CUET UG Chemistry Booster Test - 3 Nomenclature
📌 Answers are locked once submitted — results and explanations appear at the end.
QUESTION 1 OF 20
Why is the additive nomenclature system exceptionally vital for compounds like [CoCl₂(NH₃)₄]⁺?
QUESTION 2 OF 20
Evaluate the following rules from the 2004 IUPAC draft regarding nomenclature. Choose the correct statements:
1. Ligands are sorted alphabetically irrespective of their charge.
2. Anionic ligands must end in -ido.
3. The central atom is always named before the ligands.
4. Neutral complexes are named similarly to complex cations.
QUESTION 3 OF 20
Deduce the correct sequence of components to write the chemical formula for potassium trioxalatoaluminate(III):
1. K
2. [Al
3. ₃
4. (C₂O₄)₃]
QUESTION 4 OF 20
In the coordination formula [Co(NH₃)₅(CO₃)]Cl, why is the carbonate group enclosed in parentheses while the ammine group is as well, but chloride is not?
QUESTION 5 OF 20
Match the abbreviated ligand (List-I) with the letter used to determine its alphabetical position in a chemical formula (List-II):
| List I | List II |
|---|---|
| 1. en (ethane-1,2-diamine) | a. e |
| 2. EDTA | b. p |
| 3. ox (oxalate) | c. o |
| 4. py (pyridine) | d. E |
QUESTION 6 OF 20
A complex contains one chloride ion, one nitrite ion, and four ammine molecules attached to Cobalt(III). Assuming formula writing rules (alphabetical listing irrespective of charge), which represents the correct formula?
QUESTION 7 OF 20
In the complex [Cr(NH₃)₃(H₂O)₃]Cl₃, the numerical "unit" multiplier for the ammine ligands in its IUPAC name is represented by:
QUESTION 8 OF 20
Determine the correct IUPAC name for [CoCl₂(en)₂]⁺:
QUESTION 9 OF 20
The distinction between naming a ligand "nitrito-N" versus "nitrito-O" identifies what type of specific ligand behavior?
QUESTION 10 OF 20
When forming the name of [Co(NH₃)₅(H₂O)]³⁺, which correctly reflects the naming rules for neutral ligands?
QUESTION 11 OF 20
In the linkage isomer [Co(NH₃)₅(NO₂)]Cl₂, the complex entity is a cation. How must the central metal be formally named?
QUESTION 12 OF 20
In the nomenclature of Hg[Co(SCN)₄], the central metal of the complex anion is named:
QUESTION 13 OF 20
The Roman numeral placed in parentheses after the metal's name defines:
QUESTION 14 OF 20
Determine the oxidation state of the central metal in the complex [Pt(NH₃)(H₂O)Cl₂]:
QUESTION 15 OF 20
The complex [Ni(H₂O)₆]²⁺ is formed when nickel(II) chloride is dissolved in water. By IUPAC rules, this complex is categorized as a:
QUESTION 16 OF 20
In the coordination isomer [Co(NH₃)₆][Cr(CN)₆], the [Cr(CN)₆]³⁻ entity represents:
QUESTION 17 OF 20
For the compound [Cr(NH₃)₃(H₂O)₃]Cl₃, how is electrical neutrality achieved in the written formula?
QUESTION 18 OF 20
Which formatting rule prevents ambiguity when defining the exact boundaries of the primary and secondary valences in a written chemical formula?
QUESTION 19 OF 20
Based on the passage's explanation, why is 'ammine' placed before 'aqua' in the name triamminetriaquachromium(III) chloride?
QUESTION 20 OF 20
According to the passage, how is the oxidation number of the chromium metal (+3) deduced from the formula [Cr(NH₃)₃(H₂O)₃]Cl₃?
Test Complete!
Answer Review
1 Why is the additive nomenclature system exceptionally vital for compounds like [CoCl₂(NH₃)₄]⁺?
�� Additive nomenclature provides systematic naming. �� It distinguishes coordination isomers and stereoisomers. �� Cis and trans forms require unique identification.
Additive nomenclature was developed to provide an unambiguous naming system for coordination compounds. Complexes such as [CoCl₂(NH₃)₄]⁺ can exist as cis and trans isomers that possess the same empirical formula but differ in spatial arrangement. The nomenclature system explicitly identifies these differences through appropriate descriptors, ensuring that each distinct structure receives a unique name. Therefore, the major importance of additive nomenclature is its ability to distinguish structural and stereochemical variations systematically.
- �� Option A → Solubility depends on intermolecular interactions and is not determined by nomenclature.
