Coordination Compounds: Compounds in which a central metal atom/ion is bonded to a set of molecules or ions called ligands.
Metal can be transition or inner transition element, usually having vacant d-orbitals.
NEET focuses on types of ligands, coordination numbers, bonding, and applications rather than memorizing all reactions.
Key Concept: The properties of coordination compounds depend on metal, oxidation state, and type of ligands.
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1. Chemical Arithmetic |
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2. Structure of Atom |
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3. Chemical Bonding and Molecular Structure |
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4. Solutions |
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5. The Solid State |
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6. Gaseous State |
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7. Nuclear Chemisty |
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8. Chemical Equilibrium |
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9. Ionic Equilibrium |
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10. Thermodynamics |
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11. Chemical Kinetics |
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12. Electrochemistry |
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14. Surface Chemistry |
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15. Chemical Periodicity |
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16. General Principles Of Extraction Of Metals |
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17. Hydrogen |
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18. s and p-Block Elements |
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19. The d-and f-Block Elements |
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20. Co-Ordination Chemistry |
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21. Chemical Analysis |
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22. Purification, Classification & Nomenclature Of Organic Compounds |
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23. Organic Chemistry – Some Basic Principles & Techniques |
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24. Hydrocarbons |
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25. Halogen Containing Compounds |
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26. Alcohols, Phenols and Ethers |
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27. Aldehydes And Ketones |
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28. Carboxylic Acids & Their Derivatives |
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29. Nitrogen Containing Compounds |
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30. Polymers |
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31. Biomolecules |
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32. Chemistry In Action |
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33. Chemistry Formula PDF for Entrance Exam |
Usually a transition metal, can have variable oxidation states.
Must have empty orbitals to accommodate ligands.
Properties influenced by size, charge, and electronic configuration.
NEET Focus: Conceptual understanding of why transition metals form complex compounds.
Definition: Species (ions or molecules) that donate one or more pairs of electrons to a central metal atom/ion.
Classification:
Monodentate ligands: donate 1 pair of electrons (e.g., NH₃, Cl⁻)
Bidentate ligands: donate 2 pairs of electrons (e.g., ethylenediamine, oxalate)
Polydentate ligands (Chelates): donate multiple electron pairs (e.g., EDTA⁴⁻)
Conceptual Focus: Understand chelation → enhanced stability of complex.
Definition: Number of ligand donor atoms directly bonded to the central metal atom.
Common numbers: 2, 4, 6
2 → Linear (e.g., [Ag(NH₃)₂]⁺)
4 → Tetrahedral/Square Planar (e.g., [Ni(CO)₄], [Pt(NH₃)₄]²⁺)
6 → Octahedral (e.g., [Fe(CN)₆]³⁻)
NEET Tip: Focus on how ligand size, metal size, and electronic configuration determine geometry.
Rules:
Name ligands first (alphabetical order), then metal
Use prefixes to indicate the number of ligands (di-, tri-, tetra-)
Oxidation state of metal in Roman numerals in parentheses
Examples:
[Co(NH₃)₆]Cl₃ → Hexaamminecobalt(III) chloride
[Cu(CN)₄]³⁻ → Tetracyanocuprate(I)
NEET Focus: Understanding nomenclature conceptually helps in solving reasoning-based questions.
1. Werner’s Theory:
Metal has primary and secondary valencies (oxidation state and coordination number)
Explained structural isomerism and bonding in complexes
2. Valence Bond Theory (VBT):
Ligands donate electron pairs to metal’s hybrid orbitals
Explains geometry (octahedral, tetrahedral, square planar)
Conceptual focus: d²sp³, sp³d², dsp² hybridization
3. Crystal Field Theory (CFT):
Metal-ligand interaction is electrostatic
d-Orbitals split in energy depending on geometry
Explains color, magnetic properties, and stability
Octahedral → d-orbital split into t₂g & eg
Tetrahedral → opposite splitting pattern
NEET Tip: Focus conceptually on why octahedral and tetrahedral complexes are colored (d-d transitions).
Structural Isomerism:
Ionization Isomerism → Different ions in solution (e.g., [Co(NH₃)₅Br]SO₄ vs [Co(NH₃)₅SO₄]Br)
Coordination Isomerism → Ligands exchanged between metal ions
Linkage Isomerism → Ligand attached through different atoms (e.g., SCN⁻ through S or N)
Hydrate Isomerism → Water molecules inside or outside coordination sphere
Stereoisomerism:
Geometrical Isomerism: cis/trans arrangement in square planar or octahedral complexes
Optical Isomerism: Non-superimposable mirror images
NEET Tip: Conceptually link ligand orientation → type of isomer.
1. Chelate Effect:
Polydentate ligands → higher stability due to ring formation
Example: EDTA forms very stable complexes with Ca²⁺, Fe³⁺
2. Factors Affecting Stability:
Nature of metal (charge, size, electronic configuration)
Nature of ligand (size, charge, denticity)
Geometrical constraints
Conceptual Focus: NEET often asks why chelates are more stable than monodentate complexes.
Analytical Chemistry:
EDTA titrations for metal ions
[Fe(CN)₆]³⁻ and [Fe(CN)₆]⁴⁻ in redox reactions
Medicine:
Cisplatin ([Pt(NH₃)₂Cl₂]) → Anti-cancer drug
Vitamin B₁₂ (Cobalt complex) → Essential for metabolism
Industrial Applications:
Catalysis: [Ni(CO)₄], [V₂O₅] complexes
Colorants and dyes
NEET Focus: Conceptually link structure → properties → applications.
| Topic | Key Points | NEET Focus |
|---|---|---|
| Ligands | Monodentate, bidentate, polydentate | Chelate stability, denticity |
| Coordination Number | 2, 4, 6 | Geometry prediction |
| Bonding | Werner’s theory, VBT, CFT | Color, magnetism, geometry |
| Isomerism | Structural & stereoisomerism | cis/trans, optical, ionization |
| Stability | Chelate effect, ligand nature | Industrial and biological relevance |
| Applications | Analytical, medicinal, industrial | NEET applied reasoning questions |
Coordination Chemistry is a crucial NEET Chemistry chapter. Conceptual understanding includes:
Ligand types, coordination number, and geometry
Bonding theories → VBT and CFT
Isomerism and stability
Applications in industry, medicine, and analytical chemistry
By linking structure → properties → applications, NEET aspirants can confidently tackle reasoning-based, application-oriented questions.
StudentBro.in provides structured, fully conceptual notes to help NEET aspirants master coordination chemistry efficiently, with H4 bold headings for readability and SEO optimization.