3.1.2
Trends in the Periodic Table
Atomic Radius
Atomic Radius
There are key trends in atomic radius as we go across periods and when we go down groups.
Periodic trend
Periodic trend
- Atomic radius decreases along a period.
- This is because the number of protons in the nucleus increases across the period.
- As you add protons, you also add electrons. But these are all being added to the same shell, so this does not affect the radius.
- So each electron feels a stronger attraction to the nucleus and is held closer.
Periodic example
Periodic example
- In Period 3, sulfur has a smaller atomic radius than phosphorus.
- Sulfur has one more electron but still only fills up the same shell (3p) as phosphorus, so the radius is not affected.
- But sulfur has one more proton than phosphorus - this does affect the radius.
- Sulfur has a greater nuclear charge because of having more protons.
- This pulls the electrons closer.
- This means the atomic radius is smaller.
Group trend
Group trend
- Atomic radius increases down a group.
- This is because the number of electron shells increases down a group.
- Each subsequent electron shell is further from the nucleus.
- This effect outweighs the increase in proton number down the group.
Group example
Group example
- In Group 2, magnesium has a larger radius than beryllium.
- Magnesium has more electrons than beryllium and they occupy an additional electron shell.
- The extra electron shell is further from the nucleus.
- So the atomic radius is larger.
Ionisation Energy
Ionisation Energy
We see trends in ionisation energy across the periods and down the groups of the periodic table.
Periodic trend
Periodic trend
- Ionisation energy increases along a period.
- This is because the electrostatic attraction of each electron to the nucleus increases.
- The attraction increases because the proton number increases.
Periodic example
Periodic example
- In Period 3, chlorine has a greater nuclear charge than sulfur because it has a greater proton number.
- So the electrostatic charge between electrons and the nucleus in chlorine will be greater.
- So the ionisation energy is greater.
Group trend
Group trend
- Ionisation energy decreases down a group.
- This is because the outer electron is further from the nucleus down the group.
- The electrostatic attraction of the outer electron to the nucleus decreases down the group.
Group example
Group example
- In Group 2, magnesium is below beryllium.
- Magnesium fills up an extra electron shell than beryllium.
- This means an electron is further from the nucleus in magnesium and so the electrostatic attraction is less.
- So the ionisation energy of magnesium is lower than beryllium.
Melting Points
Melting Points
There are clear trends in the melting points across periods and down groups in the periodic table. We look at Period 3 to see this trend.
Structure on melting point
Structure on melting point
- For metals:
- The greater the number of valence electrons, the greater the melting point.
- For covalent compounds:
- Molecular solids have low melting points.
- Giant covalent structures have relatively high melting points.
Period trend
Period trend
- As you move along a period, you go from metals to giant covalent structures, to molecular solids.
- Using our knowledge of melting points of different structures from the previous slide:
- The melting points increase, peak sharply, and then decrease.
- We will look at Period 3 to showcase this trend.
Na, Mg, Al
Na, Mg, Al
- These all have metallic structures.
- Melting point and boiling point increase from Na to Al.
- This is because each element donates one more electron to the sea of free electrons.
- The electrostatic attractions are greater, so the melting point rises.
Si
Si
- Silicon has the highest melting point.
- This is because it has a giant covalent structure.
- To melt silicon, you must break strong covalent bonds, which requires a lot of energy.
P, S, Cl, Ar
P, S, Cl, Ar
- These elements are simple molecules.
- They are held together by Van der Waals forces.
- Sulfur has the highest melting point of the four because it exists as molecules of S8.
- This means it has a lot of electrons per molecule, so has stronger Van der Waals attractions.
- By contrast, P exists as P4 and Cl exists as Cl2.
1Physical Chemistry
1.1Atomic Structure
1.1.1Fundamental Particles
1.1.2Isotopes & Mass Number
1.1.3Mass Spectrometry
1.1.4Electron Shells, Sub-Shells & Orbitals
1.1.5Electron Configuration
1.1.6Ionisation Energy
1.1.7Factors Affecting Ionisation Energies
1.1.8Trends of Ionisation
