Kinetic Molecular TheoryEdit
Ideal gases don't exist, but if they did, they would fit the following descriptions:
 Full of tiny particles that are far apart
 Neither attract nor repel each other
 Are constantly and randomly moving, creating pressure
 Do not lose energy when colliding.
PressureEdit
Pressure is measured with a barometer (for atmospheric pressure) or a manometer (for sealed containers of gases).
Gas LawsEdit
As the result of many different scientists and experiments, several gas laws have been discovered. These laws relate the various state variables of a gas.
 State Variables of a Gas
 Pressure (P)
 Volume (V)
 Temperature (T)
 Molar mass (n)
These gas laws can be used to compare two different gases, or determine the properties of a gas after one of its state variables have changed.
Avogadro's Law states that equal volumes of all ideal gases (at the same temperature and pressure) contain the same number of molecules.  
Boyle's Law states that equal pressure is inversely proportional to volume (when temperature is constant).  
Charles's Law states that volume is proportional to temperature (when pressure is constant). Remember that temperature must be measured in Kelvin.  
GayLussac's Law states that pressure is proportional to temperature (when volume is constant). 
Combined Gas LawEdit
Combining Charles's Law, Boyle's Law, and GayLussac's Law gives us the combined gas law.
For a gas with constant molar mass, the three other state variables are interrelated.  
The Combined Gas Law can be used for comparisons between gases. 
Ideal Gas LawEdit
When Avogadro's Law is considered, all four state variables can be combined into one equation. Furthermore, the "constant" that is used in the above gas laws becomes the Universal Gas Constant (R).
To better understand the Ideal Gas Law, you should first see how it is derived from the above gas laws.
and  This is simply a restatement of Avogadro's Law and the Combined Gas Law. 
We can now combine the laws together.  
Let R be a constant, and write the proportion in the form of an equation.  
Rearranging the fraction gives one form of the ideal gas law. 
The ideal gas law is the most useful law, and it should be memorized. If you know the ideal gas law, you do not need to know any other gas laws, for it is a combination of all the other laws. If you know any three of the four state variables of a gas, the unknown can be found with this law. If you have two gases with different state variables, they can be compared.
There are three ways of writing the ideal gas law, but all of them are simply algebraic rearrangements of each other.
This is the most common form.  
This form is useful for predicting the effects of changing a state variable. To maintain a constant value of R, an change in the numerator must result in a proportional change in the denominator, and vice versa. If, for example, the pressure is decreased in a constantvolume container, you can use this form to easily predict that the temperature must decrease.  
Because R is the same constant for all gases, this equation can be used to relate two gases to each other. 
;Rules for Using the Ideal Gas Law

Kinetic Molecular TheoryEdit
The Kinetic Molecular Theory attempts to explain the gas laws. It describes the behavior of microscopic gas molecules to explain the macroscopic behavior of gases. According to this theory, an ideal gas is composed of continually moving molecules of negligible volume. The molecules move in straight lines unless they collide into each other or the walls of their container.
The pressure of the gas on the container is explained as the force the molecules exert on the walls during a collision. Pressure is equal to the average force of collisions divided by the total surface area of the container.  
The temperature of the gas is proportional to the average kinetic energy of the molecules. denotes the average kinetic energy of the molecules, and is the Boltzman constant (1.388 x 10^{23}). 
The gas laws are now explained by the microscopic behavior of gas molecules:
 Boyle's Law: The pressure of a gas is inversely proportional to its volume. A container's volume and surface area are obviously proportional. Based on the pressure equation, an increase in volume (and thus surface area) will decrease pressure.
 Charles' Law: the volume of a gas is proportional to its temperature. As the volume (and surface area) increases, the pressure will decrease unless the force also increase. When pressure is constant, the volume and temperature must be proportional. The temperature equation above explains why: the energy of the molecules (and their collision force) is proportional to temperature.
 GayLussac's Law: The temperature of a gas is directly proportional to its pressure. An increase in temperature will increase the kinetic energy of the molecules (shown by the temperature equation). Greater kinetic energy causes the molecules to move faster. Their collisions with the container will have more force, which increases pressure.
 Avogadro's Law: Equal volumes of all ideal gases (at the same temperature and pressure) contain the same number of molecules. According to the Kinetic Molecular Theory, the size of individual molecules is negligible compared to distances between molecules. Even though different gases have different sized molecules, the size difference is negligible, and the volumes are the same.
Derivation of Ideal Gas LawEdit
Suppose there are molecules, each with mass , in a cubic container with side length . Even though the molecules are moving in all directions, we may assume, on average, that one third of the molecules are moving along the xaxis, one third along the yaxis, and one third along the zaxis. We may assume this because the motion of the molecules is random, so no direction is preferred.  
Suppose the average speed of the molecules is . Let a specific wall of the container be labeled A. Because the collisions in Kinetic Molecular Theory are perfectly elastic, the speed after a collision is . Therefore, the average change in momentum (the product of mass and velocity) per collision is .
Each molecule, on average, travels a distance of between two consecutive collisions with wall A. Therefore, it will collide times per second with wall A. 

