AP Chemistry Unit 3.3 Solids, Liquids, and Gas Notes - New Syllabus 2024-2025
AP Chemistry Unit 3.3 Solids, Liquids, and Gas Notes
AP Chemistry Unit 3.3 Solids, Liquids, and Gas Notes – AP Chemistry – per latest AP Chemistry Syllabus.
LEARNING OBJECTIVE
Represent the differences between solid, liquid, and gas phases using a particulate- level model.
Key Concepts:
- The Liquid Phase
- The Gas Phase
3.3.A.1 Types of Solids: Crystalline vs. Amorphous:
1. Crystalline vs. Amorphous Solids:
Property | Crystalline Solids | Amorphous Solids |
---|---|---|
Particle Arrangement | Ordered, repeating pattern | Random arrangement |
Structure | Defined geometric shape, sharp edges | Irregular shape, no sharp edges |
Melting Point | Sharp melting point | Gradual softening over a range |
Anisotropy/Isotropy | Anisotropic (direction-dependent) | Isotropic (direction-independent) |
Examples | Salt (NaCl), metals (Cu, Fe), diamond (C), quartz (SiO₂) | Glass (window glass, silica), rubber, plastics (polyethylene, polystyrene), gelatin |
Hardness/Brittleness | Hard and brittle | Flexible, less brittle |
Optical Properties | Distinct optical properties (e.g., clear, reflective) | Irregular light scattering |
3.3.A.2 Particle Movement and Interactions in Liquids:
1. Particle Arrangement and Movement:
When talking about particle arrangement and movement in solids, liquids, and gases, these three concepts—close packing, freedom of movement, and continuous collisions—are key to understanding the behavior of matter in different states.
i. Close Packing:
In solids, particles (atoms, molecules, or ions) are packed closely together in a regular, repeating pattern, often forming a crystal lattice structure. This close arrangement minimizes the space between particles and contributes to the rigidity and incompressibility of solids. In liquids, particles are still close but can move past one another, so the arrangement is not as ordered as in solids. In gases, the particles are spread out and far apart, with no specific arrangement.
ii. Freedom of Movement:
In solids, the particles vibrate in fixed positions but cannot move freely. This accounts for the rigid structure of solids. In liquids, particles have more freedom—they can slide past each other, allowing liquids to flow and take the shape of their container, though they still retain a definite volume. In gases, particles move freely and rapidly in all directions, leading to the expansion of gases to fill any container and their low density.
iii. Continuous Collisions:
In gases, the particles move rapidly and constantly collide with each other and with the walls of their container. These collisions are elastic, meaning there is no loss of kinetic energy during the process. The frequency and intensity of these collisions contribute to gas pressure. In liquids and solids, the particles still interact with each other, but these interactions are usually less dynamic compared to the fast, random collisions in gases.
These characteristics all come together to define the physical properties of the different states of matter, influencing things like density, shape, and compressibility.
2. Intermolecular Forces:
Intermolecular forces are the attractive forces that act between molecules, and they play a crucial role in determining the physical properties of substances, such as boiling and melting points, solubility, and viscosity. The three types you’ve mentioned—polarity, hydrogen bonding, and van der Waals forces—are all examples of intermolecular forces. Here’s a breakdown:
i. Polarity:
Polarity occurs when there is a distribution of charge within a molecule, resulting in a dipole. This happens when one part of the molecule is slightly positive and another part is slightly negative, due to differences in electronegativity between atoms. Molecules that are polar (like water, H₂O) have regions of partial positive and partial negative charges, which can interact with the opposite charges of other molecules. Polar molecules tend to attract each other, and this attraction can significantly affect the properties of substances. For example, the polarity of water molecules leads to its high surface tension and high boiling point relative to its molecular size.
