MHT-CET Chemistry · Free notes
Coordination Compounds — MHT-CET Chemistry
Coordination Compounds is about two questions a paper in MHT-CET Chemistry and almost never HARD — three of its 139 past-year questions. It is a chapter of counting and naming: how many donor atoms a ligand offers and what charge it carries, whether a complex is homoleptic or heteroleptic, cationic or anionic, and the oxidation state and coordination number that turn a name into a formula. Then come the four structural isomerisms and cis–trans, and the bonding arithmetic — hybridisation, unpaired electrons, EAN, and the stability orders. Five pages in the book's order. Every PYQ is tagged.
The handout has every subtopic, worked example, formula and trap with answers shown. The formula sheet is the chapter’s formulas and traps alone, on one page.
Subtopic notes
Ligands: Denticity, Donor Atoms, Charge and Field Strength
39 PYQsA ligand is an ion or molecule that donates one or more electron pairs to the central metal; its denticity is the number of donor atoms it uses at once (monodentate chloro and cyano, bidentate oxalato and ethylenediamine, hexadentate EDTA), an ambidentate ligand such as nitrito or thiocyanato can bind through either of two atoms, its charge is neutral (ammine, aqua, carbonyl) or anionic (chloro, sulphato, oxalato), and its position in the spectrochemical series says how strongly it splits the metal's d orbitals.
Types of Complexes: Homoleptic or Heteroleptic, Cationic, Anionic or Neutral
17 PYQsA complex is homoleptic when all its ligands are the same kind and heteroleptic when they differ; its coordination sphere is cationic, anionic or neutral according to the sum of the metal's oxidation state and the ligand charges, and a salt may pair a complex cation with simple anions, a complex anion with simple cations, or a complex cation with a complex anion.
Oxidation State, Coordination Number, Werner's Counter Ions and IUPAC Names
23 PYQsThe oxidation state of the central metal is what is left after the ligand charges are subtracted from the sphere charge, its coordination number is the number of donor atoms bonded to it, only the ions outside the square bracket ionise in solution, and an IUPAC name lists the ligands alphabetically before the metal, gives the metal's oxidation state in Roman numerals and ends in -ate when the sphere is an anion.
Isomerism in Coordination Compounds: Structural and Geometric
12 PYQsCoordination isomers share a formula but differ either in which atoms are bonded to the metal — structural isomers: ionisation, solvate, linkage and coordination — or only in how the same ligands are arranged in space — stereoisomers: geometric (cis and trans) and optical.
Bonding in Complexes: Hybridisation, Magnetism, EAN and Stability
48 PYQsValence bond theory reads a complex's geometry and hybridisation from the metal's d-electron count and the ligand's field strength — a strong-field ligand pairs the d electrons and gives an inner-orbital, low-spin complex — the unpaired electrons left over fix the spin-only magnetic moment, the effective atomic number counts the electrons around the metal after the ligands donate, and the stability of complexes with one ligand follows the metal's charge and the Irving–Williams order.
Formula & revision sheet
11 formulas · 2 reference tables · 15 gotchas across all subtopics — the exam-eve cheat-sheet
Formula & revision sheet
11 formulas · 2 reference tables · 15 gotchas across all subtopics — the exam-eve cheat-sheet
Formulas (2)
Reference tables (1)
Neutral and Anionic Ligands by Name11 rows
| Ligand | Formula | Charge | Denticity |
|---|---|---|---|
| Ammine | NH₃ | 0 | 1 Ammine (NH₃) is neutral; amido (NH₂⁻) is anionic. |
| Aqua | H₂O | 0 | 1 |
| Carbonyl | CO | 0 | 1 |
| Ethylenediamine (en) | H₂NCH₂CH₂NH₂ | 0 | 2 |
| Chloro / bromo / iodo / fluoro | X⁻ | −1 | 1 |
| Cyano | CN⁻ | −1 | 1 (through C) |