1.1.9Specific Impacts on Ionisation Energies
1.1.10End of Topic Test - Atomic Structure
1.1.11A-A* (AO3/4) - Atomic Structure
1.2Amount of Substance
1.3Bonding
1.3.1Ionic Bonding
1.3.2Covalent & Dative Bonding
1.3.3Carbon Structures
1.3.4Metallic Bonding
1.3.5Physical Properties
1.3.6Shapes of Molecules
1.3.7Polarity
1.3.8Intermolecular Forces
1.3.9Intermolecular Forces 2
1.3.10End of Topic Test - Bonding
1.3.11Exam-Style Question - Shape of Molecules
1.3.12A-A* (AO3/4) - Bonding
1.4Energetics
1.5Kinetics
1.6Equilibria
2Physical Chemistry 2 (A2 Only)
2.1Thermodynamics (A2 Only)
2.2Rate Equations (A2 Only)
2.3The Equilibrium Constant Kp (A2 Only)
2.4Electrochemical Cells (A2 Only)
2.5Acids & Bases (A2 Only)
2.5.1Brønsted-Lowry Acids & Bases (A2 Only)
2.5.2pH (A2 Only)
2.5.3The Ionic Product of Water (A2 Only)
2.5.4Weak Acids & Bases (A2 Only)
2.5.5pH Curves & Titrations (A2 Only)
2.5.6pH Curves & Titrations 2 (A2 Only)
2.5.7Buffer Solutions (A2 Only)
2.5.8End of Topic Test - Acids & Bases
2.5.9Exam-Style Question - Weak Acids
2.5.10A-A* (AO3/4) - Acids & Bases
3Inorganic Chemistry
3.1Periodicity & Trends
4Inorganic Chemistry 2 (A2 Only)
4.1Period 3 (A2 Only)
4.2Transition Metals (A2 Only)
4.2.1General Properties (A2 Only)
4.2.2Substitution Reactions (A2 Only)
4.2.3Shapes of Complex Ions (A2 Only)
4.2.4Colours of Ions (A2 Only)
4.2.5Variable Oxidation States (A2 Only)
4.2.6Titrations (A2 Only)
4.2.7Homogeneous Catalysts (A2 Only)
4.2.8Heterogeneous Catalysts (A2 Only)
4.2.9End of Topic Test - Transition Metals
4.2.10A-A* (AO3/4) - Transition Metals
4.3Reactions of Ions in Aqueous Solutions (A2 Only)
5Organic Chemistry 1
5.1Introduction
5.2Alkanes
5.3Halogenoalkanes
5.4Alkenes
5.5Alcohols
5.6Organic Analysis
5.7A-A* (AO3/4) - Organic 1
6Organic Chemistry 2 (A2 Only)
6.1Optical Isomerism (A2 Only)
6.2Aldehydes & Ketones (A2 Only)
6.3Carboxylic Acids & Esters (A2 Only)
6.4Aromatic Chemistry (A2 Only)
6.5Amines (A2 Only)
6.6Polymers (A2 Only)
6.7Biological Organic (A2 Only)
6.8Organic Synthesis (A2 Only)
6.9NMR Spectroscopy (A2 Only)
6.10Chromatography (A2 Only)
6.11A-A* (AO3/4) - Organic 2
Jump to other topics
1Physical Chemistry
1.1Atomic Structure
1.1.1Fundamental Particles
1.1.2Isotopes & Mass Number
1.1.3Mass Spectrometry
1.1.4Electron Shells, Sub-Shells & Orbitals
1.1.5Electron Configuration
1.1.6Ionisation Energy
1.1.7Factors Affecting Ionisation Energies
1.1.8Trends of Ionisation
1.1.9Specific Impacts on Ionisation Energies
1.1.10End of Topic Test - Atomic Structure
1.1.11A-A* (AO3/4) - Atomic Structure
1.2Amount of Substance
1.3Bonding
1.3.1Ionic Bonding
1.3.2Covalent & Dative Bonding
1.3.3Carbon Structures
1.3.4Metallic Bonding
1.3.5Physical Properties
1.3.6Shapes of Molecules
1.3.7Polarity
1.3.8Intermolecular Forces
1.3.9Intermolecular Forces 2
1.3.10End of Topic Test - Bonding
1.3.11Exam-Style Question - Shape of Molecules
1.3.12A-A* (AO3/4) - Bonding
1.4Energetics
1.5Kinetics
1.6Equilibria
2Physical Chemistry 2 (A2 Only)
2.1Thermodynamics (A2 Only)
2.2Rate Equations (A2 Only)
2.3The Equilibrium Constant Kp (A2 Only)
2.4Electrochemical Cells (A2 Only)
2.5Acids & Bases (A2 Only)
2.5.1Brønsted-Lowry Acids & Bases (A2 Only)
2.5.2pH (A2 Only)
2.5.3The Ionic Product of Water (A2 Only)
2.5.4Weak Acids & Bases (A2 Only)
2.5.5pH Curves & Titrations (A2 Only)
2.5.6pH Curves & Titrations 2 (A2 Only)
2.5.7Buffer Solutions (A2 Only)
2.5.8End of Topic Test - Acids & Bases
2.5.9Exam-Style Question - Weak Acids
2.5.10A-A* (AO3/4) - Acids & Bases
3Inorganic Chemistry
3.1Periodicity & Trends
4Inorganic Chemistry 2 (A2 Only)
4.1Period 3 (A2 Only)
4.2Transition Metals (A2 Only)
4.2.1General Properties (A2 Only)
4.2.2Substitution Reactions (A2 Only)
4.2.3Shapes of Complex Ions (A2 Only)
4.2.4Colours of Ions (A2 Only)
4.2.5Variable Oxidation States (A2 Only)
4.2.6Titrations (A2 Only)
4.2.7Homogeneous Catalysts (A2 Only)
4.2.8Heterogeneous Catalysts (A2 Only)
4.2.9End of Topic Test - Transition Metals
4.2.10A-A* (AO3/4) - Transition Metals
4.3Reactions of Ions in Aqueous Solutions (A2 Only)
5Organic Chemistry 1
5.1Introduction
5.2Alkanes
5.3Halogenoalkanes
5.4Alkenes
5.5Alcohols
5.6Organic Analysis
5.7A-A* (AO3/4) - Organic 1
6Organic Chemistry 2 (A2 Only)
6.1Optical Isomerism (A2 Only)
6.2Aldehydes & Ketones (A2 Only)
6.3Carboxylic Acids & Esters (A2 Only)
6.4Aromatic Chemistry (A2 Only)
6.5Amines (A2 Only)
6.6Polymers (A2 Only)
6.7Biological Organic (A2 Only)
6.8Organic Synthesis (A2 Only)
6.9NMR Spectroscopy (A2 Only)
6.10Chromatography (A2 Only)
6.11A-A* (AO3/4) - Organic 2
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