ii. Hydrogen Bonding:
Hydrogen bonding is a specific, strong type of dipole-dipole interaction that occurs when hydrogen is bonded to highly electronegative elements like fluorine, oxygen, or nitrogen (F, O, N). The hydrogen atom, which carries a partial positive charge, is attracted to the lone pair of electrons on the electronegative atom in a neighboring molecule. This interaction is much stronger than regular dipole-dipole forces and plays a critical role in the behavior of water, the structure of DNA, and protein folding, for example. Hydrogen bonds are responsible for many of water’s unique properties, like its high boiling point, high heat capacity, and ability to dissolve many substances.
iii. Van der Waals Forces (London Dispersion Forces):
These are the weakest of the intermolecular forces and arise due to temporary fluctuations in electron distribution within molecules. Even in nonpolar molecules, the electrons can momentarily create a temporary dipole, which induces a similar dipole in a neighboring molecule. This creates a weak attractive force. While individual van der Waals forces are weak, they can become significant when many molecules are involved (e.g., in larger molecules). Van der Waals forces are responsible for the condensation of nonpolar gases into liquids and for the fact that nonpolar molecules can still interact with each other.
3. Effect of Temperature:
i. Effect on Particle Motion:
a. In Solids:
At lower temperatures, the particles in a solid vibrate slowly around their fixed positions. As the temperature increases, these vibrations become more intense. If the temperature continues to rise and reaches the melting point, the particles gain enough energy to overcome the forces holding them in place, leading to a phase change from solid to liquid.
b. In Liquids:
In liquids, the particles are still close together but can move around each other. As the temperature increases, the particles move faster and have more freedom of motion. This increased kinetic energy can cause the liquid to evaporate if the temperature is high enough to break the intermolecular forces between the particles, turning the liquid into a gas.
c. In Gases:
Gas particles are already moving rapidly in all directions. As temperature increases, the kinetic energy of the gas particles increases as well, making them move even faster. This leads to an increase in pressure if the gas is confined in a container (since faster-moving particles collide with the walls more frequently and with greater force). If the gas is allowed to expand, it will occupy a larger volume due to the higher energy and increased particle motion.
ii. Effect on Kinetic Energy:
a. Kinetic Energy and Temperature:
The kinetic energy of a particle is directly proportional to its temperature. The relationship is given by the equation:
where
is the average kinetic energy,
is the Boltzmann constant, and
is the temperature in Kelvin.
As the temperature increases, the kinetic energy of the particles increases. This increase in kinetic energy leads to faster particle movement and more frequent and energetic collisions, which in turn affects the properties of the substance.
b. Phase Changes and Kinetic Energy:
When a substance undergoes a phase change (e.g., from solid to liquid or liquid to gas), the temperature typically remains constant during the process. During this time, the energy being added or removed is used to overcome intermolecular forces rather than increase kinetic energy. However, once the phase change is complete, any further increase in temperature results in an increase in the kinetic energy of the particles.
iii. General Implications:
a. Increased Temperature:
Higher temperatures generally cause more energetic and faster-moving particles. This can lead to changes in state (e.g., melting or boiling) and can affect properties like viscosity, solubility, and reaction rates.
b. Decreased Temperature:
Lower temperatures reduce the kinetic energy of the particles, leading to slower movement and possibly causing substances to condense or freeze as the particles have less energy to overcome the forces of attraction between them.
3.3.A.3 Similar Molar Volume in Solid and Liquid Phases:
1. Particle Arrangement and Intermolecular Forces:
When considering particle arrangement and intermolecular forces in different phases, both the arrangement of particles and the strength of intermolecular forces can vary significantly between solids and liquids, even though both phases can feature close packing of particles and strong intermolecular forces.
i. Solids: Close Packing and Strong Intermolecular Forces:
a. Particle Arrangement:
In solids, particles are closely packed in a regular, repeating pattern, often forming a crystal lattice structure (in crystalline solids). This close arrangement minimizes the distance between particles, which contributes to the solidity and incompressibility of the material. In amorphous solids (like glass), the particles are still closely packed, but there is no long-range order.
b. Intermolecular Forces:
Solids have strong intermolecular forces (such as ionic, covalent, or metallic bonds, depending on the material). These strong forces hold the particles in place and prevent them from moving freely. The strength of these forces is what gives solids their rigidity and high melting points. For example, metals have metallic bonds, where electrons are shared in a “sea of electrons,” while ionic compounds like sodium chloride (NaCl) are held together by strong electrostatic forces between positively and negatively charged ions.
