Introduction: Understanding Gas Behavior
Gas laws are fundamental principles that describe how gases behave under different conditions of temperature, pressure, and volume. These relationships form the cornerstone of numerous scientific and engineering applications, from weather forecasting to medical respiratory therapy. This comprehensive cheat sheet covers the major gas laws, their mathematical formulations, practical applications, and problem-solving strategies, serving as both a quick reference and a study aid for students, educators, and professionals working with gaseous systems.
Fundamental Gas Properties
Key Gas Variables
| Variable | Symbol | SI Unit | Other Common Units | Description |
|---|---|---|---|---|
| Pressure | P | Pascal (Pa) | atm, mmHg, torr, bar, psi | Force per unit area exerted by gas molecules |
| Volume | V | Cubic meter (m³) | L, mL, cm³ | Space occupied by the gas |
| Temperature | T | Kelvin (K) | °C, °F | Measure of average kinetic energy of molecules |
| Amount of Gas | n | Mole (mol) | g, kg | Quantity of gas particles |
| Universal Gas Constant | R | 8.314 J/(mol·K) | 0.08206 L·atm/(mol·K) | Proportionality constant in gas laws |
Common Pressure Unit Conversions
| From | To | Conversion Factor |
|---|---|---|
| atm | Pa | 1 atm = 101,325 Pa |
| atm | mmHg (torr) | 1 atm = 760 mmHg |
| atm | bar | 1 atm = 1.01325 bar |
| atm | psi | 1 atm = 14.7 psi |
| Pa | atm | 1 Pa = 9.87 × 10⁻⁶ atm |
| mmHg | atm | 1 mmHg = 1.32 × 10⁻³ atm |
| bar | atm | 1 bar = 0.987 atm |
| kPa | atm | 1 kPa = 9.87 × 10⁻³ atm |
Temperature Conversions
| Conversion | Formula |
|---|---|
| Celsius to Kelvin | K = °C + 273.15 |
| Kelvin to Celsius | °C = K – 273.15 |
| Fahrenheit to Celsius | °C = (°F – 32) × 5/9 |
| Celsius to Fahrenheit | °F = (°C × 9/5) + 32 |
| Fahrenheit to Kelvin | K = (°F – 32) × 5/9 + 273.15 |
Individual Gas Laws
Boyle’s Law
Statement: At constant temperature, the volume of a fixed amount of gas is inversely proportional to its pressure.
Mathematical Form: P₁V₁ = P₂V₂ (when T and n are constant)
Graphical Representation:
- P vs. V: Hyperbola
- P vs. 1/V: Straight line with positive slope
- PV vs. P: Horizontal line
Key Concepts:
- As pressure increases, volume decreases proportionally
- Doubling the pressure halves the volume
- The product PV remains constant
Example Problem: A gas occupies 2.5 L at 1.0 atm. What volume will it occupy at 2.5 atm if temperature remains constant?
Solution:
- Given: P₁ = 1.0 atm, V₁ = 2.5 L, P₂ = 2.5 atm
- Using Boyle’s Law: P₁V₁ = P₂V₂
- V₂ = (P₁V₁)/P₂ = (1.0 atm × 2.5 L)/2.5 atm = 1.0 L
Charles’s Law
Statement: At constant pressure, the volume of a fixed amount of gas is directly proportional to its absolute temperature.
Mathematical Form: V₁/T₁ = V₂/T₂ (when P and n are constant)
Graphical Representation:
- V vs. T: Straight line with positive slope
- V vs. 1/T: Hyperbola
- V/T vs. T: Horizontal line
Key Concepts:
- As temperature increases, volume increases proportionally
- Doubling the absolute temperature doubles the volume
- The ratio V/T remains constant
- Volume would theoretically be zero at absolute zero (-273.15°C or 0 K)
Example Problem: A gas has a volume of 500 mL at 25°C. What will its volume be at 100°C if pressure remains constant?
Solution:
- Given: V₁ = 500 mL, T₁ = 25°C = 298.15 K, T₂ = 100°C = 373.15 K
- Using Charles’s Law: V₁/T₁ = V₂/T₂
- V₂ = V₁(T₂/T₁) = 500 mL × (373.15 K/298.15 K) = 626 mL
Gay-Lussac’s Law
Statement: At constant volume, the pressure of a fixed amount of gas is directly proportional to its absolute temperature.
Mathematical Form: P₁/T₁ = P₂/T₂ (when V and n are constant)
Graphical Representation:
- P vs. T: Straight line with positive slope
- P vs. 1/T: Hyperbola
- P/T vs. T: Horizontal line
Key Concepts:
- As temperature increases, pressure increases proportionally
- Doubling the absolute temperature doubles the pressure
- The ratio P/T remains constant
- Pressure would theoretically be zero at absolute zero
Example Problem: A gas exerts a pressure of 1.5 atm at 30°C. What pressure will it exert at 80°C if volume remains constant?