- �� Option C → Nomenclature does not alter the primary valence or oxidation state of a metal.
- �� Option D → Oxidation state determination remains an essential part of coordination compound nomenclature.
Used
- Definition Matching
Application:
- �� Identify the primary purpose of additive nomenclature in coordination chemistry.
Final Logic:
- �� Additive nomenclature uniquely identifies isomers having the same molecular formula.
- Same Formula, Different Shape → Need Different Name
2 Evaluate the following rules from the 2004 IUPAC draft regarding nomenclature. Choose the correct statements:
1. Ligands are sorted alphabetically irrespective of their charge.
2. Anionic ligands must end in -ido.
3. The central atom is always named before the ligands.
4. Neutral complexes are named similarly to complex cations.
�� Ligands are arranged alphabetically. �� Anionic ligands generally end with "-ido". �� Metal name comes after ligand names.
Evaluate each statement: • Statement 1 → Correct. Ligands are arranged alphabetically irrespective of their charge. • Statement 2 → Correct. Modern IUPAC nomenclature uses the suffix "-ido" for anionic ligands. • Statement 3 → Incorrect. Ligands are named before the central metal atom. • Statement 4 → Correct. Neutral complexes are named in the same manner as cationic complexes. Hence Statements 1, 2 and 4 are correct.
- �� Option A → Includes Statement 3, which is incorrect.
- �� Option C → Omits Statements 1 and 2, which are correct.
- �� Option D → Includes Statement 3, which is incorrect and omits Statement 1.
Used
- Elimination
Application:
- �� Check each statement against IUPAC naming rules.
Final Logic:
- �� Statements 1, 2 and 4 are correct while Statement 3 violates the ligand-before-metal rule.
- Ligands First, Metal Last
3 Deduce the correct sequence of components to write the chemical formula for potassium trioxalatoaluminate(III):
1. K
2. [Al
3. ₃
4. (C₂O₄)₃]
�� Potassium is the counter cation. �� Three K⁺ ions balance the complex anion. �� Formula becomes K₃[Al(C₂O₄)₃].
The complex anion is: [Al(C₂O₄)₃]³⁻ To neutralize the −3 charge, three K⁺ ions are required: K₃[Al(C₂O₄)₃] Thus the sequence is: • 1 → K • 3 → ₃ • 2 → [Al • 4 → (C₂O₄)₃] Therefore the correct order is: 1, 3, 2, 4
- �� Option B → Places the coordination entity before the counter ion.
- �� Option C → Places the subscript after the complex.
- �� Option D → Produces an incorrect formula arrangement.
Used
- Substitution
Application:
- �� Construct the actual chemical formula from the compound name.
Final Logic:
- �� Potassium trioxalatoaluminate(III) = K₃[Al(C₂O₄)₃].
- Counter Ion First, Complex Next
4 In the coordination formula [Co(NH₃)₅(CO₃)]Cl, why is the carbonate group enclosed in parentheses while the ammine group is as well, but chloride is not?
�� Ligands within the coordination sphere are enclosed appropriately. �� Carbonate and ammine are coordinated ligands. �� Chloride acts as a counter ion.
Within the coordination sphere, ligands are attached directly to the central metal ion. Carbonate (CO₃²⁻) and ammine (NH₃) function as ligands and are represented within the coordination entity. Chloride is outside the coordination sphere and acts as a counter ion. Therefore, it is not enclosed as part of the ligand notation.
- �� Option B → Ligand charge is not the reason for bracket placement.
- �� Option C → Parentheses do not indicate oxidation state.
- �� Option D → Parentheses are not restricted to anions.
Used
- Definition Matching
Application:
- �� Identify the role of each species in the coordination compound.
Final Logic:
- �� Coordinated ligands are written inside the coordination sphere, counter ions outside.
- Inside = Ligand, Outside = Counter Ion
5 Match the abbreviated ligand (List-I) with the letter used to determine its alphabetical position in a chemical formula (List-II):
| List I | List II |
|---|---|
| 1. en (ethane-1,2-diamine) | a. e |
| 2. EDTA | b. p |
| 3. ox (oxalate) | c. o |
| 4. py (pyridine) | d. E |
�� Alphabetization uses ligand abbreviations. �� en begins with e. �� EDTA begins with E, ox with o, py with p.
Matching: • 1 → a (en → e) • 2 → d (EDTA → E) • 3 → c (ox → o) • 4 → b (py → p) Hence the correct matching is: 1-a, 2-d, 3-c, 4-b.
- �� Option B → Incorrectly assigns EDTA and en.
- �� Option C → Multiple alphabetical mismatches.
