Q.CoSO4Cl⋅5NH3 exists in two isomeric forms 'A' and 'B'. Isomer 'A' reacts with AgNO3 to give white precipitate, but does not react with BaCl2. Isomer 'B' gives white precipitate with BaCl2 but does not react with AgNO3. Answer the following questions.
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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 & Ionisation Isomerism
Reasoning:
-
Analyse the precipitates:
AgNO3 tests for free Cl− ions (white AgCl precipitate). BaCl2 tests for free SO42− ions (white BaSO4 precipitate).
-
Interpret the data for A:
A gives AgCl with AgNO3 → Cl− is outside the coordination sphere.
A does not react with BaCl2 → SO42− is inside the coordination sphere.
So A is [Co(NH3)5SO4]Cl.
-
Interpret the data for B:
B gives BaSO4 with BaCl2 → SO42− is outside the sphere.
B does not react with AgNO3 → Cl− is inside the sphere.
So B is [Co(NH3)5Cl]SO4.
-
Isomerism type: …
The key idea is that the two isomers differ in which ions are free (outside the coordination sphere) and which are coordinated. Isomer A has free chloride (precipitates with AgNO3) but no free sulfate; isomer B has free sulfate (precipitates with BaCl2) but no free chloride. This is ionisation isomerism. The final identities are: A = [Co(NH3)5SO4]Cl and B = [Co(NH3)5Cl]SO4.
Why this approach works
In coordination compounds, the central metal ion and the ligands directly attached to it form the coordination sphere (written inside square brackets). Ions outside the sphere are free in solution and behave like simple ions — they can be detected by precipitation reactions.
AgNO3 tests for free chloride ions (Cl−), giving a white precipitate of AgCl.
BaCl2 tests for free sulfate ions (SO42−), giving a white precipitate of BaSO4.
So if an isomer gives a precipitate with one reagent but not the other, it tells us exactly which ion is outside the coordination sphere — and therefore which ion must be inside as a ligand.
Step-by-step reasoning
-
Write the molecular formula clearly
The compound is CoSO4Cl⋅5NH3. This means one cobalt, one sulfate, one chloride, and five ammonia molecules. Total charge: Co3+ (common oxidation state in such complexes), SO42−, Cl−, and 5NH3 (neutral) — so the complex is neutral overall.
-
Interpret the test results for isomer A
- A reacts with AgNO3 → white precipitate → free Cl− ions present.
- A does not react with BaCl2 → no free SO42− ions. Therefore, chloride is outside the coordination sphere, and sulfate must be inside as a ligand. Structure of A: [Co(NH3)5SO4]Cl
-
Interpret the test results for isomer B
- B gives white precipitate with BaCl2 → free SO42− ions present.
- B does not react with AgNO3 → no free Cl− ions. Therefore, sulfate is outside, and chloride must be inside as a ligand. Structure of B: [Co(NH3)5Cl]SO4
-
Identify the type of isomerism
Both isomers have the same molecular formula but differ in which anion is coordinated and which is free. This is ionisation isomerism — a type of structural isomerism where the isomers give different ions in solution. …
Method: Deductive Reasoning from Conductometric / Precipitation Data
This method uses the precipitation behaviour of the complex with specific reagents to determine which ions are free (outside the coordination sphere) and which are coordinated (inside the sphere).
Steps
Step 1: Identify the total composition
The formula is CoSO4Cl⋅5NH3.
- Cobalt(III) is the metal centre (common oxidation state +3 in ammine complexes).
- Ligands: 5 ammonia (NH3) molecules.
- Anionic species: one sulphate (SO42−) and one chloride (Cl−).
Step 2: Use precipitation tests to locate free ions
| Reagent | Precipitate with | Indicates free ion |
|---|---|---|
| AgNO3 | White precipitate (AgCl) | Free Cl− |
| BaCl2 | White precipitate (BaSO4) | Free SO42− |
-
Isomer A: reacts with AgNO3 → free Cl− present.
Does not react with BaCl2 → SO42− is coordinated (inside sphere).
-
Isomer B: reacts with BaCl2 → free SO42− present.
Does not react with AgNO3 → Cl− is coordinated (inside sphere).
Step 3: Write structural formulas
-
Isomer A:
Free Cl− outside, SO42− inside.
