3.2.1
Atomic & Ionic Radii
Trends in Atomic Radii
Trends in Atomic Radii
Trends are seen in atomic radii across periods and down groups as the strength of the attraction between the nucleus and the outer electrons changes.


Measuring atomic radii
Measuring atomic radii
- An atomic orbital is a mathematical function that gives a probability of locating an electron within a defined volume known as an atomic orbital.
- Due to the uncertainty principle, the limits of an atom are difficult to define and measurements of atomic radii are not straightforward.
- To overcome this, chemists measure half the distance between two bonded atoms.


Periodic trend
Periodic trend
- On going across a period, the effective nuclear charge increases as protons are added to the nucleus whilst electrons are added to the same principal energy level (constant shielding).
- Therefore the outer electrons experience a greater attraction by the nucleus, leading to a decrease in atomic radius.
- Example: Sodium is at the start of period 3 with 11 protons and an atomic radius of 1.86 x 10-10 m. Chlorine at the end of period 3 has 17 protons and a smaller atomic radius of 9.90 x 10-11 m.


Group trend
Group trend
- On going down a group an extra principal energy level is added to the atomic structure and therefore the atomic radius increases.
- The effective nuclear charge is constant for elements in the same group (although the nuclear charge increases so does the number of shielding electrons) so this does not influence the change in atomic radius on descending a group.
- Example: In group 1, lithium has two principal energy levels and an atomic radius of 1.57 x 10-10 m, whereas potassium has four principal energy levels and a larger atomic radius of 2.35 x 10-10 m.


Overall trend
Overall trend
- The overall trend in atomic radius is shown above.
Trends in Ionic Radii
Trends in Ionic Radii
Trends are seen in ionic radii across periods and down groups as the strength of the attraction between the nucleus and the outer electrons changes.


Ionic radius
Ionic radius
- Ionic radius increases on descending a group as the ions have the same charge, but more principal energy levels.
- The trend in ionic radii going across a period is a little more complicated as there are positive and negative ions to consider:


Ionic radius of positive ions
Ionic radius of positive ions
- Positive ions are smaller than their parent atom as the highest principal energy level is removed when forming the cation.
- From group 1 to group 14, in period 3, all ions have the same electron configuration (1s22s22p6).
- As nuclear charge increases there is greater attraction to the outer electrons and therefore ionic radius decreases from group 1 to 14.


Ionic radius of negative ions
Ionic radius of negative ions
- Negative ions are larger than their parent atom as electrons are added to the highest principal energy level, but the nuclear charge is unchanged. The increased repulsion between electrons in the negative ion causes electrons to move further apart and increases the radius.
- From group 15 to group 17, in period 3, all ions have the same electron configuration (1s22s22p63s23p6).
- As nuclear charge increases there is a greater attraction to the electrons and therefore ionic radius decreases from group 15 to group 17.