- �� Option D → Incorrect assignments for EDTA and oxalate.
Used
- Definition Matching
Application:
- �� Match each ligand abbreviation with its alphabetical starting letter.
Final Logic:
- �� Alphabetization follows the ligand abbreviation itself.
- en-e, EDTA-E, ox-o, py-p
6 A complex contains one chloride ion, one nitrite ion, and four ammine molecules attached to Cobalt(III). Assuming formula writing rules (alphabetical listing irrespective of charge), which represents the correct formula?
�� Ligands are arranged alphabetically. �� Ammine comes before chlorido and nitrito. �� Charge does not affect ordering.
Alphabetical order: ammine (A) chlorido (C) nitrito (N) Thus the correct ligand arrangement is: [Co(NH₃)₄Cl(NO₂)]⁺ Therefore Option B follows IUPAC formula-writing rules.
- �� Option A → Chlorido incorrectly precedes ammine.
- �� Option C → Nitrito incorrectly appears first.
- �� Option D → Nitrito incorrectly precedes chlorido.
Used
- Option Grouping
Application:
- �� Arrange ligands according to alphabetical order.
Final Logic:
- �� Ammine → Chlorido → Nitrito.
- A before C before N
7 In the complex [Cr(NH₃)₃(H₂O)₃]Cl₃, the numerical "unit" multiplier for the ammine ligands in its IUPAC name is represented by:
�� Three identical simple ligands are present. �� Simple ligands use mono, di, tri, tetra. �� Ammine is a simple ligand.
NH₃ is a simple ligand. When three such ligands are present, the numerical prefix used is "tri". Hence the name contains triammine. Prefixes like bis, tris and tetrakis are reserved for more complex ligand names.
- �� Option A → Tris is used for complex ligand names.
- �� Option C → IUPAC uses prefixes, not ordinary numbers.
- �� Option D → Indicates four ligands.
Used
- Definition Matching
Application:
- �� Identify the appropriate multiplicative prefix.
Final Logic:
- �� Three simple ligands = tri.
- 3 Simple Ligands = Tri
8 Determine the correct IUPAC name for [CoCl₂(en)₂]⁺:
�� Two chlorido ligands → dichlorido. �� Two ethane-1,2-diamine ligands → bis. �� Complex is cationic → cobalt(III).
The ligands present are: 2 chlorido ligands → dichlorido 2 ethane-1,2-diamine ligands → bis(ethane-1,2-diamine) Since the complex is cationic, the metal name remains cobalt(III). Therefore the correct name is Dichloridobis(ethane-1,2-diamine)cobalt(III).
- �� Option B → Incorrect use of cobaltate and ligand naming.
- �� Option C → Violates ligand alphabetical order.
- �� Option D → Uses tris despite only two en ligands.
Used
- Rule Application
Application:
- �� Apply ligand naming, prefixes and metal naming rules.
Final Logic:
- �� Dichlorido + bis(en) + cobalt(III).
- Complex Ligand Repeated Twice = Bis
9 The distinction between naming a ligand "nitrito-N" versus "nitrito-O" identifies what type of specific ligand behavior?
�� Nitrite can coordinate through N or O. �� Different donor atoms produce linkage isomers. �� Such ligands are ambidentate.
The nitrite ion (NO₂⁻) can coordinate through either nitrogen or oxygen. When the same ligand binds through different donor atoms, linkage isomerism arises. Such ligands are called ambidentate ligands. Therefore nitrito-N and nitrito-O represent ambidentate linkage behavior.
- �� Option A → Chelation involves multiple donor atoms simultaneously.
- �� Option C → Optical isomerism involves non-superimposable mirror images.
- �� Option D → Hydrate formation is unrelated.
Used
- Definition Matching
Application:
- �� Identify the coordination behavior described.
Final Logic:
- �� Same ligand, different donor atom = ambidentate linkage.
- One Ligand, Two Attachment Points
10 When forming the name of [Co(NH₃)₅(H₂O)]³⁺, which correctly reflects the naming rules for neutral ligands?
�� Neutral ligand names are ammine and aqua. �� Ligands are arranged alphabetically. �� Ammine precedes aqua.
The ligands present are: 5 NH₃ → pentaammine 1 H₂O → aqua Ligands are named alphabetically before the metal name. Since ammine comes before aqua alphabetically, the correct name is: Pentaammineaquacobalt(III)
- �� Option B → Incorrect alphabetical order.
- �� Option C → "Water" is not the accepted ligand name.
- �� Option D → "Hydrato" is incorrect in this context.
Used
- Definition Matching
Application:
- �� Apply accepted ligand names and alphabetical ordering.