Coordination sphere: [Co(NH3)5SO4]+
Counter ion: Cl−
Formula: [Co(NH3)5SO4]Cl
-
Isomer B:
Free SO42− outside, Cl− inside. …
🚩 Common Mistakes & How to Avoid Them
1. Mistaking the formula as a simple double salt
- Mistake: Treating CoSO4Cl⋅5NH3 as a mixture of separate salts (like CoSO4 and CoCl2 with ammonia).
- Why it’s wrong: In coordination compounds, the dot (⋅) means the ammonia molecules are ligands attached to the central metal ion, not separate molecules.
- How to avoid: Always interpret MXn⋅yL as a complex where L are ligands coordinated to the metal M, and the anions (X) may be inside or outside the coordination sphere.
2. Confusing which ion is inside vs outside the coordination sphere
- Mistake: Assuming both SO42− and Cl− are outside the sphere.
- Why it’s wrong: The two isomers differ precisely because one anion is inside the coordination sphere and the other is outside.
- How to avoid: Use the precipitation tests as clues:
- AgNO3 gives white precipitate (AgCl) → free Cl− ions present.
- BaCl2 gives white precipitate (BaSO4) → free SO42− ions present.
- If a test gives no precipitate, that anion is inside the coordination sphere (not free).
3. Writing the wrong structural formula
- Mistake: Writing [Co(NH3)5Cl]SO4 for isomer A when it should be [Co(NH3)5SO4]Cl, or vice versa.
- How to avoid: Match the precipitation result:
- Isomer A reacts with AgNO3 → free Cl− → Cl is outside → formula: [Co(NH3)5SO4]Cl
- Isomer B reacts with BaCl2 → free SO42− → SO4 is outside → formula: [Co(NH3)5Cl]SO4
4. Naming the isomerism incorrectly
- Mistake: Calling it linkage isomerism or geometrical isomerism.
- Why it’s wrong: Linkage isomerism involves ambidentate ligands (like NO2− vs ONO−). Geometrical isomerism requires different spatial arrangements (cis/trans). Here, the difference is which anion is a ligand.
- How to avoid: Recognize that the two isomers have the same molecular formula but give different ions in solution — this is ionization isomerism.
5. Errors in IUPAC naming
- Mistake: Forgetting to name the anion outside the sphere correctly, or misordering ligands alphabetically.
- How to avoid: Follow IUPAC rules:
- Name ligands alphabetically (ignoring prefixes like penta-).
- Name the central metal with its oxidation state in Roman numerals.
- Name the counter ion (outside sphere) last.
- For sulfate as a ligand, use sulfato; for chloride as a ligand, use chlorido.
✓ Correct Solution
(i) Identify A and B with structural formulas
Isomer A (gives AgCl precipitate, no BaSO4):
- Free Cl− outside → SO42− is a ligand.
- Formula: [Co(NH3)5SO4]Cl
Isomer B (gives BaSO4 precipitate, no AgCl): …
- AP EAPCET 2026Set eng-2026-05-13-AN1 markMCQQ.Choose the correct formula for tris (ethane-1, 2-diamine) cobalt (III) hexacyanido ferrate (II) (A) [Co(en)3][Fe(CN)6] (B) [Co(en)3]2[Fe(CN)6]3 (C) [Co(en)3]3[Fe(CN)6]2 (D) [Co(en)3]4[Fe(CN)6]3
›Reveal solutionSolution
This tests naming-to-formula conversion for coordination compounds — figuring out ligand charges, metal oxidation states, and then balancing overall charge between cation and anion. The answer is [Co(en)3]4[Fe(CN)6]3.
Concept and Intuition
When a coordination compound's name specifies both a cationic complex and an anionic complex (as here — cobalt complex is the cation, ferrate complex is the anion), the overall salt must be electrically neutral. You find each complex ion's own charge first, then combine cation and anion in whatever whole-number ratio makes the total charge zero — exactly like balancing a simple ionic salt such as Al2O3 (from Al3+ and O2−).