Solution:
- Given: P₁ = 1.5 atm, T₁ = 30°C = 303.15 K, T₂ = 80°C = 353.15 K
- Using Gay-Lussac’s Law: P₁/T₁ = P₂/T₂
- P₂ = P₁(T₂/T₁) = 1.5 atm × (353.15 K/303.15 K) = 1.75 atm
Avogadro’s Law
Statement: At constant temperature and pressure, the volume of a gas is directly proportional to the number of moles of the gas.
Mathematical Form: V₁/n₁ = V₂/n₂ (when P and T are constant)
Key Concepts:
- As the amount of gas increases, volume increases proportionally
- Doubling the number of moles doubles the volume
- The ratio V/n remains constant
Example Problem: 2.0 moles of an ideal gas occupy 44.8 L at STP. What volume will 5.0 moles occupy under the same conditions?
Solution:
- Given: n₁ = 2.0 mol, V₁ = 44.8 L, n₂ = 5.0 mol
- Using Avogadro’s Law: V₁/n₁ = V₂/n₂
- V₂ = V₁(n₂/n₁) = 44.8 L × (5.0 mol/2.0 mol) = 112 L
Combined Gas Law
Statement: Combines Boyle’s, Charles’s, and Gay-Lussac’s laws into a single expression.
Mathematical Form: P₁V₁/T₁ = P₂V₂/T₂ (when n is constant)
Key Concepts:
- Allows calculation of unknown gas properties when amount of gas is constant
- Simplifies to individual gas laws when appropriate variables are held constant
- The ratio PV/T remains constant
Example Problem: A gas has a volume of 3.0 L at 2.0 atm and 27°C. What will its volume be at 1.0 atm and 127°C?
Solution:
- Given: P₁ = 2.0 atm, V₁ = 3.0 L, T₁ = 27°C = 300 K, P₂ = 1.0 atm, T₂ = 127°C = 400 K
- Using the Combined Gas Law: P₁V₁/T₁ = P₂V₂/T₂
- V₂ = V₁(P₁/P₂)(T₂/T₁) = 3.0 L × (2.0 atm/1.0 atm) × (400 K/300 K) = 8.0 L
Ideal Gas Law
Fundamental Equation and Variations
Ideal Gas Law Equation: PV = nRT
Where:
- P = pressure
- V = volume
- n = number of moles
- R = universal gas constant
- T = absolute temperature (Kelvin)
Universal Gas Constant (R) Values in Different Units:
| Units | R Value |
|---|---|
| J/(mol·K) | 8.314 |
| L·atm/(mol·K) | 0.08206 |
| L·torr/(mol·K) | 62.36 |
| cal/(mol·K) | 1.987 |
| m³·Pa/(mol·K) | 8.314 |
Variations of the Ideal Gas Law:
| Variation | Equation | Use |
|---|---|---|
| Density Form | P = ρRT/M | Relates pressure to gas density (ρ) and molar mass (M) |
| Number of Molecules Form | PV = NkT | Uses number of molecules (N) and Boltzmann constant (k) |
| Molar Volume | Vm = RT/P | Volume of one mole of gas at given conditions |
Standard Conditions
| Standard | Temperature | Pressure | Molar Volume |
|---|---|---|---|
| STP (Standard Temperature and Pressure, IUPAC) | 0°C (273.15 K) | 1 bar (100 kPa) | 22.71 L/mol |
| Old STP | 0°C (273.15 K) | 1 atm (101.325 kPa) | 22.41 L/mol |
| SATP (Standard Ambient Temperature and Pressure) | 25°C (298.15 K) | 1 atm (101.325 kPa) | 24.47 L/mol |
| NTP (Normal Temperature and Pressure) | 20°C (293.15 K) | 1 atm (101.325 kPa) | 24.04 L/mol |
Key Calculations Using the Ideal Gas Law
Finding Moles: n = PV/RT
Finding Volume: V = nRT/P
Finding Pressure: P = nRT/V
Finding Temperature: T = PV/nR
Example Problem 1: Calculate the number of moles in 2.5 L of gas at 1.5 atm and 25°C.
Solution:
- Given: V = 2.5 L, P = 1.5 atm, T = 25°C = 298.15 K, R = 0.08206 L·atm/(mol·K)
- Using n = PV/RT: n = (1.5 atm × 2.5 L)/(0.08206 L·atm/(mol·K) × 298.15 K) = 0.153 mol
Example Problem 2: A gas sample contains 0.25 mol and exerts a pressure of 2.0 atm at 20°C. What is its volume?