Final Logic:
- �� Ammine comes before aqua alphabetically.
- Ammine Before Aqua
11 In the linkage isomer [Co(NH₃)₅(NO₂)]Cl₂, the complex entity is a cation. How must the central metal be formally named?
�� The coordination entity is positively charged. �� Cationic complexes retain the normal metal name. �� Oxidation state is indicated using Roman numerals.
The coordination entity [Co(NH₃)₅(NO₂)]²⁺ is a cationic complex. According to IUPAC nomenclature, the metal name remains unchanged in cationic and neutral complexes. Therefore, cobalt is named as cobalt(III), where III represents the oxidation state of cobalt. Hence, the correct name of the central metal is cobalt(III).
- �� Option A → The suffix "-ate" is used only for metals present in complex anions.
- �� Option C → "Cobaltic" belongs to older nomenclature and is not accepted in modern IUPAC naming.
- �� Option D → Incorrect oxidation state and obsolete nomenclature.
Used
- Definition Matching
Application:
- �� Determine whether the complex is cationic or anionic.
Final Logic:
- �� Cationic complex → retain the normal metal name.
- Positive Complex = Plain Metal Name
12 In the nomenclature of Hg[Co(SCN)₄], the central metal of the complex anion is named:
�� The coordination entity is an anion. �� Anionic complexes require the suffix "-ate". �� Cobalt becomes cobaltate.
In Hg[Co(SCN)₄], the coordination entity [Co(SCN)₄] is a complex anion. According to IUPAC nomenclature, when the coordination sphere carries a negative charge, the metal name ends with the suffix "-ate". Therefore cobalt is named cobaltate(III).
- �� Option A → Used for cationic or neutral complexes.
- �� Option B → Missing the mandatory "-ate" suffix.
- �� Option D → Mercury is not the central metal of the coordination entity.
Used
- Rule Application
Application:
- �� Apply the naming rule for anionic complexes.
Final Logic:
- �� Anionic complex → metal name ends with "-ate".
- Negative Complex = Add "-ate"
13 The Roman numeral placed in parentheses after the metal's name defines:
�� Roman numerals represent oxidation state. �� Oxidation state is a formal charge. �� It differs from the overall complex charge.
The Roman numeral written after the metal name indicates its oxidation state. Oxidation state is defined as the hypothetical charge that the metal would possess if all ligands and shared electron pairs were completely removed. Thus Option B correctly defines the meaning of the Roman numeral.
- �� Option A → Secondary valence refers to coordination number, not oxidation state.
- �� Option C → Overall charge of the complex may differ from the metal oxidation state.
- �� Option D → Oxidation state has no relation to the number of lone pairs.
Used
- Definition Matching
Application:
- �� Recall the formal definition of oxidation state.
Final Logic:
- �� Roman numeral = oxidation state.
- Roman Numeral = Formal Charge
14 Determine the oxidation state of the central metal in the complex [Pt(NH₃)(H₂O)Cl₂]:
�� NH₃ and H₂O are neutral ligands. �� Each Cl⁻ contributes −1 charge. �� The complex is electrically neutral.
Let the oxidation state of Pt be x. NH₃ = 0 H₂O = 0 2Cl⁻ = −2 Since the complex is neutral: x + 0 + 0 − 2 = 0 x = +2 Therefore, the oxidation state of platinum is +2.
- �� Option A → Would give an overall charge of −2.
- �� Option C → Would give an overall charge of +2.
- �� Option D → Would give an overall charge of −4.
Used
- Substitution
Application:
- �� Form the oxidation-state equation using ligand charges.
Final Logic:
- �� x − 2 = 0, therefore x = +2.
- Neutral Ligands Count as Zero
15 The complex [Ni(H₂O)₆]²⁺ is formed when nickel(II) chloride is dissolved in water. By IUPAC rules, this complex is categorized as a:
�� Only one type of ligand is present. �� The complex has a positive charge. �� Therefore it is homoleptic and cationic.
The complex contains six identical aqua ligands. Since only one type of ligand is present, the complex is homoleptic. The overall charge is +2, making it a cationic complex. Hence [Ni(H₂O)₆]²⁺ is a homoleptic cationic complex.
- �� Option A → The complex is not neutral.
- �� Option B → Only one ligand type is present, so it is not heteroleptic.
- �� Option D → The complex is positively charged, not anionic.
Used
- Definition Matching
Application:
- �� Classify using ligand type and overall charge.
Final Logic:
- �� One ligand type + positive charge = homoleptic cationic.
