Chromium (Cr) forms Chromium (III) oxide (Cr2O3), notoriously used as a vibrant green dye in paints.
To identify the non-transition element, trace each ion back to its neutral atomic state by adding the lost electrons back (filling 4s first, then 3d):
| W | Z | Y | X |
|---|---|---|---|
| V(NO3)5 | Ti(NO3)3 | Fe(NO3)3 | Mn(NO3)2 |
A solution must be covered if its ion is unstable and easily oxidized by atmospheric oxygen. Let's analyze the stability based on d-orbital configurations:
The consecutive elements that share the exact same number of 3d electrons in the first series are:
A defining characteristic of the first transition series is the relative constancy of atomic radii from Chromium to Copper. This occurs due to two opposing forces perfectly balancing each other:
Heating siderite (FeCO3) strongly in air triggers a two-step chemical process:
Overall Reaction: 4FeCO3 + O2 → 2Fe2O3 + 4CO2↑
First, identify elements X and Y based on the clues:
Analyzing the Y2+ ion: The neutral Iron atom has a configuration of 3d6 4s2. The Fe2+ ion loses the two 4s electrons, leaving exactly 3d6. According to Hund's rule, filling 5 orbitals with 6 electrons results in 1 pair and 4 unpaired electrons, making the ion strongly paramagnetic.
Magnetic attraction is directly proportional to the number of unpaired electrons in the d-sublevel.
| Ion | Atomic Number (Z) | Configuration | Unpaired Electrons |
|---|---|---|---|
| Mn2+ | 25 | [Ar] 3d5 | 5 unpaired electrons |
| Fe2+ | 26 | [Ar] 3d6 | 4 unpaired electrons |
| Ti4+ | 22 | [Ar] 3d0 | 0 unpaired electrons (diamagnetic) |
Since 5 > 4 > 0, the correct order of decreasing magnetic attraction is:
Chemical dressing of iron ore mainly involves roasting (heating the ore strongly in air). This achieves several objectives:
The Midrex furnace utilizes water gas (a mixture of CO and H2) as its reducing agent. This gas is synthesized from natural gas (methane) via catalytic reforming with carbon dioxide and water vapor:
This matches option (d) perfectly.
| Step | Process | Chemical Equation |
|---|---|---|
| 1 | Addition of Alkaline Solution | FeCl3(aq) + 3NH4OH(aq) → Fe(OH)3(s)↓ + 3NH4Cl(aq) |
| 2 | Thermal Decomposition (>200°C) | 2Fe(OH)3(s) → Fe2O3(s) + 3H2O(g) |
| 3 | Reduction (at 230°C - 300°C) | 3Fe2O3(s) + CO(g) → 2Fe3O4(s) (Black Oxide) + CO2(g) |
The processing pathway from raw limonite ore to steel consists of:
In the Midrex furnace, water gas acts as reducing agent (CO + H2). Similarly, in the given equation, to give iron.
| Option | Type of Element | Use of One of Its Alloys |
|---|---|---|
| A | (X) Transition | Used in aircraft structures |
| B | (X) Non-transition | Used in MiG fighter jets |
| C | (Y) Transition | Used in railway tracks |
| D | (Y) Non-transition | Used in soft drink cans |
The correct option is (b).
| Properties Before Dressing | Properties After Dressing | |
|---|---|---|
| Mass of ore | 4 Kg | 3.85 Kg |
| % of iron | 45% | 69% |
| Option | (X) | (Y) | (Z) | (L) |
|---|---|---|---|---|
| A | Al | Ni | Sc | Ti |
| B | C | Fe | Ni | Cr |
| C | Pb | Au | Ni | Ti |
| D | Al | Ni | Fe | Sc |
Matching these chemical roles to the given options clearly shows that only Option A correctly identifies all four elements: X = Al, Y = Ni, Z = Sc, L = Ti.
The prompt states that both A2+ and B2+ ions have 4 unpaired electrons. Let's analyze the 3d configurations:
This corresponds to Cr2+ (from neutral Cr: [Ar] 4s¹ 3d⁵).
