Bonding, Structure, and Gases
Lattice Structures
- Most ionic, metallic, and covalent compounds form crystalline lattices.
- Ions, atoms, or molecules are arranged in a regular, repeating pattern within these lattices.
Giant Ionic Lattices
- An ionic bond is the electrostatic force of attraction between a positively charged metal ion (cation) and a negatively charged non-metal ion (anion).
- Metals become positively charged by transferring electrons to non-metals, which then become negatively charged.
- Ionic compounds arrange themselves into giant ionic lattices (also called giant ionic structures).
- The specific type of lattice structure depends on the relative sizes of the positive and negative ions, which are arranged in an alternating pattern.
- Examples of ionic lattices with a cubic structure include Magnesium Oxide (MgO) and Sodium Chloride (NaCl).
- In general ionic lattices, negative ions (anions) are typically larger than the positive ions (cations).
- The ionic lattices for NaCl and MgO are similar due to the 1:1 ratio of cations to anions.
Covalent Lattices
- Covalent bonds involve the sharing of electrons between non-metal atoms.
- Covalent compounds can form simple molecular lattices or giant molecular lattices.
- Simple molecular lattices: Examples include iodine (I<em>2), buckminsterfullerene (C</em>60), and ice (H2O).
- Giant molecular lattices: Examples include silicon(IV) oxide (SiO2), graphite, and diamond.
- Different simple molecular lattices (e.g., ice, buckminsterfullerene, iodine) exhibit different structures and intermolecular forces.
- Giant molecular lattices generally have higher melting and boiling points due to the significant energy needed to overcome intramolecular and/or intermolecular forces.
- Metals form giant metallic lattices where metal ions are surrounded by a 'sea' of delocalized electrons.
- Metal ions are often arranged in hexagonal layers or cubic arrangements.
- In copper (Cu), the cations are arranged in regular layers.
Allotropes of Carbon
- Graphite, diamond, and buckminsterfullerene are allotropes of carbon.
- Allotropes are different structural forms of the same element.
Bonding & Structure and Physical Properties
- Different types of bonding and structure influence physical properties like melting and boiling points, electrical conductivity, and solubility.
Ionic Bonding & Giant Ionic Lattice Structures
- Ionic compounds are strong due to strong electrostatic forces that hold the ions together.
- They tend to be brittle because ionic crystals can easily split apart under stress.
- Ionic compounds have high melting and boiling points because strong electrostatic forces between ions act in all directions, maintaining a strong lattice.
- Melting and boiling points increase with the charge density of the ions due to greater electrostatic attraction. For example, Mg2+O2− has a higher melting point than Na+Cl−.
- Ionic compounds are often soluble in water because they can form ion-dipole bonds.
- Ionic compounds conduct electricity only when molten or in solution, as ions can move freely. In the solid state, ions are fixed in position.
- Metallic compounds are malleable; metal layers can slide when a force is applied, and metallic bonds reform.
- The attractive forces between metal ions and delocalized electrons act in all directions.
- Metallic compounds are strong and hard due to strong attractive forces between metal ions and delocalized electrons.
- Metals have high melting and boiling points because of these strong attractive forces.
- A greater number of delocalized electrons and smaller cation size result in greater attractive force and higher melting/boiling points.
- Pure metals are insoluble in water.
- Metals conduct electricity in solid and liquid states because mobile electrons can move freely.
Covalent Bonding & Simple Covalent Lattice Structures
- Simple covalent lattices have low melting and boiling points because of weak intermolecular forces.
- Little energy is needed to break the lattice.
- Most compounds are insoluble in water unless they are polar (like HCl) or can form hydrogen bonds (like NH3).
- They do not conduct electricity in solid or liquid states due to the absence of charged particles.
- Some simple covalent compounds conduct electricity in solution (e.g., HCl forms H+ and Cl− ions).
Covalent Bonding & Giant Covalent Lattice Structures
- Giant covalent lattices have high melting and boiling points because of a large number of covalent bonds linking the entire structure.
- A lot of energy is required to break the lattice.
- The compounds can vary in hardness.
- Graphite is soft due to weak forces between carbon layers.
- Diamond and silicon(IV) oxide are hard due to their 3D network of strong covalent bonds.
- Most compounds are insoluble in water.
- Most compounds do not conduct electricity, but some exceptions exist.
- Graphite has delocalized electrons between carbon layers that can move when a voltage is applied.
- Diamond and silicon(IV) oxide do not conduct electricity because all outer electrons are involved in covalent bonds.
Characteristics Comparison Table
| Characteristic | Giant Ionic | Giant Metallic | Simple Covalent | Giant Covalent |
|---|
| Melting/Boiling Points | High | Moderately high to high | Low | Very high |
| Electrical Conductivity | Only when molten/solution | When solid or liquid | Do not conduct electricity | Do not conduct electricity (except graphite) |
| Solubility | Soluble | Insoluble (some may react) | Usually insoluble unless they are polar | Insoluble |
| Hardness | Hard, brittle | Hard, malleable | Soft | Very hard (diamond/SiO2) or soft (graphite) |
| Physical State | Solid | Solid | Solid, liquid, gas | Solid |
| Forces | Electrostatic attraction | Delocalised sea of electrons attracting positive ions | Weak intermolecular forces between molecules | Electrons in covalent bonds between atoms |
| Particles | Ions | Positive ions in a sea of electrons | Small molecules | Atoms |
| Example | NaCl | Copper | Br2 | Graphite, silicon(IV) oxide |
Example Problem
- Problem: Given the physical properties of substances X, Y, and Z, identify their structure.
- Solution:
- X (Melting Point: 839°C, Conductivity: Good when molten, Solubility: Soluble) - likely a giant ionic structure.
- Y (Melting Point: 95°C, Conductivity: Very poor, Solubility: Almost insoluble) - likely a simple molecular structure.
- Z (Melting Point: 1389°C, Conductivity: Good, Solubility: Insoluble) - likely a giant metallic structure.
Gas Pressure
- Gases exert pressure due to gas molecules colliding with the container walls.
Changing Gas Volume:
- Decreasing volume (at constant temperature) increases pressure due to more frequent collisions.
- Volume is inversely proportional to pressure at constant temperature.
Changing Gas Temperature:
- Increasing temperature (at constant volume) increases pressure as molecules gain kinetic energy and collide more frequently.
- Temperature is directly proportional to pressure at constant volume.
Ideal Gases
Kinetic Theory of Gases:
- Gas molecules are constantly moving randomly.
- Molecules have negligible volume.
- No intermolecular forces exist.
- Collisions are elastic (no kinetic energy loss).
- Temperature is related to average kinetic energy.
- Gases following these rules are called ideal gases; real gases approximate this.
Ideal Gas Law:
- Volume depends on pressure and temperature.
- Heating a gas (at constant pressure) increases volume as particles gain kinetic energy and collide more frequently.
- Volume is directly proportional to temperature.
Limitations of the Ideal Gas Law:
- Real gases deviate at high pressures and low temperatures because:
- Molecules are closer together.
- Intermolecular forces become significant.
- Molecular volume is no longer negligible.
- Assumptions of no intermolecular forces and negligible volume break down.
- Attractive forces reduce impact force, lowering measured pressure.
Equations