- One Ligand Type = Homo
16 In the coordination isomer [Co(NH₃)₆][Cr(CN)₆], the [Cr(CN)₆]³⁻ entity represents:
�� [Co(NH₃)₆]³⁺ is the complex cation. �� [Cr(CN)₆]³⁻ is the complex anion. �� Anions are named after cations.
The compound contains: [Co(NH₃)₆]³⁺ → Complex cation [Cr(CN)₆]³⁻ → Complex anion According to IUPAC nomenclature, the cation is named first and the anion is named second. Therefore [Cr(CN)₆]³⁻ represents the complex anion named after the cation.
- �� Option A → Describes the complex cation, not the anion.
- �� Option C → The species carries a −3 charge and is not neutral.
- �� Option D → This is a coordination compound, not a double salt.
Used
- Definition Matching
Application:
- �� Identify the charge and role of each coordination entity.
Final Logic:
- �� Negative coordination entity = complex anion.
- Positive First, Negative Second
17 For the compound [Cr(NH₃)₃(H₂O)₃]Cl₃, how is electrical neutrality achieved in the written formula?
�� The complex ion carries a +3 charge. �� Three chloride ions contribute −3 charge. �� Total charge becomes zero.
The coordination entity [Cr(NH₃)₃(H₂O)₃]³⁺ possesses a +3 charge. Each chloride ion contributes −1 charge. Therefore: (+3) + 3(−1) = 0 The positive charge of the complex cation is exactly balanced by three chloride counter ions, producing an electrically neutral compound.
- �� Option B → NH₃ and H₂O are neutral ligands and cannot neutralize charge.
- �� Option C → No reduction process occurs in formula writing.
- �� Option D → Counter ions are required for charge balance.
Used
- Elimination
Application:
- �� Analyze charge balance in the coordination compound.
Final Logic:
- �� +3 complex charge requires three Cl⁻ ions.
- +3 Needs Three Cl⁻
18 Which formatting rule prevents ambiguity when defining the exact boundaries of the primary and secondary valences in a written chemical formula?
�� Coordination formulas are written continuously. �� Square brackets define the coordination sphere. �� Spaces can create ambiguity.
The square brackets identify the coordination sphere. Writing the metal and ligands continuously within the brackets clearly distinguishes coordinated species from counter ions. Avoiding spaces ensures that the primary and secondary valences are represented unambiguously.
- �� Option A → Roman numerals indicate oxidation state, not formula boundaries.
- �� Option C → Counter ions are written outside the coordination sphere.
- �� Option D → Letter case does not determine coordination boundaries.
Used
- Definition Matching
Application:
- �� Identify the formula-writing rule that defines the coordination sphere.
Final Logic:
- �� No spaces preserve the boundaries of the coordination entity.
- Inside Brackets = No Gaps
19
Based on the passage's explanation, why is 'ammine' placed before 'aqua' in the name triamminetriaquachromium(III) chloride?
�� Ligands are named alphabetically. �� Ligand strength is irrelevant. �� Ammine precedes aqua alphabetically.
According to IUPAC nomenclature, ligand names are arranged alphabetically before the metal name. The names "ammine" and "aqua" are compared alphabetically. Since "ammine" comes before "aqua", it is written first in the compound name.
- �� Option A → Ligand strength does not determine naming order.
- �� Option C → Both ligands are present in equal numbers.
- �� Option D → Oxidation state is independent of ligand order.
Used
- Contextual/Tonal Matching
Application:
- �� Apply the rule explicitly stated in the passage.
Final Logic:
- �� Alphabetical order determines ligand sequence.
- Ammine Before Aqua
20
According to the passage, how is the oxidation number of the chromium metal (+3) deduced from the formula [Cr(NH₃)₃(H₂O)₃]Cl₃?
�� Three chloride ions indicate a +3 complex charge. �� NH₃ and H₂O are neutral ligands. �� Chromium therefore has oxidation state +3.
The three chloride ions outside the coordination sphere contribute a total charge of −3. Therefore, the coordination entity must carry a +3 charge for the compound to remain electrically neutral. Since NH₃ and H₂O are neutral ligands, the entire +3 charge must be contributed by chromium. Hence the oxidation state of chromium is +3.
- �� Option A → Oxidation state is calculated from charge balance, not measured in this manner.
- �� Option B → Neutral ligands contribute zero charge.
- �� Option D → Number of ligands does not determine oxidation state.
Used
- Substitution
Application:
- �� Use charge balance to determine oxidation state.
Final Logic:
- �� Complex charge = +3 and ligand charge = 0, therefore Cr = +3.
- Neutral Ligands → Metal Gives Charge