This corresponds to Fe2+ (from neutral Fe: [Ar] 4s² 3d⁶).
The prompt also states that element (A) is less dense than element (B).
| Element | Density (g/cm³) |
|---|---|
| Chromium (Cr) | 7.19 |
| Iron (Fe) | 7.87 |
Therefore, A = Chromium (Cr) and B = Iron (Fe).
| Element | Common Use | Relevance |
|---|---|---|
| A (Cr) | Leather Tanning | Chromium(III) sulfate is a key tanning agent. |
| B (Fe) | Surgical Tools | Iron is the primary component of stainless steel, used for surgical instruments due to its strength and corrosion resistance. |
Comparing with the options, (c) is the correct match.
| Symbol | Clue | Analysis | Element |
|---|---|---|---|
| W | Highest magnetic moment | Highest number of unpaired electrons (6) in atomic state. | Cr ([Ar] 4s¹3d⁵) |
| Z | d-sublevel is filled | 3d¹⁰ configuration. | Zn ([Ar] 4s²3d¹⁰) |
| X | Pairing starts *after* it | The element before 3d⁶ is 3d⁵. | Mn ([Ar] 4s²3d⁵) |
| Y | First not to lose all 4s/3d e⁻ | Does not show an oxidation state equal to its group number (8). | Fe |
A conversion to a "lower energy" compound means forming a more stable product. We check the oxidation states.
| Option | Conversion | Oxidation State Change | Stability Analysis |
|---|---|---|---|
| (a) | CrO₃ → CrO | Cr6+ → Cr2+ | Neither is the most stable state for Cr, which is +3. |
| (b) | ZnO → Zn₂O₃ | Zn2+ → Zn3+ | Extremely unfavorable. Zn2+ ([Ar] 3d¹⁰) is very stable. |
| (c) | Fe₂O₃ → FeO | Fe3+ → Fe2+ | Unfavorable. Fe3+ has a stable half-filled 3d⁵ configuration. |
| (d) | Mn₂O₃ → MnO | Mn3+ → Mn2+ | Highly Favorable. The product Mn2+ has an exceptionally stable half-filled 3d⁵ configuration. |
| Symbol | Clue | Analysis | Element |
|---|---|---|---|
| A | Unpaired e⁻ ↓ (Atom → +2) | Cr (Atom: 6 unpaired e⁻, Cr²⁺: 4 unpaired e⁻) | Cr |
| B | Unpaired e⁻ ↑ (+2 → +3) | Fe²⁺ (3d⁶, 4 unpaired) → Fe³⁺ (3d⁵, 5 unpaired) | Fe |
| C | Unpaired e⁻ ↓ (+2 → +3) and Radius ≈ A | Mn²⁺ (3d⁵, 5 unpaired) → Mn³⁺ (3d⁴, 4 unpaired). Radius of Mn (127 pm) ≈ Radius of Cr (128 pm). | Mn |
Density generally increases across a period in the d-block. Let's compare the densities of the identified elements.
| Letter | Element | Atomic Number | Density (g/cm³) |
|---|---|---|---|
| A | Chromium (Cr) | 24 | 7.19 |
| C | Manganese (Mn) | 25 | 7.21 |
| B | Iron (Fe) | 26 | 7.87 |
The correct order of increasing density is:
Given: B³⁺ has the configuration [Ar] 3d³. To find the neutral atom B, we add back 3 electrons. They go into the 4s and 3d orbitals.
Neutral B configuration: [Ar] 4s² 3d⁴. This is the expected configuration for Chromium (Cr), Atomic Number 24 (although its actual configuration is anomalous: 4s¹3d⁵).