ii. Liquids: Close Packing and Strong Intermolecular Forces:
a. Particle Arrangement:
In liquids, particles are still close together, but unlike solids, they are not in a fixed position. Instead, they can move around each other (sliding past one another), which allows liquids to flow and take the shape of their container. This arrangement is less ordered than in solids, but the particles are still relatively close compared to gases.
b. Intermolecular Forces:
Liquids also have strong intermolecular forces, which prevent the particles from moving too far apart. For example, in water, hydrogen bonding is the dominant intermolecular force, contributing to its high boiling point, surface tension, and other unique properties. In other liquids, van der Waals forces or dipole-dipole interactions may play a more prominent role. These strong forces in liquids give them definite volumes (unlike gases, which expand to fill any container), but they can still flow.
iii. Comparison:
Close Packing:
Both solids and liquids exhibit close packing of particles, but in solids, the particles are fixed in place, whereas in liquids, the particles can move past one another while still being in close proximity.Strong Intermolecular Forces:
Both phases have strong intermolecular forces. In solids, these forces keep the particles locked in place, giving the substance its rigidity. In liquids, the strong intermolecular forces allow the substance to retain a defined volume while still being able to flow.
2. Molar Volume:
Molar volume refers to the volume occupied by one mole of a substance, typically measured in liters per mole (L/mol). When we discuss similar molar volume in both solids and liquids, we’re focusing on how the particle proximity in both phases results in relatively comparable volumes, despite the different states of matter. Here’s a more detailed breakdown of this concept:
i. Similar Molar Volume in Solids and Liquids:
a. Particle Proximity:
Both in solids and liquids, the particles (atoms, molecules, or ions) are closely packed. In solids, the particles are arranged in a fixed, ordered pattern, while in liquids, the particles are close together but can move past each other. Because the particles are so close in both phases, the volume occupied by one mole of a substance doesn’t change drastically between solid and liquid phases. This is in contrast to gases, where particles are far apart and the molar volume can vary widely with temperature and pressure.
b. Relatively Small Change in Volume:
The change in volume between the solid and liquid phases is typically smaller than the change between the liquid and gas phases. For example, water in its solid form (ice) and liquid form (liquid water) have molar volumes that are quite similar, even though the arrangement and movement of the particles differ between the two phases. Water is a good example of a substance where the molar volume in the solid phase (ice) is slightly larger than in the liquid phase, due to the open, structured arrangement of water molecules in the ice lattice. However, the overall difference in molar volume between the two is relatively small compared to the difference between liquid and gas.
ii. Factors Affecting Molar Volume in Both Phases:
a. Intermolecular Forces:
In both solids and liquids, the particles experience significant intermolecular forces, such as hydrogen bonding in water, which keep them in close proximity. These forces contribute to the similar molar volumes because the particles in both phases are not as far apart as they are in gases.
b. Compression Resistance:
Both solids and liquids are relatively incompressible, meaning that changes in pressure or temperature have less effect on their volume compared to gases. While liquids are generally slightly more compressible than solids, the effect is still much less than in gases.
iii. Why Molar Volumes Differ in Solids and Liquids:
While molar volumes are similar, they can differ slightly due to the different packing arrangements:
- In solids, the particles are typically tightly packed in a regular arrangement, often forming a crystalline structure.
- In liquids, the particles are still relatively close together but lack the rigid structure of solids, allowing for some additional freedom of movement.
The density of a substance is related to its molar volume. Since solids are generally denser than liquids (due to tighter packing), the molar volume of a solid will be slightly smaller than that of the liquid phase.