Step-by-Step Solution
- Cation — tris(ethane-1,2-diamine)cobalt(III): "ethane-1,2-diamine" (en) is a neutral bidentate ligand (NH2CH2CH2NH2), and "tris" means three of them are attached: [Co(en)3]. The oxidation state of cobalt is given as (III), i.e. +3. Since en is neutral, the whole complex ion carries the metal's charge: [Co(en)3]3+.
- Anion — hexacyanidoferrate(II): "hexacyanido" means six CN− ligands, each carrying −1 charge, i.e. −6 total from ligands. "ferrate(II)" tells us iron is in the +2 state. Net charge of the complex ion =+2+(−6)=−4: [Fe(CN)6]4−. …
- AP EAPCET 2026Set ap-2026-05-19-AN1 markMCQQ.The IUPAC name of [PtCl2(H2N−CH2−CH2−NH2)2](NO3)2 is (A) Bis (ethane - 1,2 - diamine)dichloridoplatinum (IV) nitrate (B) Bis(ethane - 1,2 - diamine)dichloridoplatinum (IV) dinitrate (C) Dichloridobis (ethane - 1,2 - diamine)platinum (IV) nitrate (D) Dichloridobis(ethane - 1,2 - diamine)platinum (IV) dinitrate
›Reveal solutionSolution
This tests IUPAC coordination nomenclature: computing the metal's oxidation state and applying the alphabetical-ligand-order + no-prefix-on-a-Stock-named-counter-ion rules. Answer: Dichloridobis(ethane-1,2-diamine)platinum(IV) nitrate.
Concept and Intuition
A coordination compound name is built as [cationic complex or ligands][metal(oxidation state)] [anion]. Two separate rules govern it here: (1) ligands inside the complex are cited in alphabetical order by the ligand's own name, ignoring any multiplying prefix (mono/di/bis, tris...); (2) once the metal's oxidation state is stated in Roman numerals (Stock notation), the charge of the whole complex ion is fixed, so the number of counter-ions needed to balance it is implicit and is NOT restated with a multiplying prefix on the counter-ion's name.
Step-by-Step Solution
- Ligands: Cl− (chlorido, charge −1 each, two of them) and en = ethane-1,2-diamine (neutral, a bidentate ligand named with "bis" since its own name contains a numerical locant "1,2").
- Overall salt is [PtCl2(en)2](NO3)2, so the complex cation carries +2 charge (two nitrate anions balance it).
- Let Pt oxidation state be x: x+2(−1)+2(0)=+2⇒x=+4. So it's platinum(IV).
- Ligand naming: "chlorido" for Cl− ×2 → "dichlorido"; "ethane-1,2-diamine" ×2 → "bis(ethane-1,2-diamine)" (bis is used, not "di", because the ligand name itself already has numbers in it — using "di" would be ambiguous).
- Alphabetical citation order compares "chlorido" (c) vs "ethane-1,2-diamine" (e): c precedes e, so chlorido-containing part is written first: "Dichloridobis(ethane-1,2-diamine)platinum(IV)". …
- AP EAPCET 2025Set eng-2025-05-26-AN1 markMCQQ.The IUPAC name of the complex shown below is K3[Co(ox)3] (A) Tripotassium trioxalatocobaltate (III) (B) Potassium trioxalatecobaltate (III) (C) Potassium trioxalatecobalt (III) (D) Potassium trioxalatocobaltate (III)
›Reveal solutionSolution
IUPAC naming of coordination compounds: ligand 'oxalato' × 3 = 'trioxalato', anionic complex metal gets the '-ate' suffix ('cobaltate'), oxidation state by charge balance is +3, and the counter-cation 'potassium' is stated without a multiplying prefix — giving Potassium trioxalatocobaltate(III).
Concept and Intuition
Coordination-compound IUPAC names follow a fixed template: cation first, then ligands alphabetically with multiplying prefixes (bis/tris for complex ligand names, di/tri for simple ones like oxalato), then the metal name — with the special rule that if the complex ion is an anion, the metal name is modified to end in '-ate' (e.g. cobalt → cobaltate, iron → ferrate), followed by the oxidation state in Roman numerals in brackets.
Step-by-Step Solution
- Formula: K3[Co(ox)3], where 'ox' = oxalate ion (C2O42−), a bidentate ligand named 'oxalato' in coordination nomenclature.