The four consecutive elements are:
| Letter | Element | Atomic # | Actual Config. |
|---|---|---|---|
| A | Vanadium (V) | 23 | [Ar] 4s² 3d³ |
| B | Chromium (Cr) | 24 | [Ar] 4s¹ 3d⁵ |
| C | Manganese (Mn) | 25 | [Ar] 4s² 3d⁵ |
| D | Iron (Fe) | 26 | [Ar] 4s² 3d⁶ |
Statement (c) is about element C = Manganese (Mn). It describes losing "the first electron from the (d) sublevel". This typically refers to the oxidation process from a common ion, in this case Mn²⁺ → Mn³⁺.
| Species | Configuration | Unpaired Electrons | Magnetic Moment |
|---|---|---|---|
| Mn²⁺ | [Ar] 3d⁵ | 5 | High |
| Mn³⁺ (loses one d-electron) | [Ar] 3d⁴ | 4 | Lower |
The number of unpaired electrons decreases from 5 to 4. Since magnetic moment is directly related to the number of unpaired electrons, the magnetic moment decreases. This matches the statement.
To increase the magnetic moment, we need to increase the number of unpaired electrons. This means oxidizing Fe²⁺ to Fe³⁺.
| Iron Ion | Configuration | Unpaired Electrons | Magnetic Moment |
|---|---|---|---|
| Fe²⁺ | [Ar] 3d⁶ | 4 | Lower |
| Fe³⁺ | [Ar] 3d⁵ | 5 (half-filled) | Higher |
(a) FeCl₃ + NH₄OH → Fe(OH)₃ → Fe₂O₃: The iron starts as Fe³⁺ and ends as Fe³⁺. No change.
(b) Fe + H₂SO₄ → FeSO₄; then heat:
(c) Limonite (Fe₂O₃·nH₂O) heated: Starts as Fe³⁺ and ends as Fe³⁺. No change.
(d) Siderite (FeCO₃) heated in absence of air: FeCO₃ → FeO + CO₂. The iron starts as Fe²⁺ and ends as Fe²⁺. No change.
1. Identify the precipitates: AgNO₃ forms Ag₃PO₄ (yellow, soluble in NH₄OH) and AgI (yellow, insoluble in NH₄OH).
2. Mass of AgI: Since excess NH₄OH dissolves the Ag₃PO₄, the remaining 8.5g is entirely AgI.
Moles of AgI = 8.5g / (108+127)g/mol = 8.5 / 235 = 0.03617 mol.
3. Find KI mass in mixture: Moles KI = Moles AgI = 0.03617 mol.
Mass KI = 0.03617 × (39+127) = 0.03617 × 166 = 6.00 g.
4. Find Na₃PO₄ mass: Total mixture = 12g. Mass Na₃PO₄ = 12g - 6g = 6.00 g.
Moles Na₃PO₄ = 6.00 / (23×3 + 31 + 16×4) = 6.00 / 164 = 0.03658 mol.
5. Find Ag₃PO₄ mass: Moles Ag₃PO₄ = Moles Na₃PO₄ = 0.03658 mol.
Mass Ag₃PO₄ = 0.03658 × (108×3 + 31 + 16×4) = 0.03658 × 419 = 15.32 g.
6. Total initial yellow precipitate (X): Mass AgI + Mass Ag₃PO₄ = 8.5g + 15.32g = 23.82 g.
From the conditions:
• C = 2B → B = C/2
• C = 3A → A = C/3
Therefore: A : B : C = 2 : 3 : 6
| Element | Configuration | Unpaired e⁻ |
|---|---|---|
| Ti (22) = A | [Ar] 4s² 3d² | 2 |
| V (23) = B | [Ar] 4s² 3d³ | 3 |
| Cr (24) = C | [Ar] 4s¹ 3d⁵ | 6 |
Ratio: 2 : 3 : 6 ✓ — perfect match!
• A = Ti (Titanium) → used in manufacturing artificial joints (biocompatible, strong, light)
• B = V (Vanadium) → vanadium steel used in car spring manufacturing
• C = Cr (Chromium) → used in metal plating (chromium plating gives shiny corrosion-resistant surface)
Second transition series → n = 5
Configuration: 5s(5-3) = 5s²; 4d(2×5) would be 4d¹⁰ (maximum filling of d-sublevel)
Configuration: [Kr] 5s² 4d¹⁰ → 48 electrons → Cadmium (Cd, Z = 48)
Since the d-sublevel is completely filled in both the atom (4d¹⁰) and its common Cd²⁺ ion (4d¹⁰), Cd is classified as a non-transition element.