| Nitro / nitrito | NO₂⁻ / ONO⁻ | −1 | 1, ambidentate |
| Thiocyanato / isothiocyanato | SCN⁻ / NCS⁻ | −1 | 1, ambidentate |
| Oxalato | C₂O₄²⁻ | −2 | 2 |
| Sulphato / carbonato | SO₄²⁻ / CO₃²⁻ | −2 | 1 (usually) |
| EDTA | (edta)⁴⁻ | −4 | 6 |
Watch out for (3)
- Counting all four oxygens of oxalate→ Denticity and Counting Donor Atoms
- Reading carbonyl or carbonato by the 'carbon'→ Neutral and Anionic Ligands by Name
- Ranking by charge→ Field Strength: the Spectrochemical Series
Watch out for (1)
- Calling a salt 'neutral' because the whole compound is→ Same Ligands or Mixed, and the Charge on the Sphere
Formulas (3)
Watch out for (5)
- Counting ligands instead of donor atoms→ Oxidation State and Coordination Number
- Reading -ous and -ic backwards→ Oxidation State and Coordination Number
- Counting every chlorine in the formula→ Counter Ions: What Precipitates with Silver Nitrate
- Ordering ligands by charge or by prefix→ From Name to Formula and Back
- Dropping the -ate or the oxidation state→ From Name to Formula and Back
Reference tables (1)
The Four Structural Isomerisms4 rows
| Isomerism | What differs | Example pair |
|---|---|---|
| Ionisation | Anion inside ↔ anion outside | [Co(NH₃)₅Br]SO₄ / [Co(NH₃)₅SO₄]Br |
| Solvate (hydrate) | Water inside ↔ water of crystallisation | [Cr(H₂O)₆]Cl₃ / [Cr(H₂O)₅Cl]Cl₂·H₂O |
| Linkage | Donor atom of an ambidentate ligand | –NO₂ / –ONO; –SCN / –NCS Only an ambidentate ligand can do this. |
| Coordination | Ligands swapped between cation and anion metals | [Co(NH₃)₆][Cr(CN)₆] / [Cr(NH₃)₆][Co(CN)₆] |
Watch out for (2)
- Calling a water swap 'ionisation'→ The Four Structural Isomerisms
- Reading MA₂B₂ as MA₂BC→ Geometric (cis–trans) Isomerism and the MA₂BC Type
Formulas (4)
- Hybridisation and Geometry from d Electrons and Field Strength · Hybridisation by coordination number
- Unpaired Electrons and the Spin-Only Magnetic Moment · Spin-only magnetic moment
- Effective Atomic Number (EAN) · EAN
- Stability of Complexes: Metal Charge and the Irving–Williams Order · Irving–Williams order (same ligand)
Watch out for (4)
- Calling every four-coordinate complex tetrahedral→ Hybridisation and Geometry from d Electrons and Field Strength
- Using the free-ion count for a strong-field complex→ Unpaired Electrons and the Spin-Only Magnetic Moment
- Adding one electron per ligand, or per bidentate ligand→ Effective Atomic Number (EAN)
- Ranking by atomic number→ Stability of Complexes: Metal Charge and the Irving–Williams Order
PYQ weightage by concept
13 concepts · 139 PYQs — where the marks actually sit, so you know what to drill first
PYQ weightage by concept
13 concepts · 139 PYQs — where the marks actually sit, so you know what to drill first
| Concept | PYQs | Share |
|---|---|---|
| Denticity and Counting Donor Atoms | 17 | 12% |
| Neutral and Anionic Ligands by Name | 10 | 7% |
| Field Strength: the Spectrochemical Series | 6 | 4% |
| Concept | PYQs | Share |
|---|---|---|
| Same Ligands or Mixed, and the Charge on the Sphere | 13 | 9% |
| Concept | PYQs | Share |
|---|---|---|
| Oxidation State and Coordination Number | 8 | 6% |
| From Name to Formula and Back | 5 | 4% |
| Counter Ions: What Precipitates with Silver Nitrate | 2 | 1% |
| Concept | PYQs | Share |
|---|---|---|
| The Four Structural Isomerisms | 4 | 3% |
| Geometric (cis–trans) Isomerism and the MA₂BC Type | 1 | 1% |
| Concept | PYQs | Share |
|---|---|---|
| Hybridisation and Geometry from d Electrons and Field Strength | 6 | 4% |
| Unpaired Electrons and the Spin-Only Magnetic Moment | 5 | 4% |
| Effective Atomic Number (EAN) | 5 | 4% |
| Stability of Complexes: Metal Charge and the Irving–Williams Order | 5 | 4% |
Test yourself on Coordination Compounds
20 past MHT-CET questions from this chapter, timed at 18 minutes and marked the way the exam marks it. You see your score and every answer the moment you finish. Free to start.