
Gases are mostly empty space
Kinetic Molecular Theory (KMT) 2
Gases move rapidly and randomly in all directions and exert pressure in their collisions.
Kinetic Molecular Theory (KMT) 3
Gas particles are assumed to act independently of each other
Kinetic Molecular Theory (KMT) 4
the avg. KE of gas particles is assumed to be directly proportional to Kelvin temp. (KEave \alpha T)
\overline{u^2}
the average of the squares of the particle velocities
Kinetic Energy
KE = ½ m \overline{u^{}}^2
KEavg = 3/2 RT