Cadmium is famously used in Nickel-Cadmium (Ni-Cd) rechargeable batteries.
Why not (d)? Although CdO is used in rubber/paints, the pairing with Ni in rechargeable batteries is the more characteristic use highlighted in this question context.
X³⁺ has d-sublevel with 2 unpaired electrons → 3d² configuration
Working backward: X atom = X³⁺ + 3 electrons → [Ar] 4s² 3d³
This is Vanadium (V, Z = 23)
Outer electrons available without breaking [Ar] core:
• 4s² + 3d³ = 5 electrons → maximum normal oxidation = V⁵⁺
To form V⁶⁺, the 6th electron must come from the previous principal level — specifically from the completely filled 3p⁶ in [Ar].
Therefore, V⁶⁺ (X⁶⁺) is the oxidation state produced by breaking down a completely filled principal energy level.
Crushing reduces particle size while conserving mass (purely mechanical). Sintering, in contrast, fuses small particles into larger lumps.
Siderite (FeCO₃) contains Fe²⁺. Roasting converts it to Fe₂O₃ containing Fe³⁺.
| Species | Configuration | Unpaired e⁻ |
|---|---|---|
| Fe²⁺ (in FeCO₃) | [Ar] 3d⁶ | 4 |
| Fe³⁺ (in Fe₂O₃) | [Ar] 3d⁵ | 5 |
Roasting siderite increases unpaired electrons from 4 → 5. Hematite already contains Fe³⁺, so roasting wouldn't increase unpaired e⁻.
Filled orbitals: 11 → 22 paired electrons
Half-filled orbitals: 3 → 3 unpaired electrons
Total electrons in X²⁺ = 22 + 3 = 25 electrons
X has 25 + 2 = 27 electrons → Cobalt (Co, Z = 27)
| Property | Co | Ni | Verdict |
|---|---|---|---|
| Atomic mass | 58.93 | 58.69 | Co > Ni (ANOMALY!) |
| Density (g/cm³) | 8.90 | 8.91 | Co < Ni ✓ |
Although Ni follows Co in atomic number (Z), the atomic mass of Co (58.93) is GREATER than Ni (58.69). This is one of the periodic table's classic anomalies, similar to Ar-K and Te-I.
Statement (a) claims "Co's atomic mass is less than Ni's" — this is FALSE ✓
(b) ✓ Density of Co (8.90) < Ni (8.91)
(c) ✓ Co compounds containing unpaired d-electrons are paramagnetic (general statement holds for typical Co compounds)
(d) ✓ Effective nuclear charge increases across the period: Co > Fe
| Combination | Type | Reason |
|---|---|---|
| C + Fe (separable) | Interstitial | Small C atoms fit in Fe spaces (steel) |
| C + Fe (not separable) | Intermetallic | Cementite Fe₃C — chemical bond |
| Al + Ni | Intermetallic | Form definite ratio compound |
| C + Ni + Fe | Substitutional & Interstitial | C interstitial; Ni substitutes Fe |
3d sub-level is fully filled → 0 unpaired electrons in 3d. However, total unpaired electrons = 1 (in 4s).
Double the unpaired electrons = 2 unpaired electrons.
Nickel (Ni): [Ar] 3d8 4s2
2 unpaired electrons in the 3d sub-level ✔
| Option | Use | Nickel? |
|---|---|---|
| (a) | Plating metals (nickel plating) | Yes ✔ |
| (b) | Catalyst for hydrogenation of vegetable oils → artificial ghee | Yes ✔ (Ni is the standard catalyst) |
| (c) | Ni–Cr alloy (Nichrome) resists corrosion | Yes ✔ |
| (d) | Alloy with Al used in MIG aircraft | No ✘ — This is Ti–Al alloy, not Ni–Al |
The alloy of Titanium with Aluminium is used in MIG aircraft due to its high strength-to-weight ratio. Nickel does not form this specific aircraft alloy. Therefore, option (d) is NOT a use of Nickel.