- Charge balance: complex ion is [Co(ox)3]3− (balanced by 3 K+). Let Co oxidation state be x: x+3(−2)=−3⇒x=+3.
- Ligand prefix: three oxalato ligands → 'trioxalato' (using tri- since oxalato is a simple, unsubstituted ligand name).
- Since the complex ion is an anion, the metal name takes the anionic suffix: cobalt → 'cobaltate'.
- Combine: 'trioxalatocobaltate', with oxidation state (III) in brackets: 'trioxalatocobaltate(III)'. …
- AP EAPCET 2023Set eng-2023-05-16-FN1 markMCQQ.The formula of tris (ethane -1,2- diamine) cobalt (III) sulphate is: (A) [Co(H2NCH2CH2NH2)3]SO4 (B) [Co(H2NCH2CH2NH2)3]3(SO3)2 (C) [Co(CH3CH2NHNH2)3]2(SO4)3 (D) [Co(H2NCH2CH2NH2)3]2(SO4)3
›Reveal solutionSolution
The complex cation [Co(en)₃]³⁺ needs 2 cations for every 3 sulphate ions to balance charge, giving [Co(en)₃]₂(SO₄)₃.
Concept and Intuition
"Ethane-1,2-diamine" (en) is the neutral bidentate ligand H2NCH2CH2NH2. Cobalt(III) with three such neutral ligands gives a complex cation charge equal to the metal's oxidation state alone: [Co(en)3]3+. To form a neutral salt with sulphate (SO42−), the overall charges must balance using the smallest whole-number ratio — LCM of 3 and 2 is 6, so 2 cations (total +6) balance 3 sulphates (total −6).
Step-by-Step Solution
- Write the complex cation: [Co(H2NCH2CH2NH2)3]3+ (Co³⁺ + 3 neutral en ligands).
- Sulphate anion charge: SO42−.
- Balance charges: need ratio such that 2×3=3×2=6 → 2 cations : 3 sulphates. …
- AP EAPCET 2023Set eng-2023-05-17-AN1 markMCQQ.IUPAC name of [Pt(NH3)2Cl(NH2CH3)]Cl is (A) (Amino methane) chloro (diammine) platinum (II) chlolide (B) Chlorodiammine (methanamine) platinum (II) chloride (C) Diamminechloro (methanamine) platinum (II) chloride (D) Diamminechloro (methylamine) platinum (IV) chloride
›Reveal solutionSolution
Naming ligands alphabetically (ammine, chloro, methanamine) and computing Pt's oxidation state as +2 gives Diamminechloro(methanamine)platinum(II) chloride.
Concept and Intuition
IUPAC coordination nomenclature: (1) name ligands alphabetically using IUPAC ligand names (ignoring di/tri prefixes for alphabetization); (2) anionic ligands get '-o' suffix (chloro for Cl-); (3) metal oxidation state deduced from charge balance; (4) counter-ion named last.
Step-by-Step Solution
- Ligands in [Pt(NH3)2Cl(NH2CH3)]Cl: two NH3 (ammine, neutral), one Cl− (chloro, -1), one NH2CH3 = methanamine (neutral, the IUPAC ligand name for methylamine).
- Alphabetize ignoring 'di': ammine (a) < chloro (c) < methanamine (m) -> "diamminechloro(methanamine)". …
- AP EAPCET 2022Set eng-2022-07-05-FN1 markMCQQ.The homoleptic complex in the following is (A) [Co(NH3)4Br2]⊕ (B) [Co(C2O4)(NH3)4]⊕ (C) [Co(NH3)6]3⊕ (D) [Co(CN)4Cl2]⊖
›Reveal solutionSolution
A homoleptic complex has all identical ligands; only [Co(NH3)6]3+ qualifies among the given options.
Concept and Intuition
Coordination complexes are classified as homoleptic (all ligands of one single type bound to the metal) or heteroleptic (two or more different kinds of ligands). This is purely a matter of reading off the ligands present in each formula and checking whether they are all the same species.
Step-by-Step Solution
- [Co(NH3)4Br2]+ — ligands present: NH3 and Br− (two types) → heteroleptic.
- [Co(C2O4)(NH3)4]+ — ligands present: oxalate (C2O42−) and NH3 (two types) → heteroleptic.
