IB Chemistry HL Topic 3 — Classifying the Elements Paper 1 & 2 Core skill ~12 min read

Variable Oxidation States in Transition Elements (HL)

Sodium has one oxidation state. Manganese has seven. The difference is not that manganese has more electrons — it is that its outermost electrons all cost about the same to remove, so the atom has no strong preference about where to stop. This page is about the configurations that make that possible.

📘 What you need to know

The configurations, and the two rebels

Run through the first row and the pattern is boringly regular: scandium [Ar]3d14s2, titanium [Ar]3d24s2, vanadium [Ar]3d34s2, and so on. Then chromium breaks it, and later copper breaks it again.

The two elements that break the filling rule4s 3d Cr expected Cr actual Cu expected Cu actual↑↓ ↑↓ ↑↓ ↑↓ ↑↓ ↑↓ ↑↓ ↑↓ ↑↓ ↑↓ ↑↓half-filled 3d [Ar] 3d⁵ 4s¹ completely full 3d [Ar] 3d¹⁰ 4s¹One 4s electron shifts across to make the 3d half full or completely full. The energy gain from that arrangement outweighs the cost of promoting the electron.
Both exceptions do the same thing for the same reason. If you can explain chromium you can explain copper, and vice versa.

Forming ions: 4s goes first

This is the point that trips people up more than any other in the d-block. The 4s subshell fills before the 3d, but it also empties before the 3d.

There is no contradiction. Once electrons occupy the 4s, it becomes the outermost subshell, and it is pushed slightly higher in energy than the 3d by repulsion from the electrons already there. Ionisation always removes the outermost, highest-energy electrons, so 4s electrons leave first.

The rule to write down fill 4s first  →  but remove 4s first

So iron, [Ar]3d64s2, becomes Fe2+ = [Ar]3d6, and then Fe3+ = [Ar]3d5. Notice that Fe3+ ends up with a half-filled d sublevel, which is part of why the 3+ state of iron is so stable.

Write out the atom’s configuration first, every single time, then take electrons off it. Trying to jump straight to the ion’s configuration is where the mistakes live.

Which states each element reaches

The oxidation states you meet most oftenTi V Cr Mn Fe Co Ni Cu +7 +6 +5 +4 +3 +2 +1 Manganese reaches +7 by using all seven of its 4s and 3d electrons.The +2 and +3 states run right across the row.
Every one of these metals can in principle reach +2 by losing its two 4s electrons. The chart shows the states you actually meet in reactions and in exam questions.

Two more patterns are worth noticing. The higher states are more common on the left of the row and become harder to reach on the right, because the growing nuclear charge holds the 3d electrons more tightly. And ions in states of +3 and above are strongly polarising — small, highly charged, and therefore capable of distorting nearby anions, which gives their compounds noticeable covalent character.

The ionisation energy evidence

How do we know 4s and 3d really are close in energy? Look at the successive ionisation energies of a transition element. For sodium there is an enormous jump after the first electron, because the second must come from a full inner shell. For titanium or vanadium the first four or five values rise steadily with no dramatic jump at all.

That smooth rise means the electrons being removed are all coming from a similar energy level — which is exactly what “4s and 3d are close together” predicts, and it is why several oxidation states are chemically accessible instead of just one.

Worked examples

WORKED EXAMPLE

Write the full electron configuration of Fe3+.

Step 1: the atom first Iron has 26 electrons. Fe: 1s² 2s² 2p⁶ 3s² 3p⁶ 3d⁶ 4s² Step 2: remove the 4s electrons Two go from 4s, giving Fe2+. Step 3: remove one more, now from 3d Fe³⁺: 1s² 2s² 2p⁶ 3s² 3p⁶ 3d⁵ [Ar] 3d⁵ — a half-filled d sublevel, which is why Fe3+ is so stable 23 electrons in total; check by adding the superscripts
WORKED EXAMPLE

Explain why chromium’s configuration is [Ar]3d54s1 rather than [Ar]3d44s2, and give the configuration of Cr3+.

Step 1: explain the exception Promoting one 4s electron to 3d gives a half-filled d sublevel with one electron in each of the five orbitals. Step 2: why that is preferred The 4s and 3d are so close in energy that the extra stability of the half-filled arrangement more than pays for the promotion. Step 3: form the ion Remove the single 4s electron first, then two 3d electrons. [Ar] 3d⁵ 4s¹ → [Ar] 3d³ Cr3+ is [Ar] 3d3 chromium only has one 4s electron to lose, so the second and third come from 3d
WORKED EXAMPLE

Explain why manganese can reach an oxidation state of +7 but nickel cannot.

Step 1: count the available electrons Mn: [Ar] 3d⁵ 4s² → 5 + 2 = 7 electrons outside the argon core Ni: [Ar] 3d⁸ 4s² → 8 + 2 = 10 electrons Step 2: why nickel has fewer options despite having more electrons Nickel has a higher nuclear charge, so its 3d electrons are held much more tightly and removing more than two costs far too much energy. Step 3: the limit The maximum state is set by how many electrons can realistically be removed, not by how many exist. Mn uses all seven of its outer electrons to reach +7; Ni is effectively limited to +2 this is why the highest oxidation states appear on the left of the row and fade towards the right

💡 Exam tip

⚠ Common mix-up

Up next: Colour in Transition Metal Complexes (HL) — the last piece. Those partly filled d orbitals split apart when ligands arrive, and the gap that opens up turns out to be exactly the size of a photon of visible light.

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