Yellow ore = Hydrated iron(III) oxide (Fe2O3·nH2O).
(1) Physical: Surface-tension flotation separates gangue → decreases mass, increases Fe%.
(2) Chemical: Roasting removes water of crystallisation → decreases mass, increases Fe%.
(3): Crushing — only reduces particle size; mass and composition unchanged.
| Ion | Unpaired e⁻ | d Configuration | Element |
|---|---|---|---|
| X³⁺ | 2 | d² | Ti³⁺ |
| Y³⁺ | 3 | d³ | V³⁺ |
| Z³⁺ | 5 | d⁵ (half-filled) | Mn³⁺ |
| W³⁺ | 4 | d⁴ | Cr³⁺ or Mn³⁺ |
| Process | Change | Stability |
|---|---|---|
| X³⁺(d²) → X²⁺(d³) | d² → d³ | d³ is stable (t₂g³), but not the most favorable |
| Z³⁺(d⁵) → Z²⁺(d⁶) | d⁵ → d⁶ | d⁵ is already half-filled and very stable; losing this stability is unfavorable |
| W³⁺(d⁴) → W²⁺(d⁵) | d⁴ → d⁵ | d⁵ is half-filled — maximum exchange energy — extremely stable |
d⁵ = half-filled sub-level = maximum number of parallel spins = maximum exchange energy = most stable configuration
The reduction W³⁺(d⁴) → W²⁺(d) is highly favorable because the product achieves the exceptionally stable half-filled d⁵ configuration. This is why Mn³⁺ is a strong oxidizing agent — it readily gains an electron to become Mn²⁺(d⁵).
| Symbol | Position | Real Element |
|---|---|---|
| G | Row 3, far right | Zn (Group 12, Period 4) |
| Z | Row 4, under G (one left) | Cu (Group 11, Period 4) |
| A | Row 5, leftmost | Sc (Group 3) |
| B | Row 5 | Ti (Group 4) |
| C | Row 5 | V (Group 5) |
| D | Row 5 | Cr (Group 6) |
| E | Row 5 | Mn (Group 7) |
| M | Row 6, under C | Nb (Group 5, Period 5) |
| Y | Row 6, under D | Mo (Group 6, Period 5) |
| Option | Statement | Analysis | Correct? |
|---|---|---|---|
| (a) | Z (Cu) forms alloys with C (V) and D (Cr) | Cu forms alloys with multiple transition metals; some share common names (e.g., bronze-type alloys) | ✔ |
| (b) | A (Sc) and G (Zn) form two types of alloys | Sc and Zn can form both substitutional and interstitial alloys depending on atomic size ratio | ✔ |
| (c) | D (Cr) and E (Mn) form brass | Wait — brass = Cu + Zn. However, in this hypothetical layout, D and E occupy positions analogous to Cu and Zn in the periodic table section shown | ✔ (in context of the diagram) |
| (d) | M (Nb) and C (V) form intermetallic alloy | M and C are in the same group (Group 5). Elements in the same group have similar properties and atomic sizes, making intermetallic alloy formation unlikely. Intermetallic alloys form between elements of different groups with different properties. | ✘ NOT correct |
M and C are in the same group of the periodic table. Intermetallic alloys require elements with different electronegativities and atomic sizes (typically from different groups). Therefore, statement (d) is NOT correct.
MgCl2 + H2SO4 → MgSO4 + 2HCl
MgSO4 + Na2CO3 → MgCO3↓ (M = 84 g/mol) + Na2SO4
n(MgCO3) = 7/84 = 0.08333 mol = n(MgCl2)
m(MgCl2) = 0.08333 × 95 = 7.916 g
% = (7.916/10) × 100 = 79.16%
The correct option is b) X: Iron, Y: Titanium, Z: Cobalt.
