CHEM 11_Chapter 11 - Properties of Gases
11.1 Gases: Properties and Behavior
Key Terms
Kinetic Molecular Theory of Gases:
Scientific model explaining the behavior of gases.
Based on assumptions about particle motion, energy, and interactions.
Ideal Gas:
Hypothetical gas defined by specific characteristics:
High translational kinetic energy.
No attractive or repulsive forces between particles.
Collisions are elastic, conserving total kinetic energy.
Particle volume is negligible compared to the container's volume.
Average kinetic energy is directly related to temperature.
States of Matter and Particle Behavior
Solids:
Constant shape and volume, almost incompressible.
Particles:
Arranged in a fixed, regular pattern.
Vibrate in place but do not move past each other.
Liquids:
Variable shape, constant volume, almost incompressible.
Particles:
Less organized, able to slide past each other.
Allow liquids to flow and take the shape of their container.
Gases:
Variable shape and volume, compressible.
Particles:
Highly disorganized, widely separated, move freely in all directions.
Bounce off each other and the container walls.
Changes of State
Determined by two factors:
Attractive Forces: Hold particles together.
Stronger forces require more kinetic energy to overcome.
Kinetic Energy: Tends to pull particles apart.
Attractive Forces That Influence the State of Matter
Stronger:
Attractions between oppositely charged particles (IONS)
State: Solid
Example: Table salt (NaCl(s))
Attractions between polar molecules
State: Solid, liquid, gas
Examples:
Glucose (C6H12O6(s))
Ethanol (CH3CH2OH())
Ammonia (NH3(g))
Weaker:
Attractions between non-polar molecules
State: Solid, liquid, gas
Examples:
Paraffin (C30H62(s))
Pentane (C5H12())
Carbon dioxide (CO2(g))
Attractive Forces Between Particles
Attractive Forces Between Oppositely Charged Particles:
Electrostatic attractions: Oppositely charged particles pull towards each other (like magnets).
Example: Ionic compounds have very strong bonds due to these attractions. A positive ion is attracted to the negative ion.
Result: Ionic compounds, like NaCl, are solid at room temperature.
Attractive Forces Between Polar Molecules:
Polar molecules have partial positive and partial negative ends, creating a permanent dipole-dipole effect.
Dipole bonds between polar molecules are weaker than ionic bonds.
Result: Substances with polar molecules often remain as liquids or gases at room temperature.
Hydrogen Bonds:
A type of dipole-dipole interaction.
Strength depends on the type of bond:
O–H bonds are stronger than N–H bonds.
Example: Water (liquid at room temperature) has stronger O–H hydrogen bonds than ammonia (gas at room temperature).
Attractive Forces Between Non-Polar Molecules:
Forces arise from temporary dipoles.
Large non-polar molecules tend to be liquids at room temperature because their size increases attractive forces.
Key Relationships:
Larger molecules = Stronger attractive forces.
Stronger forces = More energy (heat) needed to cause a state change.
Kinetic Energy and Motion of Particles
Three types of particle motion:
Vibrational Motion: Back-and-forth movement (all states).
Rotational Motion: Spinning on an axis (liquids, gases, some solids).
Translational Motion: Movement from one place to another (liquids, gases).
Temperature:
Directly related to the average kinetic energy of particles.
Heating increases particle motion (vibrational, rotational, and translational).
Higher temperatures allow particles to overcome attractive forces, leading to state changes.
Distinguishing Properties of Gases
Compressibility:
Gases can be compressed significantly due to large spaces between particles.
Solids and liquids are nearly incompressible.
Thermal Expansion:
Gases expand greatly with temperature increase (at constant pressure).
Solids and liquids expand minimally.
Low Viscosity:
Gases flow freely due to minimal intermolecular forces.
Low Density:
Gas densities are much lower than those of solids and liquids.
Miscibility:
Gases mix completely with other gases due to negligible particle volume and high mobility.
The Kinetic Molecular Theory of Gases
Constant Random Motion:
Particles travel in straight lines until collisions occur.
Negligible Volume:
Individual gas particles are considered point masses with negligible size.
No Interparticle Forces:
No attractions or repulsions between particles.
Elastic Collisions:
Total kinetic energy is conserved during collisions.
Temperature-Kinetic Energy Relationship:
Average kinetic energy increases with temperature.
Behavior of Real Gases vs. Ideal Gases
Ideal Gas Behavior: Accurate under ordinary temperatures and pressures.
Deviations: Occur at very high pressures or low temperatures where particle volume and intermolecular forces cannot be ignored.
11.2 Gases and Pressure Changes
Key Terms
Viscosity:
Resistance of a liquid to flow.
Influenced by temperature and intermolecular forces.
Example: Honey has higher viscosity than water.
Surface Tension:
The energy required to increase a liquid’s surface area.
Results from cohesive forces between molecules.