The average change in momentum per molecule per second.  
Therefore, this is the total change in momentum per second for the molecules that collide into wall A. This is the momentum per second that was exerted onto wall A. Because force equals the change in momentum over time, this value is the force exerted on wall A.  
Pressure is defined as force per unit area, so this is the pressure of the gas.  
Because the volume of the container is , we can rearrange the equation.  
The kinetic energy of a single particle is given by this equation.  
Substitute kinetic energy into the equation.  
Substitute the temperature equation (from the previous section).  
Avogadro's number is equal to the number of molecules per mole.  
By definition, the ideal gas constant is equal to the Boltzmann constant times Avogadro's number.  
The ideal gas law is derived from the Kinetic Molecular Theory. 
Deviations from the Ideal Gas LawEdit
In an ideal gas, there are no intermolecular attractions, and the volume of the gas particles is negligible. However, there is no real gas that can perfectly fits this behavior, so the Ideal Gas Law only approximates the behavior of gases. This approximation is very good at high temperatures and low pressures.
At high temperature the molecules have high kinetic energy, so intermolecular attractions are minimized. At low pressure the gas occupies more volume, making the size of the individual molecules negligible. These two factors make the gas behave ideally.
At low temperature or high pressure, the size of the individual molecules and intermolecular attractions becomes significant, and the ideal gas approximation becomes inaccurate.
Eudiometers and Water VaporEdit
Helpful Hint!  

In calculations for a gas above a liquid, the vapor pressure of the liquid must be considered. 
A eudiometer is a device that measures the downward displacement of a gas. The apparatus for this procedure involves an inverted container or jar filled with water and submerged in a water basin. The lid of the jar has an opening for a tube through which the gas to be collected can pass. As the gas enters the inverted container, it forces water to leave the jar (displacing it downward). To fill the entire container with gas, there must enough gas pumped into the container to expel all of the water.
As seen in this diagram, the downward displacement involves water. Therefore, in the container where the gas is collected, there is unwanted water vapor. To account for the water vapor, subtract the pressure of water vapor from the pressure of the gases in the container to find the pressure of the collected gas. This is simply a restatement of Dalton's Law of Partial Pressure:
The pressure of water vapour can be found on this webpage.
Gas Laws Practice QuestionsEdit
 Between the Combined Gas Law and the Ideal Gas Law, which one accounts for chemical change? Explain.
 Calculate the density of hydrogen at a temperature of 298 K and pressure of 100.0 kPa.
 What volume does 5.3 moles of oxygen take up at 313 K and 96.0 kPa?
 Hydrogen and sulfur chemically combine to form the gas hydrogen sulfide, according to the reaction: H_{2 (g)} + S_{(s)} → H_{2}S_{(g)}. How many liters of hydrogen are required to form 7.4 L of hydrogen sulfide (at STP: 273 K, 101.3 kPa)?
Answers to Gas Laws Practice Questions
Avogadro's LawEdit
One mole of gas particles at STP takes up 22.4L
Ideal Gas EquationEdit
PV=nRT, where R = 0.0821 L*atm/K*mol = ideal gas constant. Note how if P is in atm, V is in L, n is in moles, and T is in Kelvin, the units cancel out.
Remember that these gas laws only work in Kelvin.
Graham's LawEdit
For every x times heavier a gas is, it travels times slower:
NonIdeal GasesEdit
When gases are polar, massive, at high pressure and low temperature, they do not behave like ideal gases. They may even condense into liquids or freeze into solids.
The Basics · Periodicity · Solids and Liquids · Gasses · Reactions · Stoichometry · Thermodynamics · Solutions · Acids and Bases · Equilibrium · Electrochemistry · Nuclear Chemistry · Organic Chemistry