Introduction
Electronic configuration describes how electrons are distributed among the orbitals of an atom. Three fundamental rules govern this distribution.
The Three Rules
1. Aufbau Principle
“Building up” - Electrons fill orbitals in order of increasing energy.
$$1s < 2s < 2p < 3s < 3p < 4s < 3d < 4p < 5s < 4d < 5p < 6s < 4f < 5d < 6p < 7s < 5f < 6d < 7p$$The (n + l) Rule
Orbitals fill in order of increasing (n + l). If (n + l) is same, lower n fills first.
| Orbital | n | l | n + l | Filling order |
|---|---|---|---|---|
| 3d | 3 | 2 | 5 | Later |
| 4s | 4 | 0 | 4 | Earlier |
| 4p | 4 | 1 | 5 | After 3d |
| 5s | 5 | 0 | 5 | After 4p |
2. Pauli’s Exclusion Principle
“No two electrons can have identical set of all four quantum numbers.”
Consequences:
- Maximum 2 electrons per orbital
- Must have opposite spins (↑↓)
- Maximum electrons in:
- Subshell: 2(2l + 1)
- Shell: 2n²
| Subshell | Max electrons |
|---|---|
| s | 2 |
| p | 6 |
| d | 10 |
| f | 14 |
3. Hund’s Rule of Maximum Multiplicity
“Electrons occupy degenerate orbitals singly with parallel spins before pairing.”
For 3 electrons in p orbitals:
Correct: ↑ | ↑ | ↑ (parallel spins)
Wrong: ↑↓ | ↑ | (premature pairing)
Reason: Parallel spins in different orbitals minimize electron-electron repulsion.
Writing Electronic Configurations
Standard Notation
Example: Oxygen (Z = 8)
$$1s^2 \, 2s^2 \, 2p^4$$Noble Gas Core Notation
Example: Iron (Z = 26)
$$[\text{Ar}] \, 3d^6 \, 4s^2$$where [Ar] = $1s^2 2s^2 2p^6 3s^2 3p^6$
Orbital Box Notation
For nitrogen (Z = 7):
| 1s | 2s | 2p |
|---|---|---|
| ↑↓ | ↑↓ | ↑ | ↑ | ↑ |
Electronic Configurations of Elements
First 30 Elements
| Z | Element | Configuration |
|---|---|---|
| 1 | H | 1s¹ |
| 2 | He | 1s² |
| 3 | Li | [He] 2s¹ |
| 4 | Be | [He] 2s² |
| 5 | B | [He] 2s² 2p¹ |
| 6 | C | [He] 2s² 2p² |
| 7 | N | [He] 2s² 2p³ |
| 8 | O | [He] 2s² 2p⁴ |
| 9 | F | [He] 2s² 2p⁵ |
| 10 | Ne | [He] 2s² 2p⁶ |
| 11 | Na | [Ne] 3s¹ |
| 18 | Ar | [Ne] 3s² 3p⁶ |
| 19 | K | [Ar] 4s¹ |
| 20 | Ca | [Ar] 4s² |
| 21 | Sc | [Ar] 3d¹ 4s² |
| 26 | Fe | [Ar] 3d⁶ 4s² |
| 29 | Cu | [Ar] 3d¹⁰ 4s¹ (Exception!) |
| 30 | Zn | [Ar] 3d¹⁰ 4s² |
Exceptional Configurations
Why Exceptions Occur
Half-filled and fully-filled subshells have extra stability due to:
- Exchange energy: More for parallel electrons
- Symmetry: Even distribution of electrons
Common Exceptions
Chromium (Z = 24)
- Expected: [Ar] 4s² 3d⁴
- Actual: [Ar] 4s¹ 3d⁵ (half-filled d)
Copper (Z = 29)
- Expected: [Ar] 4s² 3d⁹
- Actual: [Ar] 4s¹ 3d¹⁰ (fully-filled d)
Interactive Demo: Visualize Electronic Configuration
See how electrons fill orbitals following the Aufbau principle, Pauli exclusion, and Hund’s rule. Explore exceptional configurations of Cr and Cu.