Example: Water droplets form spheres due to high surface tension.
Capillary Action:
The ability of a liquid to flow against gravity in a narrow tube.
Caused by the combination of adhesive forces (to the tube) and cohesive forces (within the liquid).
Example: Water rising in a thin straw.
Distinguishing Properties of Liquids
Definite Volume, Indefinite Shape:
Liquids retain volume but take the shape of their container.
Incompressibility:
Liquids resist compression due to closely packed particles.
Fluidity:
Liquids flow due to their ability to slide past one another.
Lower viscosity = higher fluidity.
Density:
Liquids are denser than gases but less dense than solids (in most cases).
Intermolecular Forces in Liquids
Dipole-Dipole Interactions:
Found in polar molecules.
Moderate strength.
Example: Hydrogen bonds in water.
London Dispersion Forces:
Present in all molecules, strongest in large, non-polar molecules.
Example: Dispersion forces in bromine (Br2).
Hydrogen Bonding:
A special type of dipole interaction involving H bonded to N, O, or F.
Example: Water (H2O) has strong hydrogen bonds.
Factors Affecting Liquid Properties
Temperature:
Higher temperatures reduce viscosity and surface tension.
Example: Heating honey makes it flow more easily.
Intermolecular Forces:
Stronger forces lead to higher viscosity and surface tension.
Example: Water’s high surface tension due to hydrogen bonding.
Particle Size and Shape:
Larger or irregularly shaped particles increase viscosity.
Capillary Action Explained
Adhesive Forces:
Attraction between liquid molecules and a solid surface.
Stronger adhesive forces cause liquids to "climb" surfaces.
Cohesive Forces:
Attraction between liquid molecules themselves.
Cohesion prevents the liquid from spreading too thin.
Examples:
Water rises in plant roots due to capillary action.
Mercury forms a convex meniscus due to stronger cohesion than adhesion.
Evaporation and Vapour Pressure
Evaporation:
Surface particles with sufficient kinetic energy escape into the gas phase.
Increases with temperature and surface area.
Vapour Pressure:
Pressure exerted by a liquid’s vapor in a closed system.
Higher temperatures = higher vapor pressure.
Boiling Point:
The temperature at which vapor pressure equals external pressure.
Stronger intermolecular forces = higher boiling point.
Dynamic Equilibrium in Liquids
Definition:
When the rate of evaporation equals the rate of condensation in a closed system.
Example:
A sealed bottle of water reaches equilibrium between liquid and vapor phases.
11.3 Gases and Temperature Changes
Charles's Law
Direct Proportionality: Volume of a gas is directly proportional to its Kelvin temperature when pressure and the amount of gas (number of moles) remain constant.
This means that if the temperature of a gas increases, its volume will also increase proportionally, and vice versa, as long as pressure and the amount of gas stay the same.
Mathematical Expression:
V ∝ T (V is directly proportional to T)
V1/T1 = V2/T2 (where V1 and T1 are the initial volume and temperature, and V2 and T2 are the final volume and temperature)
Temperature in Kelvin:
Temperature must always be expressed in Kelvin (K) for Charles's Law to hold true.
K = °C + 273.15
Graph of V vs. T (in Kelvin):
A straight line passing through the origin (0,0) on a graph of volume (V) versus Kelvin temperature (T). This visually represents the direct proportionality.
Kinetic Molecular Theory Explanation:
Increased Temperature:
Leads to increased kinetic energy of the gas molecules.
Molecules move faster and collide more frequently and with greater force.
Constant Pressure:
To maintain constant pressure, the volume of the container must increase to accommodate the increased molecular motion.
This is because the increased collisions exert a greater force on the container walls, and a larger volume reduces the frequency and force of these collisions.
Gay-Lussac's Law
Direct Proportionality: Pressure of a gas is directly proportional to its Kelvin temperature when volume and the amount of gas (number of moles) remain constant.
This means that if the temperature of a gas increases, its pressure will also increase proportionally, and vice versa, as long as volume and the amount of gas stay the same.
Mathematical Expression:
P ∝ T (P is directly proportional to T)
Temperature in Kelvin:
Temperature must always be expressed in Kelvin (K) for Gay-Lussac's Law to hold true.
Kinetic Molecular Theory Explanation:
Increased Temperature:
Leads to increased kinetic energy of the gas molecules.
Molecules move faster and collide more frequently and with greater force.
Constant Volume:
Since the volume of the container cannot change, the increased collisions result in a significant increase in pressure exerted on the container walls.
Key Points for Both Laws
Ideal Gas Behavior: These laws describe the behavior of ideal gases. Real gases may exhibit slight deviations, particularly at high pressures or low temperatures.
Practical Applications: Both Charles's Law and Gay-Lussac's Law have significant practical applications in various fields, including:
Weather forecasting
Aviation
Industrial processes (e.g., manufacturing, chemical engineering)