IB Chemistry HL Topic 2 — Models of Bonding & Structure Paper 1 & 2 Higher level ~10 min read

Expansion of the Octet

Nitrogen can never make five bonds. Phosphorus, sitting directly below it, makes five without complaint. That single difference opens up seven new shapes, and the good news is that you already know how to work all of them out — the counting method has not changed at all.

📘 What you need to know

Why only some elements can do it

An atom in period 2 has only 2s and 2p orbitals available. Together those hold a maximum of eight electrons, and there is nowhere else to put any more — the 3s orbital is far too high in energy to bother with. The octet rule is not a preference for these elements; it is a hard limit.

From period 3 onwards there are also 3d orbitals, and they sit close enough in energy to be used. That gives sulfur, phosphorus, chlorine, iodine and xenon somewhere to put extra pairs, so they can accommodate ten or twelve electrons around them.

The rule that decides it period 2 → no d orbitals → maximum 8  |  period 3 and below → vacant d orbitals → 10 or 12 possible
If your Lewis formula ever puts ten electrons on nitrogen or oxygen, stop and recount. It is always a mistake. The same structure on phosphorus or sulfur is perfectly fine.

Counting works exactly as before

🧩 The method, unchanged

  1. Count the valence electrons, adjusting for any charge.
  2. Draw the skeleton and put one bonding pair between each joined pair of atoms.
  3. Give every outer atom its octet first. Fluorine and oxygen can never expand, so they always take exactly three lone pairs each (fluorine) or two (a doubly bonded oxygen).
  4. Everything left over goes on the central atom, even if that takes it past eight.
  5. Count the domains on the central atom and read off the geometry.

Five electron domains

Five domains spread out into a trigonal bipyramid: three in a flat triangle round the middle (equatorial, 120° apart) and two pointing straight up and down (axial, at 90° to the triangle). Swap bonds for lone pairs and you get four different molecular shapes.

The trigonal bipyramidal family
Five domains, one lone pair added each time Amber lobes are lone pairs, and they always take equatorial places PCl₅ SF₄ ClF₃ I₃⁻ trigonal bipyramidal seesaw T-shaped linear 5 bonds, 0 lone 4 bonds, 1 lone 3 bonds, 2 lone 2 bonds, 3 lone The domain geometry is trigonal bipyramidal in all four. Only the shape changes.
Notice the pattern going right: every lone pair you add removes one equatorial atom, and the name changes even though the underlying arrangement is identical.

🤔 Why do lone pairs choose equatorial positions?

An axial position has three neighbours at 90°. An equatorial position has only two at 90° (the axial ones), with the other two sitting comfortably at 120°. Since 90° contacts are the crowded ones, and lone pairs repel more strongly than bonding pairs, the lone pairs take the roomier equatorial spots and leave the tighter axial positions to the bonds.

Six electron domains

Six domains arrange themselves into an octahedron: four in a square round the middle, plus one above and one below, all at 90°. Removing bonds and adding lone pairs gives three shapes.

The octahedral family
Six domains, all at 90 degrees to each other Two lone pairs go opposite each other, flattening the molecule SF₆ BrF₅ XeF₄ octahedral square pyramidal square planar 6 bonds, 0 lone 5 bonds, 1 lone 4 bonds, 2 lone SF₆ and XeF₄ are both symmetrical, so both are nonpolar. BrF₅ is not.
XeF4 is a nice test of understanding: it has two lone pairs but is still nonpolar, because they sit directly opposite each other and the four bond dipoles cancel in the square plane.

The full list

MoleculeValence electronsBonding pairsLone pairs on centreMolecular geometry
PCl54050trigonal bipyramidal
SF43441seesaw
ClF32832T-shaped
I32223linear
SF64860octahedral
BrF54251square pyramidal
XeF43642square planar

🧠 A shortcut for the lone pairs on the centre

For a molecule AXn made of a central atom and n halogens, work out (valence electrons − 8n) ÷ 2. Every outer halogen takes 8 electrons in total (one bonding pair plus three lone pairs), so whatever is left over belongs to the central atom. For SF4: (34 − 32) ÷ 2 = 1 lone pair. Quick, and it always works.

Worked examples

WE 1

Draw the Lewis formula for ClF3 and deduce its shape

Step 1: count Cl: 7 + (3 × 7) = 28 electrons Step 2: bonds and outer octets Three Cl–F bonds use 6. Each F needs 3 lone pairs: 3 × 6 = 18. 28 − 6 − 18 = 4 electrons = 2 lone pairs on Cl Step 3: count domains 3 bonding + 2 lone = 5 domains → trigonal bipyramidal Step 4: place the lone pairs equatorially That leaves the two axial fluorines and one equatorial fluorine. T-shaped, with bond angles slightly under 90° chlorine ends up with 10 electrons — correct, because it is in period 3
WE 2

State the electron domain geometry, molecular geometry and F–Xe–F bond angle in XeF2

Step 1: count the valence electrons Xe: 8 + (2 × 7) = 22 electrons Step 2: use them up Two Xe–F bonds use 4. Each F takes 3 lone pairs: 2 × 6 = 12. 22 − 4 − 12 = 6 electrons = 3 lone pairs on Xe Step 3: domains and placement 2 bonding + 3 lone = 5 domains → trigonal bipyramidal All three lone pairs go equatorial, leaving the two fluorines axial — directly opposite. Trigonal bipyramidal domains, linear molecule, 180° three answers were asked for, so give all three explicitly
WE 3

Explain why SF6 exists but OF6 does not

Step 1: what SF6 requires Six bonding pairs means 12 electrons around the central atom. Step 2: why sulfur can manage it Sulfur is in period 3, so it has vacant 3d orbitals available to hold the extra pairs. Step 3: why oxygen cannot Oxygen is in period 2, with only 2s and 2p orbitals. Those hold a maximum of 8 electrons and there is no accessible d subshell. Only period 3 and below can expand the octet the same argument explains why NCl₅ does not exist while PCl₅ does

💡 Exam tips

⚠ Common mix-ups

Up next: Formal Charge — the tie-breaker you use when two Lewis formulas both look valid and you have to decide which one the examiner wants.

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