Q.When 1 mol CrCl3⋅6H2O is treated with excess of AgNO3, 3 mol of AgCl are obtained. The formula of the complex is:
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🔒 Start your 14-day free trial to unlock the full solution →Concept understanding — Coordination Compound Nomenclature
Coordination Compound Nomenclature: From Intuition to Precision
Imagine you're naming a person. You'd say "Ravi Sharma" — family name first, then given name. Coordination compounds have a similar logic, but the "family name" is the metal, and the "given names" are the groups attached to it. The rules are just a systematic way of writing that name so any chemist anywhere can draw the exact structure from it.
The Core Idea
A coordination compound has a central metal ion surrounded by molecules or ions called ligands. Think of the metal as the nucleus and ligands as planets orbiting it. The entire assembly (metal + ligands) is called the coordination sphere, and it's written inside square brackets: [Co(NH₃)₆]Cl₃.
The nomenclature rules tell you:
- What order to list things
- How to name each ligand
- How to indicate the metal's oxidation state
- How to handle the counter-ions outside the brackets
The Rules, Step by Step
1. Cation before anion (just like NaCl is sodium chloride)
If the complex ion is positive, it's named first. If it's negative, it's named last. Simple.
2. Within the coordination sphere: ligands first, then metal
This is the big rule. Ligands are named before the metal, in alphabetical order (ignoring prefixes like di-, tri-).
Alphabetical order is based on the ligand's name, not its formula. So NH₃ (ammine) comes before H₂O (aqua), even though N comes after H in the alphabet.
3. Naming ligands
| Ligand type | Name | Example |
|---|---|---|
| Neutral molecule (NH₃) | ammine | [Co(NH₃)₆]³⁺ → hexaamminecobalt(III) |
| Neutral molecule (H₂O) | aqua | [Cu(H₂O)₄]²⁺ → tetraaquacopper(II) |
| Neutral molecule (CO) | carbonyl | [Ni(CO)₄] → tetracarbonylnickel(0) |
| Negative ion (Cl⁻) | chloro | [PtCl₆]²⁻ → hexachloroplatinate(IV) |
| Negative ion (CN⁻) | cyano | [Fe(CN)₆]⁴⁻ → hexacyanoferrate(II) |
| Negative ion (OH⁻) | hydroxo | [Al(OH)₄]⁻ → tetrahydroxoaluminate(III) |
ammine (with two m's) is for NH₃ as a ligand. amine (one m) is for organic compounds like ethylamine. Don't mix them up — exam setters love this trap.
4. Prefixes for multiple ligands
Use Greek prefixes: di-, tri-, tetra-, penta-, hexa-, hepta-, octa-.
If the ligand name already contains a number (like ethylenediamine), use bis-, tris-, tetrakis- instead.
[Co(en)₃]³⁺ is tris(ethylenediamine)cobalt(III), not triethylenediaminecobalt(III). The parentheses around the ligand name are mandatory when using bis/tris/tetrakis.
5. Oxidation state of the metal
Write it in Roman numerals in parentheses right after the metal name. No space.
[Fe(CN)₆]³⁻ → hexacyanoferrate(III) (iron is in +3 state)
6. If the complex is an anion, change the metal's ending
| Metal | Anionic form |
|---|---|
| Cobalt | cobaltate |
| Copper | cuprate |
| Iron | ferrate |
| Nickel | nickelate |
| Platinum | platinate |
| Zinc | zincate |
General pattern:
[M(L)ₙ]Xₘ → cation name = [prefix-ligands]metal(oxidation state)
anion name = [prefix-ligands]metalate(oxidation state)
Worked Examples
Example 1: K₃[Fe(CN)₆]
- Cation: potassium (K⁺)
- Complex anion:
[Fe(CN)₆]³⁻ - Ligands: 6 cyano → hexacyano
- Metal: iron → ferrate (because it's an anion)
- Oxidation state: Fe is +3 (since 6 CN⁻ = -6, total charge -3, so Fe must be +3)
- Answer: Potassium hexacyanoferrate(III)
Example 2: [Co(NH₃)₅Cl]Cl₂
- Cation:
[Co(NH₃)₅Cl]²⁺ - Ligands: 5 ammine + 1 chloro → alphabetical: ammine before chloro → pentaamminechloro
- Metal: cobalt
- Oxidation state: Co is +3 (5 NH₃ neutral, 1 Cl⁻ = -1, total +2, so Co = +3) …
Why this formula?
Coordination Compound Nomenclature: Why the Rules Work
Coordination compound nomenclature isn't about a single formula — it's a system of rules built on a few core principles. Let's understand the why behind each major rule, so you never have to memorise blindly.
1. The Central Idea: Ligands as "Guests" Around a Metal "Host"
A coordination compound has a central metal atom/ion surrounded by ligands (molecules or ions that donate electron pairs). The naming reflects this relationship:
- Cation first, then anion (like normal ionic compounds)
- Ligands named before the metal (because they modify the metal's identity)
Why?
In chemistry, we name the more electropositive part first (cation). The metal-ligand complex is treated as a single unit — the ligands are "attached" to the metal, so they come first in the complex name.
