Why do the properties of the elements change in regular patterns across the periodic table?
The trends in covalent radius, first ionisation energy and electronegativity across periods and down groups, explained in terms of nuclear charge, number of occupied shells and the screening effect of inner electrons.
An SQA Higher Chemistry answer on periodic trends, explaining how covalent radius, first ionisation energy and electronegativity change across periods and down groups in terms of nuclear charge, the number of occupied electron shells and the screening effect of inner electrons.
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What this key area is asking
The SQA wants you to explain, not just state, the periodic trends. You must account for the changes in covalent radius, first ionisation energy and electronegativity using three ideas: nuclear charge, the number of occupied electron shells, and the screening effect of inner electron shells. "Explain fully" questions here demand that all three factors are weighed against each other, so this key area rewards careful, complete wording.
The three explaining factors
Across a period
Going left to right, protons are added to the nucleus while electrons fill the same outer shell, so screening barely changes.
- Covalent radius decreases: the increasing nuclear charge pulls the same shell of electrons closer.
- First ionisation energy increases: the outer electrons are held more tightly, so more energy is needed to remove one.
- Electronegativity increases: the smaller, more positively charged atom attracts bonding electrons more strongly.
Down a group
Going down a group, each element has an extra occupied shell and more screening inner electrons.
- Covalent radius increases: the outer electrons occupy a higher shell, further from the nucleus.
- First ionisation energy decreases: the outer electron is further away and more screened, so it is easier to remove.
- Electronegativity decreases: the bonding electrons sit further from the nucleus and feel less pull.
Ionisation energy as an equation
Worked example: total ionisation energy
Putting it together
The key insight is that the extra shells and screening down a group outweigh the rising nuclear charge, whereas across a period the rising nuclear charge dominates because no new shell is added.
Examples in context
The periodic trends are not just exam abstractions; they drive real chemistry. The high electronegativity of fluorine (top right of the table, smallest atom) is why hydrogen fluoride forms strong hydrogen bonds and why bonds in materials such as PTFE are so unreactive. At the other extreme, the low ionisation energy of caesium, the easiest stable element to ionise, is exploited in photoelectric cells and atomic clocks, where a tiny amount of energy frees its loosely held outer electron. The steady fall in ionisation energy down Group 1 is also why reactivity with water increases from lithium to potassium: the more easily the single outer electron is lost, the more vigorous the redox reaction.
Try this
Q1. Explain why the first ionisation energy increases across period 3 from sodium to argon. [2 marks]
- Cue. The nuclear charge increases while electrons fill the same shell, so the outer electrons are held more tightly and need more energy to remove.
Q2. Account for the increase in covalent radius down Group 7. [2 marks]
- Cue. Each element has an extra occupied shell and more screening, placing the outer electrons further from the nucleus.
Q3. The first two ionisation energies of calcium are and . Calculate the energy to convert of into . [2 marks]
- Cue. .
Exam-style practice questions
Practice questions written in the style of SQA exam questions on this dot point, with worked answer explainers. The year tag is the paper they imitate, not the source.
SQA Higher 20183 marksExplain fully why the first ionisation energy decreases down Group 1 from lithium to caesium. Refer to nuclear charge, the number of occupied shells and screening in your answer.Show worked answer →
Markers want all three factors weighed against each other, not just distance.
Going down Group 1, each successive element has an additional occupied electron shell, so the outer electron is held in a shell that is further from the nucleus. There are also more inner electron shells, which screen (shield) the outer electron from the full attraction of the nucleus.
Although the nuclear charge (number of protons) increases down the group, the effects of the extra shell and the increased screening outweigh it, so the outer electron is held less tightly. Less energy is therefore needed to remove it, and the first ionisation energy decreases.
A common mark lost is quoting only "the atom is bigger" without naming the extra occupied shell and the increased screening, or forgetting to acknowledge that nuclear charge rises but is outweighed.
SQA Higher 20224 marksThe first ionisation energy of magnesium is and its second ionisation energy is . (a) Write the equation, with state symbols, for the first ionisation energy of magnesium. (b) Calculate the energy required to convert of gaseous magnesium atoms entirely into ions.Show worked answer →
Part (a) tests the definition as an equation; part (b) is a two-ionisation calculation.
(a) The first ionisation energy refers to one mole of gaseous atoms losing one mole of electrons:
(b) Forming requires both the first and second ionisation energies. The total energy per mole is:
For :
Markers reward the state symbols in part (a) (a frequent loss) and adding both ionisation energies before scaling by the number of moles in part (b).
Related dot points
- The arrangement of elements in the periodic table by atomic number into groups and periods, the link between electron arrangement and chemical behaviour, and the meaning of covalent radius, ionisation energy and electronegativity.
An SQA Higher Chemistry answer on periodicity, covering how elements are arranged by atomic number into groups and periods, how electron arrangement explains chemical behaviour, and the three trends of covalent radius, ionisation energy and electronegativity.
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Sources & how we know this
- SQA Higher Chemistry Course Specification — SQA (2018)