Overall periodic trend
Overall periodic trend
- The overall trend in ionic radius across a period is summarised above, using period 3 as an example.
1Structure - Models of the Particulate of Matter
1.1Introduction to the Particulate Model of Matter
1.2The Nuclear Atom
1.3Electron Configuration
1.4Counting Particles by Mass: The Mole
1.6Elements, Compounds & Mixtures
1.7States of Matter & Changes of State
1.8Reacting Masses &. Volumes
1.9Solutions
2Structure - Models of Bonding & Structure
2.1The Ionic Model
2.2The Covalent Model
2.3Covalent Structures
2.4The Metallic Model
2.5From Models to Materials
2.6Valence Electrons & Ionic Compounds
2.7Molecular Shape
3Structure - Classification of Matter
3.1The Periodic Table: Classification of Elements
3.2Periodic Trends
3.3Group 1 Alkali Metals
3.4Halogens
3.5Noble gases, group 18
3.6Functional Groups: Classification of Organic
3.7Functional Group Chemistry
3.8Alkanes
3.9Alcohols
4Reactivity - What Drives Chemical Reaction?
4.1Endothermic & Exothermic Reactions
4.2Enthalpy of Reaction, Formation, & Hess' Law
5Reactivity - How Much, How Fast & How Far?
5.1Kinetics
5.2Rates of Reaction
5.3Stoichometry
5.4Le Châtelier’s Principle
5.5Introduction to Equilibrium
5.6Equilibrium Constant
5.7Reaction Quotient & Equilibrium Constant
6Reactivity - The Mechanisms of Chemical Change
6.1Proton Transfer Reactions
6.2The pH Scale
6.3Strong & Weak Acids and Bases
6.4Acid Deposition
6.5Types of Organic Reactions
6.6Oxidation & Reduction
6.7Electrochemical Cells
6.9Acid-Base Titrations
6.9.1Titration Calculation Weak Acid & Strong Base
6.9.2Titration Experimental Detail
6.9.3Extended Response - Titration
6.9.4Titration Calculations
6.9.5Titration Curves
6.9.6Titration Calculation Strong Acid & Weak Base
6.9.7IB Multiple Choice - Titrations
6.9.8Polyprotic Acids
6.9.9Titration Calculations Strong Acid & Strong Base
6.9.10Titrations Curves 2
7Measurement, Data Processing & Analysis
7.1Uncertainties & Errors in Measurements & Results
7.2Graphical Techniques
7.3Spectroscopic Identification of Organic Compounds
7.4Infrared Spectroscpy
Jump to other topics
1Structure - Models of the Particulate of Matter
1.1Introduction to the Particulate Model of Matter
1.2The Nuclear Atom
1.3Electron Configuration
1.4Counting Particles by Mass: The Mole
1.6Elements, Compounds & Mixtures
1.7States of Matter & Changes of State
1.8Reacting Masses &. Volumes
1.9Solutions
2Structure - Models of Bonding & Structure
2.1The Ionic Model
2.2The Covalent Model
2.3Covalent Structures
2.4The Metallic Model
2.5From Models to Materials
2.6Valence Electrons & Ionic Compounds
2.7Molecular Shape
3Structure - Classification of Matter
3.1The Periodic Table: Classification of Elements
3.2Periodic Trends
3.3Group 1 Alkali Metals
3.4Halogens
3.5Noble gases, group 18
3.6Functional Groups: Classification of Organic
3.7Functional Group Chemistry
3.8Alkanes
3.9Alcohols
4Reactivity - What Drives Chemical Reaction?
4.1Endothermic & Exothermic Reactions
4.2Enthalpy of Reaction, Formation, & Hess' Law
5Reactivity - How Much, How Fast & How Far?
5.1Kinetics
5.2Rates of Reaction
5.3Stoichometry
5.4Le Châtelier’s Principle
5.5Introduction to Equilibrium
5.6Equilibrium Constant
5.7Reaction Quotient & Equilibrium Constant
6Reactivity - The Mechanisms of Chemical Change
6.1Proton Transfer Reactions
6.2The pH Scale
6.3Strong & Weak Acids and Bases
6.4Acid Deposition
6.5Types of Organic Reactions
6.6Oxidation & Reduction
6.7Electrochemical Cells
6.9Acid-Base Titrations
6.9.1Titration Calculation Weak Acid & Strong Base
6.9.2Titration Experimental Detail
6.9.3Extended Response - Titration
6.9.4Titration Calculations
6.9.5Titration Curves
6.9.6Titration Calculation Strong Acid & Weak Base
6.9.7IB Multiple Choice - Titrations
6.9.8Polyprotic Acids
6.9.9Titration Calculations Strong Acid & Strong Base
6.9.10Titrations Curves 2
7Measurement, Data Processing & Analysis
7.1Uncertainties & Errors in Measurements & Results
7.2Graphical Techniques
7.3Spectroscopic Identification of Organic Compounds
7.4Infrared Spectroscpy
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