Solution:
- Given: n = 0.25 mol, P = 2.0 atm, T = 20°C = 293.15 K, R = 0.08206 L·atm/(mol·K)
- Using V = nRT/P: V = (0.25 mol × 0.08206 L·atm/(mol·K) × 293.15 K)/2.0 atm = 3.01 L
Gas Mixtures
Dalton’s Law of Partial Pressures
Statement: The total pressure of a gas mixture equals the sum of the partial pressures of each component.
Mathematical Form: Ptotal = P₁ + P₂ + P₃ + … + Pₙ
Partial Pressure: Pᵢ = xᵢ × Ptotal, where xᵢ is the mole fraction of gas i
Mole Fraction: xᵢ = nᵢ/ntotal, where nᵢ is the number of moles of gas i
Key Concepts:
- Each gas in a mixture behaves independently
- Partial pressure is the pressure that each gas would exert if it occupied the container alone
- Mole fractions sum to 1: x₁ + x₂ + … + xₙ = 1
Example Problem: A gas mixture contains 2.0 mol O₂, 5.0 mol N₂, and 3.0 mol CO₂. If the total pressure is 5.0 atm, what is the partial pressure of each gas?
Solution:
- Calculate total moles: ntotal = 2.0 + 5.0 + 3.0 = 10.0 mol
- Calculate mole fractions:
- xO₂ = 2.0/10.0 = 0.20
- xN₂ = 5.0/10.0 = 0.50
- xCO₂ = 3.0/10.0 = 0.30
- Calculate partial pressures:
- PO₂ = 0.20 × 5.0 atm = 1.0 atm
- PN₂ = 0.50 × 5.0 atm = 2.5 atm
- PCO₂ = 0.30 × 5.0 atm = 1.5 atm
- Verify: 1.0 + 2.5 + 1.5 = 5.0 atm ✓
Graham’s Law of Diffusion and Effusion
Statement: The rate of diffusion or effusion of a gas is inversely proportional to the square root of its molar mass.
Mathematical Form: Rate₁/Rate₂ = √(M₂/M₁)
Key Concepts:
- Lighter gases diffuse and effuse faster than heavier gases
- The ratio of diffusion rates equals the inverse ratio of the square roots of their molar masses
- Applies to both diffusion (movement through another gas) and effusion (movement through a tiny hole)
Example Problem: Hydrogen gas (H₂) effuses through a porous barrier 4.0 times faster than an unknown gas. What is the molar mass of the unknown gas?
Solution:
- Given: RateH₂/RateX = 4.0, MH₂ = 2.0 g/mol
- Using Graham’s Law: RateH₂/RateX = √(MX/MH₂)
- 4.0 = √(MX/2.0 g/mol)
- Square both sides: 16.0 = MX/2.0 g/mol
- MX = 16.0 × 2.0 g/mol = 32.0 g/mol (possibly O₂)
Kinetic Molecular Theory of Gases
Key Postulates
- Gases consist of tiny particles (molecules or atoms) in constant, random motion
- Gas particles are separated by large distances; actual volume of particles is negligible
- Gas particles have negligible intermolecular forces
- Collisions between particles and with container walls are perfectly elastic
- Average kinetic energy of gas particles is directly proportional to absolute temperature
Important Equations
| Equation | Description |
|---|---|
| Average Kinetic Energy | Eavg = (3/2)kT = (3/2)(R/NA)T |
| Root Mean Square Velocity | vrms = √(3RT/M) |
| Most Probable Velocity | vmp = √(2RT/M) |
| Average Velocity | vavg = √(8RT/πM) |
Where:
- k = Boltzmann constant (1.38 × 10⁻²³ J/K)
- T = absolute temperature (K)
- R = gas constant (8.314 J/(mol·K))
- NA = Avogadro’s number (6.022 × 10²³ particles/mol)
- M = molar mass (kg/mol)
Example Problem: Calculate the root mean square velocity of nitrogen molecules (N₂) at 25°C.
