Coordination Compounds is the top-scoring inorganic chapter of Class 12. This Collegedunia formula sheet puts every nomenclature rule, CFSE table, and hybridisation cue on one revision page, fully retained in the 2026-27 NCERT.

  • CBSE Weightage: 7 to 8 marks
  • JEE Main Weightage: 4 to 6 percent (3 to 4 questions per paper)
  • NEET Weightage: 3 to 4 questions per year
26 Formulae & Relations | 2026-27 NCERT Edition

Curated by subject experts and mapped to the 2026-27 NCERT edition.

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Coordination Compounds Formula Sheet - Class 12 Chemistry
Spin-Only Magnetic Moment Formula for Coordination Compounds

Coordination Compounds Class 12 Chemistry Explained

Source: Magnet Brains on YouTube

Coordination Compounds Symbol Glossary for Class 12 Chemistry

The glossary below locks in every notation used in the master table.

SymbolMeaningTypical Unit / Value
MCentral metal atom or ion-
LGeneric ligand (neutral or charged)-
CNCoordination number (secondary valency)integer, usually 4 or 6
OSOxidation state of M (primary valency)integer, often +2 / +3
ΔoOctahedral crystal field splittingkJ mol-1 or cm-1
ΔtTetrahedral crystal field splittingkJ mol-1
PElectron pairing energykJ mol-1
nNumber of unpaired electrons in d-orbital of Mn+dimensionless
μSpin-only magnetic momentBohr Magneton (BM)
EANEffective atomic numberdimensionless

Coordination Compounds All Important Formulae for Class 12 Chemistry

The master table lists every formula and relation in NCERT Chapter 5, with units, section, and exam cue. All entries are retained in 2026-27.

ConceptFormula / RelationValue or UnitNCERT RefCommon Use
Werner's primary valencyEquals OS of M, satisfied by negative ions-5.1Identify counter ion
Werner's secondary valencyEquals CN of M, satisfied by ligands-5.1Identify ligand count
Coordination sphere notation [M(L)n]q q = net charge5.2Bracket convention
OS of central metal OS(M) = q - ∑ (charge of each L) integer5.3Compute from formula
EAN rule EAN = Z(M) - OS(M) + 2 × CN dimensionless5.5Stability of complex
Spin-only magnetic moment μ = n(n+2) BM5.7From n unpaired e-
μ for n = 1 μ = 1.73 BM5.7d1, d9 low spin
μ for n = 2 μ = 2.83 BM5.7d2, d8 octahedral
μ for n = 3 μ = 3.87 BM5.7d3, d7 low spin
μ for n = 4 μ = 4.90 BM5.7d4, d6 high spin (oct)
μ for n = 5 μ = 5.92 BM5.7d5 high spin (Fe3+, Mn2+)
Tetrahedral vs octahedral splitting t = 49o ≈ 0.45 o kJ mol-15.7Why tet is always high spin
CFSE (octahedral) CFSE = [-0.4 n(t2g) + 0.6 n(eg)] o + xP kJ mol-15.7Stability + spin state
CFSE (tetrahedral) CFSE = [-0.6 n(e) + 0.4 n(t2)] t kJ mol-15.7Always high spin
Low-spin condition o > P -5.7Strong-field ligand
High-spin condition o < P -5.7Weak-field ligand
Spectrochemical series (key cues) I- < Br- < Cl- < F- < OH- < H2O < NH3 < en < NO2- < CN- < CO -5.7Rank Δo
Stability constant (overall) n = [MLn][M][L]n varies5.6Compare complex stability
Stepwise stability Kn = [MLn][MLn-1][L] varies5.6K1 > K2 > ... typical
Geometrical isomerism (CN 6) [Ma4b2] → cis, trans -5.42 isomers
Geometrical isomerism (CN 6) [Ma3b3] → fac, mer -5.42 isomers
Optical isomerism [M(en)3]n+ → Δ, Λ -5.4Chelate octahedral
Linkage isomerismNO2- vs ONO-; SCN- vs NCS--5.4Ambidentate ligand
Wavelength of d-d transition o = hcλ J per ion5.7Colour of complex
Hybridisation (CN 4 sq planar) dsp2 (inner) or sp2d -5.7d8 low spin (Ni2+, Pt2+)
Hybridisation (CN 4 tetrahedral) sp3 -5.7NiCl42-, [Ni(CO)4]
Hybridisation (CN 6) d2sp3 (inner) or sp3d2 (outer)-5.7Low spin vs high spin

CFSE shortcut: write the d-electron count, fill t2g and eg from the spectrochemical cue, then plug into the formula. Forgetting the +xP correction is the most common 1-mark slip in CFSE numericals.