2. Key Rule: Ligand Order — Alphabetical, Not by Charge
Rule: Ligands are named in alphabetical order (ignoring prefixes like di-, tri-).
Why?
- If we ordered by charge or size, the name would change every time a ligand is replaced.
- Alphabetical order is universal and unambiguous — it doesn't depend on the metal or oxidation state.
- Example:
[Co(NH₃)₄Cl₂]⁺is tetraamminedichlorocobalt(III) — "ammine" (a) before "chloro" (c).
3. Oxidation State: Why Roman Numerals?
Rule: The metal's oxidation state is written in Roman numerals in parentheses after the metal name.
Why?
- The oxidation state tells you the charge on the metal after accounting for ligand charges.
- Roman numerals avoid confusion with Arabic numbers (which are used for ligand counts).
- Example:
[Fe(CN)₆]³⁻→ hexacyanoferrate(III) — the iron is Fe³⁺, not Fe²⁺.
Derivation of oxidation state:
Let the complex charge = Q, ligand charges = sum of ligand charges L, number of ligands = n.
Then:
Metal oxidation state=Q−L
For [Fe(CN)₆]³⁻: CN⁻ has charge -1, so L=6×(−1)=−6, Q=−3.
Fe oxidation state=−3−(−6)=+3
4. Anionic Ligands: The "-o" Ending
Rule: Anionic ligands (negative ions) end in -o (e.g., Cl⁻ → chloro, CN⁻ → cyano, OH⁻ → hydroxo).
Why?
- This distinguishes them from neutral ligands (e.g., NH₃ → ammine, H₂O → aqua).
- The suffix -o signals "this ligand came from an anion" — crucial for charge balance.
Common examples:
| Anion | Ligand name |
|---|---|
| Cl⁻ | chloro |
| CN⁻ | cyano |
| OH⁻ | hydroxo |
| SO₄²⁻ | sulfato |
5. Neutral Ligands: Special Names
Rule: Neutral ligands keep their molecular name, except for a few with special names:
- NH₃ → ammine (not "ammonia")
- H₂O → aqua
- CO → carbonyl
- NO → nitrosyl
Why?
- "Ammine" avoids confusion with ammonia (NH₃) as a free molecule.
- These special names are historical but standardised — you must memorise them for exams.
6. Prefixes: di-, tri-, tetra-, etc.
Rule: Use Greek prefixes to indicate the number of each ligand:
- 2 → di, 3 → tri, 4 → tetra, 5 → penta, 6 → hexa
Why?
- Without prefixes,
[Co(NH₃)₆]³⁺would be "hexaamminecobalt(III)" — the "hexa" tells you there are six ammines. - For ligands with complex names (e.g., ethylenediamine), use bis-, tris-, tetrakis- to avoid confusion.
Example:
[Co(en)₃]³⁺ → tris(ethylenediamine)cobalt(III) — "tris" because "triethylenediamine" would sound like three ethylenediamine molecules (which is correct, but "tris" is clearer).
7. Anionic Complexes: The "-ate" Suffix …
Concept: Coordination Compound Nomenclature — the number of AgCl moles precipitated equals the number of chloride ions present outside the coordination sphere (i.e., free or ionizable Cl−).
Reasoning:
- Excess AgNO3 precipitates only the chloride ions that are not coordinated to the metal centre.
- 3 mol of AgCl means 3 mol of free Cl− per mole of complex. …
The key is that only chloride ions outside the coordination sphere (counter ions) precipitate with AgNO3. Since 3 mol of AgCl form per mol of complex, all three chlorides are counter ions, so the formula must be [Cr(H2O)6]Cl3 — option (iv).
This problem tests your understanding of coordination compound nomenclature and the difference between coordination sphere and counter ions. When you treat a complex with AgNO3, the silver ions only precipitate chloride ions that are free — those outside the square brackets. Chloride ions inside the coordination sphere (bonded directly to the metal) do not dissociate and will not react with Ag+.
The question gives you a critical experimental fact: 1 mol of the complex yields 3 mol of AgCl. That means all three chloride ions present in the formula unit are outside the coordination sphere. None are bonded to chromium.
Let’s check each option systematically.
-
Option (i): [CrCl3(H2O)3]⋅3H2O
Here, all three chlorides are inside the coordination sphere. The three water molecules outside are just water of crystallization. So zero free Cl− ions — this would give 0 mol of AgCl. Eliminated.
-
Option (ii): [CrCl2(H2O)4]Cl⋅2H2O
Two chlorides are inside the sphere, one is outside as a counter ion. So only 1 mol of AgCl would precipitate. Not matching the given 3 mol. Eliminated.
-
Option (iii): [CrCl(H2O)5]Cl2⋅H2O
One chloride inside, two outside. That gives 2 mol of AgCl. Still not enough. Eliminated.
-
Option (iv): [Cr(H2O)6]Cl3 …
Method: Conductometric / Precipitation Analysis of Ionizable Chloride
This method uses the fact that only free (ionizable) chloride ions outside the coordination sphere react with AgNO3 to give AgCl precipitate. Chloride ions inside the coordination sphere (ligands) do not precipitate.