- [Co(NH3)6]3+ — ligand present: only NH3, six of them → homoleptic. …
- AP EAPCET 2022Set eng-2022-07-07-FN1 markMCQQ.The IUPAC name of the following complex is [Co(NH2CH2CH2NH2)2Br2]Br (A) Bis (ethane-1, 2- diamine) dibromido cobalt (III) bromide (B) Di (ethane-1, 2- diamine) dibromido cobalt (III) bromide (C) Tribromido bis (ethane-1, 2- diamine) cobalt (III) (D) Dibromido bis (elthylene diamine) cobalt (III) bromide
›Reveal solutionSolution
The oxidation state of Co is +3 (from a +1 complex cation with two neutral en and two Br− ligands), and IUPAC alphabetical ligand ordering puts "bromido" before "(ethylenediamine)," giving dibromidobis(ethylenediamine)cobalt(III) bromide.
Concept and Intuition
Naming a coordination compound requires: (1) determining the metal's oxidation state from overall charge balance, (2) naming ligands with multiplying prefixes (di-, tri- for simple ligands; bis-, tris- for more complex/substituted ligand names like ethylenediamine, to avoid ambiguity), and (3) listing ligands in strict alphabetical order by ligand name (ignoring the multiplying prefix), followed by the metal name+oxidation state, then the counter-ion name.
Step-by-Step Solution
- The compound is [Co(en)2Br2]Br — one Br− is outside the coordination sphere (counter-ion), so the complex cation is [Co(en)2Br2]+.
- Charge balance inside the bracket: en is neutral (×2 = 0), Br− ligands contribute −2 (×2), so Co+0−2=+1⇒Co=+3.
- Ligand names: "ethylenediamine" (a bidentate amine, needs "bis" not "di" since its name itself could be ambiguous with a simple prefix) and "bromido" for Br−.
- Alphabetical order of ligand names (ignoring multiplying prefixes): "bromido" (b) before "ethylenediamine" (e). …
- AP EAPCET 2022Set eng-2022-07-08-AN1 markMCQQ.The IUPAC name of the following complex is [Cr(NH3)3(H2O)2Cl]Cl2 (A) Triamminediaqua chlorido chromium (III) chloride (B) Diaquatriammine chlorido chromium (III) chloride (C) Chlorido diaquatriammine chromium (III) chloride (D) Triammine diaqua trichlorido chromium (III)
›Reveal solutionSolution
Naming [Cr(NH3)3(H2O)2Cl]Cl2 requires listing ligands alphabetically (ammine, aqua, chlorido) with multiplying prefixes, then the oxidation state of Cr (found by charge balance) in Roman numerals, followed by the anion name — giving "triamminediaquachloridochromium(III) chloride".
Concept and Intuition
IUPAC naming of coordination compounds lists ligands in alphabetical order (by the first letter of the ligand name itself, ignoring multiplying prefixes like di-/tri-), followed by the name of the central metal with its oxidation state in Roman numerals in parentheses, and finally the counter-ion name (as a separate word) if the complex is a cation. The oxidation state of the metal is found by balancing charges: neutral ligands (NH₃, H₂O) contribute 0, anionic ligands contribute their charge, and the sum plus the metal's oxidation state must equal the overall charge of the complex ion.
Step-by-Step Solution
- Identify ligands inside the bracket: 3 NH₃ ("ammine" ×3 → "triammine"), 2 H₂O ("aqua" ×2 → "diaqua"), 1 Cl⁻ ("chlorido").
- Alphabetize by ligand name ignoring prefixes: compare "ammine", "aqua", "chlorido" — a-m-m... vs a-q-u-a: 'm' precedes 'q', so "ammine" comes before "aqua"; "chlorido" (starting with 'c') comes after both 'a' words. Order: ammine, aqua, chlorido.
- Combine with multiplying prefixes in that order: "triamminediaquachlorido".
- Determine oxidation state of Cr: the compound is neutral with 2 Cl⁻ as counter ions outside the bracket, so the complex ion charge is +2. Inside the bracket: 3(NH₃, 0) + 2(H₂O, 0) + 1(Cl⁻, −1) = −1. So Cr + (−1) = +2 → Cr = +3.
- Complete metal name: "chromium(III)". …
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