Topic 1: Atomic Structure
AS Level · Physical Chemistry · CIE 9701 · 2025–2027 syllabus
Topic 1: Atomic Structure
The foundation of all chemistry — understanding the subatomic particles, electron arrangement, and nuclear notation that underpin every topic that follows. Tested in Paper 1 (MCQ) and Paper 2 (Structured). Key skills: writing electron configurations, interpreting mass spectra, explaining ionisation energy trends.
What this topic covers
Key particles at a glance
| Particle | Symbol | Relative Mass | Relative Charge | Location |
|---|---|---|---|---|
| Proton | p⁺ | 1 | +1 | Nucleus |
| Neutron | n⁰ | 1 | 0 | Nucleus |
| Electron | e⁻ | 1/1840 (≈ 0) | −1 | Shells / orbitals |
Full revision notes · aligned with 9701 syllabus learning outcomes
Revision Notes
A. Nuclear Notation & Isotopes
Every atom is represented as ᴬZX, where A = mass number (protons + neutrons) and Z = atomic number (protons). The number of neutrons = A − Z.
B. Mass Spectrometry
A mass spectrometer separates ions by their mass-to-charge (m/z) ratio. The key steps are:
- 1. VaporiseSample is vaporised into gaseous atoms/molecules.
- 2. IoniseHigh-energy electrons knock out one electron from each atom → positive ions (M⁺).
- 3. AccelerateElectric field accelerates ions to the same kinetic energy.
- 4. DeflectMagnetic field deflects ions — lighter ions deflect more, heavier ions deflect less.
- 5. DetectDetector records the m/z and relative abundance of each ion.
C. Electron Configuration
Electrons occupy subshells in order of increasing energy. The four rules to follow:
Common electron configurations (Period 1–3 + key exceptions)
D. Ionisation Energy
The first ionisation energy (1st IE) is the energy required to remove one mole of electrons from one mole of gaseous atoms to form one mole of gaseous 1+ ions:
Successive ionisation energies increase because each subsequent electron is removed from an increasingly positive ion. A large jump between successive IEs indicates that the next electron is being removed from a new (inner) shell — this is how you can deduce the group of an element.
Fully worked solutions with examiner mark scheme annotations
Worked Examples
- Multiply each isotope's mass by its percentage abundance:
¹⁰B: 10 × 19.9 = 199 · ¹¹B: 11 × 80.1 = 881.1 - Sum the results: 199 + 881.1 = 1080.1
- Divide by 100: 1080.1 ÷ 100 = 10.801
- Round to 1 d.p.: Aᵣ = 10.8
- Write the ground state configuration of Cu (note the exception): Cu = [Ar] 3d¹⁰ 4s¹
- Cu²⁺ has lost 2 electrons. Remove from the highest energy subshell first — 4s before 3d.
- Remove 1 electron from 4s¹ → [Ar] 3d¹⁰ (Cu⁺)
- Remove 1 more electron from 3d¹⁰ → [Ar] 3d⁹ (Cu²⁺)
- Look for the large jump in successive IEs: the jump occurs between the 4th IE (6220) and 5th IE (37 800).
- The large jump means the 5th electron is being removed from an inner shell (much closer to the nucleus).
- Therefore, there are 4 electrons in the outer shell → X is in Group 14.
- Atomic number Z = 26 → number of protons = 26
- Neutral atom → number of electrons = number of protons = 26
- Number of neutrons = A − Z = 56 − 26 = 30
Paper 1 · Paper 2 · Command words · Mark scheme language
Exam Technique
- State the full equation for 1st IE: X(g) → X⁺(g) + e⁻ with state symbols
- Use "per mole" language when defining IE: "energy to remove one mole of electrons from one mole of gaseous atoms"
- Show all working in Aᵣ calculations — method marks are available even for a wrong answer
- Reference "greater nuclear attraction" or "less shielding" when explaining IE trends — vague answers score 0
- For electron config of ions, remove electrons from highest energy subshell first (4s before 3d)
- Don't write Cu as [Ar] 3d⁹ 4s² — the exception is [Ar] 3d¹⁰ 4s¹
- Don't omit state symbols in ionisation energy equations
- Don't confuse mass number (A) with atomic mass (Aᵣ) — they are different quantities
- Don't say "more electrons" when explaining why IE decreases down a group — specify shielding and distance from nucleus
- Don't use "shells" when "subshells" or "orbitals" is needed for full marks
Key command words for this topic
High-mark definition: First Ionisation Energy
Equation (must include state symbols): X(g) → X⁺(g) + e⁻
Common mark scheme catches: missing "gaseous", missing "per mole", missing state symbols, or writing it as an exothermic process (it is always endothermic — ΔH is positive).
All learning outcomes from the 9701 syllabus (2025–2027) · tick off as you revise
Syllabus Checklist
1.1 Subatomic particles & nuclear notation
- Identify and describe protons, neutrons and electrons in terms of relative charge and relative mass
- Deduce the number of protons, neutrons and electrons in atoms and ions given the atomic number, mass number and charge
- Describe the distribution of mass and charge within an atom
- Define the term isotope
1.2 Relative atomic mass & mass spectrometry
- Define the terms relative isotopic mass and relative atomic mass (in terms of ¹²C)
- Describe the operation of a mass spectrometer (ionisation, acceleration, deflection, detection)
- Interpret a simple mass spectrum to calculate relative atomic mass
- Calculate Aᵣ from % abundance and isotopic masses
1.3 Electron configuration
- Describe the number of electrons in s, p and d subshells and in s, p and d orbitals
- Describe the shapes of s and p orbitals
- State the Aufbau principle, Hund's rule and the Pauli exclusion principle
- Write full electron configurations for atoms and ions (including transition metals)
- Explain the anomalous configurations of Cr and Cu
- Write abbreviated (noble gas core) electron configurations
1.4 Ionisation energy
- Define first ionisation energy; write and interpret the equation for 1st IE
- Explain the general trend in first ionisation energies across Period 2 and Period 3
- Explain the dip in 1st IE between Groups 2→3 (new subshell) and 5→6 (electron pairing)
- Explain the trend in first ionisation energies down a group
- Explain how successive ionisation energies provide evidence for shell structure
- Deduce the group of an element from its successive ionisation energy data