3.3.A.4 Behavior of Gas Particles and Its Effect on Volume and Shape:
1. Particle Motion and Collisions:
Property | Solids | Liquids | Gases |
---|---|---|---|
Particle Motion | Constant vibration around fixed positions | Move past each other (sliding motion) | Rapid, random motion in all directions |
Collision Frequency | Low (limited to vibrations) | Moderate (frequent collisions) | High (frequent elastic collisions) |
Spacing Between Particles | Very close together (tight packing) | Close, but more space for movement | Far apart (large spacing) |
2. Effect of Temperature, Pressure, and Volume:
The properties of gases are strongly influenced by temperature, pressure, and volume. These factors are described using gas laws. Here’s how each factor influences gas properties:
i. Effect of Temperature on Gas Properties:
a. Temperature affects the kinetic energy of gas particles. As temperature increases, particles move faster, which increases pressure if the volume is constant.
b. At constant volume:
When temperature increases, the kinetic energy of gas molecules rises, leading to more frequent and forceful collisions with container walls, increasing pressure. This relationship is described by Gay-Lussac’s Law:
\[ \frac{P_1}{T_1} = \frac{P_2}{T_2} \]
where:
- \(P\): Pressure
- \(T\): Temperature (in Kelvin)
c. At constant pressure:
When temperature increases, the gas volume expands, described by Charles’s Law:
\[ \frac{V_1}{T_1} = \frac{V_2}{T_2} \]
ii. Effect of Pressure on Gas Properties:
a. Pressure results from gas particles colliding with container walls. Increasing pressure compresses gas, reducing volume (constant temperature).
b. At constant temperature:
Boyle’s Law states:
\[ P_1 V_1 = P_2 V_2 \]
iii. Effect of Volume on Gas Properties:
a. Volume determines the space for gas particles. Reducing volume at constant temperature increases pressure.
b. At constant pressure:
Increasing the volume at constant pressure increases the space available for gas particles, leading to potential temperature changes.
iv. Combined Gas Law:
The Combined Gas Law relates temperature, pressure, and volume:
\[ \frac{P_1 V_1}{T_1} = \frac{P_2 V_2}{T_2} \]
- \(P\): Pressure
- \(V\): Volume
- \(T\): Temperature (in Kelvin)
The Three States of Matter
- Gas: molecules/atoms have enough energy to move freely
- Particles so far apart from each other that intermolecular forces not considered
- Indefinite shape and volume
- Liquid: strong intermolecular forces and molecular motions
- Particles are always in contact but have enough energy to slide past each other
- Indefinite shape & definite volume
- Solid: strongest intermolecular forces, but the molecular motions are minimal
- Particles don’t have enough energy to move → always in contact and in fixed position
- Definite shape and definite volume
Characteristics
- Particles retain their chemical identity in all 3 states, but the volume, density, and interparticle distances are different
- Liquids & solids are incompressible (condensed state) & their density does not change with temperature
- These similarities are due to the molecules being close together in solids and liquids; far apart in gases
The Liquid State
- Liquids have low compressibility, lack of rigidity, and high density compared to gasses
- Surface tension: tendency of molecules to be pulled from the surface to the interior of a liquid; resistance of a liquid to an increase in its surface area
- Stronger InterMF = stronger surface tension b/c molecules resist being stretched/broken
- Viscosity: a measure of a liquid’s resistance to flow
- Capillary action: spontaneous rising of a liquid in a narrow tube
- Capillary action depends on the cohesive and adhesive forces present → during capillary action, the liquid molecules simultaneously adhere to the tubing while pulling each other up
- Cohesive forces: intermolecular forces among the molecules of the liquid
- Molecules attracted to same molecules
- Adhesive forces: forces between the liquid molecules and their container
- Molecules attracted to another type of molecule
- Cohesive forces: intermolecular forces among the molecules of the liquid
- Capillary action depends on the cohesive and adhesive forces present → during capillary action, the liquid molecules simultaneously adhere to the tubing while pulling each other up
Concave Meniscus Formed by Polar Water
- Water has both strong adhesive and cohesive forces, but bcuz the adhesive forces are stronger → water will have a concave meniscus (water is attracted to the glass)