How will Collegedunia's Coordination Compounds Formula Sheet Help You?

Built for a 30-minute last-pass revision before any Chemistry paper.

  • 2026-27 NCERT Alignment: Matches Sections 5.1 to 5.8 of the current print.
  • One-Page Printability: The master table fits one A4 landscape sheet.
  • Field Tagging: Each ligand is tagged strong or weak so CFSE direction is instant.
  • Expert Verification: Cross-checked against the last five JEE Main and NEET papers.

Why the Coordination Compounds Formula Sheet is a Top-Yield Asset for Class 12th Boards and Entrances

CBSE carries at least one 5-mark long-answer on this chapter in every board paper since 2019. JEE Main rotates two to four CFSE, hybridisation, or isomer MCQs per paper, and NEET asks one EAN or magnetic-moment question every year.

Watch Out: In a coordination compound formula, metal comes first, then ligands in alphabetical order ignoring prefixes (di, tri, bis). Anionic ligands take an -o suffix (Cl → chlorido). Mixing formula order with name order is a common 1-mark slip.
Crystal Field Stabilisation Energy (CFSE) Formula and Pairing Energy

When to Use Which Formula in Coordination Compounds

Match the question stem to the formula.

  • "Find OS of M in [M(L)n]q": OS = q - sum of ligand charges. Neutral ligands contribute 0.
  • "Compute EAN": EAN = Z(M) - OS(M) + 2 x CN. Compare with nearest noble-gas number.
  • "Calculate μ": read spin state from the ligand field, count unpaired d-electrons, apply μ = n(n+2) BM.
  • "Predict hybridisation": CN 4 weak → sp3; CN 4 strong d8 → dsp2; CN 6 strong → d2sp3; CN 6 weak → sp3d2.
  • "Count isomers": apply the geometrical-isomer rules and check optical activity in chelated octahedrals.

Coordination Compounds CFSE Configuration Reference Table

These CFSE rows cover almost every numerical asked since 2021. Use them as the lookup table while solving.

d-electron countFieldt2g, eg fillingCFSEUnpaired e-
d4Weak (high spin)t2g3 eg1-0.6 Δo4
d4Strong (low spin)t2g4 eg0-1.6 Δo + P2
d5Weak (high spin)t2g3 eg205
d5Strong (low spin)t2g5 eg0-2.0 Δo + 2P1
d6Weak (high spin)t2g4 eg2-0.4 Δo4
d6Strong (low spin)t2g6 eg0-2.4 Δo + 2P0
d7Weak (high spin)t2g5 eg2-0.8 Δo3
d7Strong (low spin)t2g6 eg1-1.8 Δo + P1
Quick Tip: d5 high spin gives CFSE = 0, so Mn2+ and Fe3+ aqua complexes are pale.

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In a Collegedunia poll of 900 Class 12 students, 78% said the one-page CFSE and hybridisation table cut their Coordination Compounds revision time before boards.

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Coordination Compounds Class 12 Chemistry Formula Sheet FAQs

Ques. Where can I download the Coordination Compounds Class 12 Chemistry Formula Sheet PDF?

Ans. You can download the Coordination Compounds Class 12 Chemistry Formula Sheet PDF directly from this Collegedunia page. Both the Normal and HD versions are available and free.

Ques. Is this Formula Sheet aligned with the 2026-27 NCERT?

Ans. Yes. This page reflects the current 2026-27 syllabus for Class 12 Chemistry. The Coordination Compounds chapter is fully retained in the new edition with no formula cuts; every relation in Sections 5.1 to 5.8 of the NCERT remains examinable.

Ques. How many pages is the Class 12th Chemistry Coordination Compounds Formula Sheet PDF?

Ans. The Formula Sheet PDF runs approximately 8 pages and covers the master formula table, symbol glossary, CFSE configuration reference, quick-fact MCQ cards, when-to-use decision tree, and four common numerical pattern templates.

Ques. What is the formula for CFSE in an octahedral complex?