Solution:
- Given: T = 25°C = 298.15 K, M(N₂) = 28.0 g/mol = 0.0280 kg/mol
- Using vrms = √(3RT/M): vrms = √(3 × 8.314 J/(mol·K) × 298.15 K/0.0280 kg/mol) vrms = √(265,553 J/kg) = √(265,553 m²/s²) = 515 m/s
Non-Ideal Gas Behavior
Van der Waals Equation
Equation: (P + a(n/V)²)(V – nb) = nRT
Where:
- a accounts for attractive forces between molecules
- b accounts for the volume occupied by gas molecules themselves
Compressibility Factor: Z = PV/nRT
- Z = 1 for ideal gases
- Z < 1 indicates attractive forces dominate
- Z > 1 indicates repulsive forces dominate
Conditions When Gases Behave Non-Ideally
| Condition | Effect on Ideal Behavior |
|---|---|
| High Pressure | Increases molecular interactions and effective volume |
| Low Temperature | Decreases molecular kinetic energy, increasing effect of attractive forces |
| Complex Molecules | Increase intermolecular forces and effective molecular volume |
Example Problem: Calculate the pressure of 1.00 mol of CO₂ in a 1.00 L container at 300 K using: a) Ideal gas law b) Van der Waals equation (For CO₂: a = 3.64 L²·atm/mol² and b = 0.0427 L/mol)
Solution: a) Using ideal gas law: P = nRT/V = (1.00 mol × 0.08206 L·atm/(mol·K) × 300 K)/1.00 L = 24.6 atm
b) Using Van der Waals equation: P = nRT/(V – nb) – a(n/V)² P = (1.00 mol × 0.08206 L·atm/(mol·K) × 300 K)/(1.00 L – 1.00 mol × 0.0427 L/mol) – 3.64 L²·atm/mol² × (1.00 mol/1.00 L)² P = 24.6 atm/(0.9573) – 3.64 atm = 25.7 atm – 3.64 atm = 22.1 atm
Problem-Solving Strategies
1. General Problem-Solving Approach
Identify the known and unknown variables
- Write down all given information
- Convert all units to a consistent system (preferably SI)
- Identify what you need to find
Select the appropriate gas law
- Determine which variables are changing and which remain constant
- Choose the law that relates the variables you have with the ones you need
Set up the equation and solve
- Substitute the known values
- Rearrange to isolate the unknown variable
- Calculate and double-check your work
Verify your answer
- Check that units are correct
- Ensure the answer makes physical sense
- Confirm magnitude with estimation
2. Typical Problem Types
| Problem Type | Approach |
|---|---|
| Fixed Amount of Gas (changing P, V, T) | Use combined gas law: P₁V₁/T₁ = P₂V₂/T₂ |
| Unknown Amount of Gas | Use ideal gas law: PV = nRT |
| Gas Mixtures | Use Dalton’s law and partial pressures |
| Gas Collection Over Water | Subtract water vapor pressure from total pressure to find dry gas pressure |
| Gas Density | Use ρ = PM/RT or ρ = nM/V |
| Reaction Stoichiometry with Gases | Determine moles using ideal gas law, then apply stoichiometry |
3. Common Conversion Factors and Relationships
| Conversion | Relationship |
|---|---|
| Volume of 1 mol at STP | 22.4 L (approx.) |
| Density of gas to molar mass | M = ρRT/P |
| Gas constant conversion | R = 8.314 J/(mol·K) = 0.08206 L·atm/(mol·K) |
| Mole to mass conversion | m = n × M |
| Mole to molecules conversion | N = n × NA |
Practical Applications of Gas Laws
Laboratory Applications
| Application | Relevant Gas Law | Description |
|---|---|---|
| Gas Collection | Dalton’s Law | Collecting gases over water and accounting for water vapor pressure |
| Measuring Molar Mass | Ideal Gas Law | Using gas density to determine unknown molar mass |
| Gas Chromatography | Graham’s Law | Separation of compounds based on diffusion rates |
| Vacuum Systems | Boyle’s Law | Design and operation of vacuum pumps and systems |
| Gas Storage | Combined Gas Law | Safe storage of compressed gases in cylinders |
Real-World Applications
| Application | Relevant Gas Law | Description |
|---|---|---|
| Weather Balloons | Charles’s Law | Expansion of balloon as it rises to higher altitudes |
| Scuba Diving | Boyle’s Law | Pressure changes affecting breathing gas volume with depth |
| Tire Pressure | Gay-Lussac’s Law | Increase in tire pressure as temperature rises |
| Breathing Physiology | Dalton’s Law | Partial pressures of gases in respiratory system |
| Aerosol Cans | Vapor Pressure | Propellant behavior in pressurized containers |
| Hot Air Balloons | Charles’s Law | Decreased density of hot air causing balloon to rise |
| Automobile Engines | Combined Gas Law | Compression and expansion in combustion cycle |
Common Mistakes and How to Avoid Them
| Common Mistake | Prevention Strategy |
|---|---|
| Forgetting to convert to Kelvin | Always check temperature units and convert to Kelvin before using in gas laws |
| Using incorrect units for R | Match units of R with the units of your other variables |
| Assuming standard conditions | Verify specific conditions (T, P) for each problem |
| Misidentifying constant variables | Clearly identify which variables change and which remain constant |
| Incorrect mole calculations | Double-check stoichiometry and unit conversions |
| Neglecting water vapor pressure | When collecting gases over water, remember to subtract water vapor pressure |
| Applying ideal gas law under extreme conditions | Consider using van der Waals equation for high P or low T |
This cheat sheet provides a comprehensive overview of gas laws and their applications. Remember that while these laws accurately describe gas behavior under many conditions, real gases may deviate from ideal behavior, particularly at high pressures and low temperatures. Always consider the specific conditions of your system when applying these principles.