Other Exceptions (for reference)
| Element | Z | Expected | Actual | Reason |
|---|---|---|---|---|
| Mo | 42 | [Kr] 5s² 4d⁴ | [Kr] 5s¹ 4d⁵ | Half-filled |
| Ag | 47 | [Kr] 5s² 4d⁹ | [Kr] 5s¹ 4d¹⁰ | Fully-filled |
| Au | 79 | [Xe] 6s² 4f¹⁴ 5d⁹ | [Xe] 6s¹ 4f¹⁴ 5d¹⁰ | Fully-filled |
Configurations of Ions
Cations (Positive ions)
Electrons are removed from outermost shell first, not the last-filled orbital.
Example: Fe²⁺ (Z = 26)
- Fe: [Ar] 3d⁶ 4s²
- Fe²⁺: [Ar] 3d⁶ (4s electrons removed first!)
Example: Cu⁺
- Cu: [Ar] 3d¹⁰ 4s¹
- Cu⁺: [Ar] 3d¹⁰
Anions (Negative ions)
Electrons are added to the lowest available orbital.
Example: O²⁻
- O: [He] 2s² 2p⁴
- O²⁻: [He] 2s² 2p⁶ = [Ne]
For transition metal cations, 4s electrons are lost before 3d electrons, even though 4s fills before 3d!
Why? In ions, 3d has lower energy than 4s due to effective nuclear charge.
Magnetic Properties
From Electronic Configuration
- Unpaired electrons → Paramagnetic (attracted by magnet)
- All paired → Diamagnetic (weakly repelled by magnet)
Number of unpaired electrons:
| Ion | Configuration | Unpaired e⁻ | Magnetic |
|---|---|---|---|
| Fe²⁺ | [Ar] 3d⁶ | 4 | Paramagnetic |
| Fe³⁺ | [Ar] 3d⁵ | 5 | Paramagnetic |
| Cu⁺ | [Ar] 3d¹⁰ | 0 | Diamagnetic |
| Zn²⁺ | [Ar] 3d¹⁰ | 0 | Diamagnetic |
Problem Solving
Example 1: Write Configuration
Problem: Write the electronic configuration of V (Z = 23) and V³⁺.
Solution:
- V: [Ar] 3d³ 4s²
- V³⁺: [Ar] 3d² (remove 2 from 4s, then 1 from 3d)
Example 2: Identify Element
Problem: An element has configuration [Kr] 4d¹⁰ 5s² 5p⁴. Identify it.
Solution:
- Kr has Z = 36
- Add: 10 + 2 + 4 = 16 more electrons
- Total Z = 36 + 16 = 52
- Element: Tellurium (Te)
Example 3: Compare Stability
Problem: Which is more stable: [Ar] 3d⁵ 4s¹ or [Ar] 3d⁴ 4s²?
Solution: [Ar] 3d⁵ 4s¹ is more stable because:
- d⁵ is half-filled (extra stability)
- This is why Cr has this configuration
Quick Reference
Maximum Electrons
| Subshell | Formula | Max |
|---|---|---|
| s | 2(0)+1 = 1 orbital | 2 |
| p | 2(1)+1 = 3 orbitals | 6 |
| d | 2(2)+1 = 5 orbitals | 10 |
| f | 2(3)+1 = 7 orbitals | 14 |
Stable Configurations
- Fully filled: s², p⁶, d¹⁰, f¹⁴
- Half filled: p³, d⁵, f⁷
- Noble gas: Very stable
Practice Problems
Write the electronic configuration of Mn²⁺ and calculate unpaired electrons.
Element X has configuration [Ar] 3d⁵. What is its atomic number and is it a ground state configuration?
Which has more unpaired electrons: Fe²⁺ or Fe³⁺?
Why is Cu⁺ colorless while Cu²⁺ is blue?
What’s Next?
You’ve completed the Atomic Structure chapter! Key connections:
- Chemical Bonding - How atoms share/transfer electrons
- Periodic Properties - How configuration affects properties
Related Topics
Within Atomic Structure
- Quantum Numbers — The foundation for understanding orbitals
- Orbital Shapes — Visualizing where electrons are
Chemistry Connections
- Chemical Bonding — How configurations determine bonding
- Periodic Properties — Configuration explains trends
- d-Block Elements — Transition metal configurations
- Coordination Compounds — d-orbital involvement
Physics Connections
- Magnetism — Unpaired electrons cause paramagnetism
- Bohr Model — Historical context for energy levels