Steps
Step 1: Identify the given data
- 1 mol of complex → 3 mol of AgCl
- This means 3 mol of free Cl− are present per mol of complex.
Step 2: Count total chloride in each option
All options have total 3 Cl atoms per formula unit. But only those outside the square bracket are free.
Step 3: Check each option for number of free Cl−
-
(i) [CrCl3(H2O)3]⋅3H2O
→ All 3 Cl are inside coordination sphere → 0 free Cl → gives 0 mol AgCl ✗
-
(ii) [CrCl2(H2O)4]Cl⋅2H2O …
Common Mistakes & How to Avoid Them
Mistake 1: Confusing total chloride with ionizable chloride
The error: Students see 3 mol of AgCl formed and assume the complex contains 3 chloride ions in the coordination sphere — picking option (i) or (iv) without thinking.
Why it's wrong: AgNO₃ only precipitates free chloride ions (outside the coordination sphere). Chloride ions inside the coordination sphere (bonded to Cr) do not react with Ag⁺.
How to avoid: Always ask: "Which Cl⁻ are free to precipitate?" Only the counter ions (outside square brackets) react with AgNO₃.
Mistake 2: Forgetting water can be inside or outside the coordination sphere
The error: Students count all 6 water molecules as hydrate water (outside brackets) or all as coordinated water (inside brackets), ignoring that water can be both.
Why it's wrong: The formula CrCl3⋅6H2O tells total composition — it doesn't show how water is distributed. Some water may be coordinated to Cr, some may be outside as water of crystallization.
How to avoid: Remember: water molecules can be inside the coordination sphere (ligands) or outside (lattice water). The dot (⋅) separates the complex from crystallization water.
Mistake 3: Not balancing charge and coordination number
The error: Picking an option without checking if Cr's coordination number (usually 6) and oxidation state are consistent.
Why it's wrong: Cr³⁺ typically has coordination number 6. Each option must have exactly 6 ligands (Cl⁻ + H₂O) in the coordination sphere.
How to avoid: For each option:
- Count total ligands inside brackets = must be 6
- Check charge balance: Cr³⁺ + (ligand charges) + (counter ion charges) = 0
Mistake 4: Rushing to pick the first option that "looks right"
The error: Seeing 3 mol AgCl and immediately choosing option (iv) [Cr(H2O)6]Cl3 because it has 3 Cl⁻ outside.
Why it's wrong: Option (iv) gives 3 mol AgCl — but so does option (iii)! Both have 3 ionizable Cl⁻. You must check all conditions.
How to avoid: Test every option systematically: …
- Higher Secondary (+2 Stage) Examination 2025Set ANNUAL1 markQ.Write the IUPAC formula of the complex compound pentaamminenitrito-O-cobalt(III) chloride.
›Reveal solutionSolution
'Pentaammine' gives 5 NH3 ligands, 'nitrito-O' gives the nitrite ion bonded through its oxygen (ONO-), and 'cobalt(III)' fixes the metal's oxidation state at +3, needing 2 Cl- as counter ions.
Step 1 - decode the name. 'Pentaammine' = five NH3 (neutral) ligands. 'Nitrito-O' = the nitrite ligand (NO2-) coordinated through its oxygen atom, written as -ONO (as opposed to 'nitrito-N' which would coordinate through nitrogen, written as -NO2). 'Cobalt(III)' = the central metal is Co in the +3 oxidation state.
…
- Higher Secondary (+2 Stage) Examination 2024Set ANNUAL1 markQ.Write the IUPAC name of the compound K3[Fe(C2O4)3].
›Reveal solutionSolution
Naming K3[Fe(C2O4)3]: the cation (potassium) is named first, then the anionic complex, with oxalate (bidentate, named "oxalato") counted using "tris" (rather than "tri") since it is itself a compound ligand name, ending in "-ate" with the metal's oxidation state in Roman numerals because the complex ion is anionic.
Working out Fe's oxidation state: overall charge on 3K+ is +3, so the complex ion [Fe(C2O4)3] must be 3– overall. Oxalate (C2O4^2-) contributes 3 × (–2) = –6.
x + (–6) = –3 → x = +3
So iron is in the +3 oxidation state.
…
- Higher Secondary (+2 Stage) Examination 2023Set ANNUAL1 markQ.Write the IUPAC name of Na3[Co(NO2)6].
›Reveal solutionSolution
Na3[Co(NO2)6] is an anionic complex; naming it requires the ligand name (nitrito), the metal name with an "-ate" ending, and the oxidation state of cobalt (determined from charge balance) in Roman numerals.
Working out the oxidation state of Co: the complex ion is [Co(NO2)6]^3- (charge balances 3 Na+). Each nitrito ligand, NO2-, carries a charge of -1; with 6 of them: 6 x (-1) = -6. Let the oxidation state of Co be x:
x + (-6) = -3 (overall charge of the complex ion)
x = +3
So cobalt is in the +3 oxidation state.
Naming rules for an anionic complex:
- ligands are named in alphabetical order with a multiplying prefix (nitrito x 6 = hexanitrito)
- since the complex is an ANION, the metal name takes the suffix "-ate": cobalt -> cobaltate …
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