Ans. The crystal field stabilisation energy of an octahedral complex is CFSE = [-0.4 n(t2g) + 0.6 n(eg)] Δo + xP, where n(t2g) and n(eg) are the electrons in the lower and higher d-orbital sets and xP is the energy cost of x extra electron pairs formed (relative to the free ion).

Ques. How do I compute the EAN of a coordination complex?

Ans. EAN (Effective Atomic Number) = Z(M) - OS(M) + 2 x CN, where Z(M) is the atomic number of the central metal, OS is its oxidation state, and CN is the coordination number. For [Ni(CO)4], EAN = 28 - 0 + 8 = 36 (Kr config), justifying the high stability.

Ques. Why is Δt always less than Δo?

Ans. For the same metal, ligands and bond distances, Δt = (4/9) Δo ≈ 0.45 Δo. Tetrahedral geometry has only 4 ligands (vs 6) and none of them sits directly along the d-orbital lobes, so the splitting is smaller. Consequently Δt never exceeds the pairing energy P, and tetrahedral complexes are always high spin.

Ques. How do I rank ligands using the spectrochemical series?

Ans. The series ranks ligands by the Δo they produce: I- < Br- < Cl- < F- < OH- < H2O < NH3 < en < NO2- < CN- < CO. Strong-field ligands at the right end (CN-, CO, en, NO2-) drive low-spin configurations; weak-field ligands at the left end (halides, water) keep complexes high spin.

Ques. What types of isomerism are shown by coordination compounds?

Ans. Coordination compounds show structural isomerism (ionisation, hydrate, linkage, coordination) and stereoisomerism (geometrical cis-trans and fac-mer, optical Δ / Λ). [Co(NH3)4Cl2]+ shows cis-trans; [Co(en)3]3+ shows optical activity; NO2- vs ONO- gives linkage isomers.

Ques. What is the spin-only magnetic moment formula for coordination compounds?

Ans. The spin-only magnetic moment is μ = n(n+2) BM, where n is the number of unpaired d-electrons in the metal ion after considering the ligand field. Quick values: n = 1 gives 1.73 BM, n = 2 gives 2.83 BM, n = 3 gives 3.87 BM, n = 4 gives 4.90 BM, n = 5 gives 5.92 BM. Always classify the ligand as strong or weak field first, then count unpaired electrons.

Ques. What is the difference between primary valence and secondary valence in Werner's theory?

Ans. Primary valence equals the oxidation state of the central metal, is ionisable, and is satisfied by anions outside the coordination sphere. Secondary valence equals the coordination number, is non-ionisable, satisfied by ligands inside the sphere, and is directional - it fixes the geometry. In [Co(NH3)5Cl]Cl2, Co3+ has primary valence 3 and secondary valence 6.

Ques. What is the chelate effect and why does it stabilise complexes?

Ans. The chelate effect is the extra thermodynamic stability of complexes formed by polydentate (chelating) ligands compared to monodentate-only analogues. The driver is entropy: replacing two monodentate ligands with one bidentate ligand releases free water molecules into the bulk, raising disorder. [Ni(en)3]2+ is about 105 times more stable than [Ni(NH3)6]2+; EDTA4- sequesters Pb2+ and Hg2+ in heavy-metal therapy through five chelate rings.

Ques. What is the synergic effect in metal carbonyls like Ni(CO)4?

Ans. Metal carbonyls have a two-way bond. The C lone pair of CO donates into an empty metal hybrid orbital ( σ donation), and a filled metal d-orbital donates back into the empty π* anti-bonding orbital of CO ( π back-bonding). Back-donation strengthens the M-C bond and weakens the C-O bond, dropping the C-O stretching frequency from 2143 cm-1 in free CO to roughly 2050 cm-1 in Ni(CO)4. Ni(CO)4 uses sp3 hybridisation, is tetrahedral and diamagnetic, with EAN = 36.

Ques. Which coordination compounds appear in biology - haemoglobin, chlorophyll, Vitamin B12?

Ans. Haemoglobin is an Fe2+-porphyrin complex that binds O2 reversibly. Chlorophyll is the Mg2+-porphyrin (chlorin) that drives photosynthesis. Vitamin B12 (cyanocobalamin) is a Co3+-corrin complex with CN- as the sixth ligand. Cisplatin (cis-[Pt(NH3)2Cl2]) is the platinum anticancer drug; only the cis isomer cross-links with DNA. EDTA chelates lead and mercury in heavy-metal therapy.