- Nonpolar liquids have stronger cohesive than adhesive forces (not attracted to glass) → convex meniscus
Changes of State
- Phase Changes: when a substance changes from solid to liquid to gas
Changes of State | Melting or Fusion |
Solid → Liquid | Melting (endo) |
Liquid → Solid | Freezing (exo) |
Liquid → Gas | Vaporization (endo) |
Gas → Liquid | Condensation (exo) |
Gas → Solid | Deposition (exo) |
Solid → Gas | Sublimation (endo) |
- Melting point: temp at which the substance goes from a solid to a liquid (or from a liquid to a solid)
- The strength of the InterMF determines the temp at which these phase changes will occur
- Boiling point: temp at which a substance goes from a liquid to a gas (or from a gas to a liquid)
- 2 Key Points
- At a substance’s MP or BP, two phases can exist simultaneously
- The temp of a substance does not change as the substance goes from one phase to another
- Only after all of the substance has changed phases does adding heat change the temp of the substance
- Heat of fusion:ΔHfus·: The enthalpy change that occurs at the melting point when a solid melts
- When curve quickly changes slope to 0, all energy is used to overcome intermolecular forces holding the substance’s molecules together
Evaporation
- Evaporation: liquid becomes gas below a substances BP (occurs only for particles at the surface of a liquid)
- The particles with the highest KE can overcome the InterMF forces within the liquid and evaporate as gas
- Is a cooling process because the particles with the highest KE diffuse away from the liquid so the average KE of remaining particles decrease
Boiling
- Boiling: process by which a liquid becomes a vapor when it is heated to its boiling point
- As temp of liquid increases, vapor pressure increases until the vapor pressure of the liquid become equal to the surrounding atmospheric pressure → At this temp the liquid will boil (BP)
- As atmospheric pressure increase, BP of liquid increases
- The normal BP is the temperature at which the liquid boils at standard pressure
Evaporation vs Boiling
- Vaporization occurs in two ways: boiling and evaporation
- Evaporation is slower, occurs only from the surface of the liquid, does not produce bubbles, and leads to cooling.
- Boiling is faster, can occur throughout the liquid, produces lots of bubbles, and does not result in cooling.
Vapor Pressure and Changes of State
- Vapor Pressure: Liquid molecules at the surface escape into the gas phase → gas particles create pressure above the liquid in a closed container
- Gases are often collected over water so the vapor pressure of water must be subtracted from the total pressure in calculations
- Weaker IMF → Lower BP → will have higher vapor pressure before reaching boiling point
- Liquids are said to be volatile—they evaporate rapidly from an open dish
- Stronger IMF → higher BP/fewer molecules break away → will have lower vapor pressure before reaching boiling point.
- Heat of vaporization ΔHvap•:The energy required to vaporize 1 mole of a liquid at a pressure of 1 atm
- Water has high HoV so can absorb lots of heat and resist chemical change; needs lots of energy to freeze → cools air when it is warm and releases heat in the winter, stabilizes ocean temperature, climate
- Generally, the vapor pressure of a liquid is related to temperature and intermolecular forces
- Vapor pressure increases significantly with temperature.
- Temperature of the liquid increases = more molecules will have the minimum energy needed to overcome InterMF and escape into the vapor phase
- Vapor pressure increases significantly with temperature.
Phase Diagrams
- Phase diagram: way of representing the phases of a substance as a function of temperature and pressure. (in a closed system)
- Lines represent phase changes
- Triple point: condition of temp and pressure where all three phases are present
- Critical temperature: temperature above which the vapor cannot be liquefied no matter what pressure is applied
- Critical pressure: pressure required to produce liquefaction at the critical temperature
- Critical point: critical temperature + critical pressure
Phase Diagram for Water
- Density and Phase Diagrams: the slope of the line between the solid and liquid region indicates which of these 2 phases is denser 1
- MP Curve has positive slope (/) → solid is denser
- Increasing pressure = increases melting point
- MP curve has negative slope (\)→ liquid is denser
- Increasing pressure = decreases melting point
- Water has a negative slope, but most other substances have a positive slope
- Increasing pressure = decreases melting point