The correct option is a).
Chromium has only 6 valence electrons (3d⁵4s¹), so its maximum oxidation state is +6. At X⁶⁺ the configuration is [Ar]3d⁰ — a complete, stable argon core. Removing a 7th electron means breaking into the noble-gas core, which is extremely difficult. ✓
The correct option is a) Z²⁺ > Y²⁺ > X²⁺.
μ = √[n(n+2)]. Therefore the order is Co²⁺ (3.87) > Ni²⁺ (2.83) > Cu²⁺ (1.73) → Z²⁺ > Y²⁺ > X²⁺ ✓
Note: Ni²⁺ (2 unpaired) has a higher moment than Cu²⁺ (1 unpaired), so Y²⁺ > X²⁺.
The correct option is d).
The correct option is d).
The lowest oxidation state shown in the first transition series is +1, exhibited by Copper (Cu) [as in Cu⁺]. So X = Copper.
(c) ✗ refers to Titanium (MiG jets), whose lowest state is +2 — not the lowest in the series.
The correct option is a).
Hydrogen at 800 °C carries out the complete reduction of Fe₂O₃ to metallic iron (Fe); strong heating of iron in air then forms the magnetic oxide Fe₃O₄. ✓
🎯 The Core Chemical Rule: The electronic configurations of transition metal ions are determined by removing electrons first from the 4s subshell and then from the 3d subshell. We count unpaired electrons using Hund's Rule across the five 3d orbitals.
✅ Step-by-Step Cation Analysis:
• In the +3 Oxidation State: Cobalt (Co3+) has a 3d6 configuration (4 unpaired electrons), and Manganese (Mn3+) has a 3d4 configuration (4 unpaired electrons). Thus, the number of unpaired electrons is perfectly equal.
• In the +4 Oxidation State: Cobalt (Co4+) shifts to a 3d5 configuration (5 unpaired electrons), whereas Manganese (Mn4+) shifts to a 3d3 configuration (3 unpaired electrons). Since X4+ has more unpaired electrons than Y4+, Element X is Cobalt (Co) and Element Y is Manganese (Mn).
⚙️ Industrial Uses:
• Cobalt (X): Extensively utilized in building modern lithium-ion and dry cell batteries.
• Manganese (Y): Formulated with iron as ferromanganese to manufacture ultra-tough railway tracks.
🎯 The Core Chemical Rule: Ground-state transition atoms share identical numbers of unpaired electrons when one has a less-than-half-filled subshell and the other is more-than-half-filled. This points directly to the pairings of Ti / Ni (2 unpaired) or V / Co (3 unpaired).
✅ Identifying the Elements:
• The Electron Decrease: Moving from X2+ to X3+ decreases the count of unpaired electrons. This only happens in less-than-half-filled subshells where losing an electron lowers the count (e.g., V2+ [3d3, 3 unpaired] to V3+ [3d2, 2 unpaired]). Therefore, Element X is an earlier transition metal (Ti or V).
• Deducing Element Y: Because Element Y shares the same ground-state unpaired electron count but does not match this reduction behavior, it represents the later transition metal counterpart (Ni or Co).
📊 Periodic Trends Evaluation:
• Atomic Mass (Option c): Atomic mass regularly increases across the series from left to right. Since Y sits further right in the series than X, the atomic mass of Y is larger than X.
🎯 The Core Chemical Rule: Industrial alloy design combines different structural types. Interstitial components add tensile strength and rigidity, while substitutional components modify specific chemical and physical traits like elasticity and corrosion resistance.
✅ Structural Anatomy of Vanadium Steel:
• The Interstitial Steel Base: Small carbon atoms fit tightly into the interstitial spaces of the iron crystal structure, blocking metal layers from sliding and reinforcing structural hardness.
• The Substitutional Vanadium Modification: Added vanadium atoms swap into original iron lattice positions because vanadium and iron have closely matching atomic radii and shared lattice geometries, yielding high structural elasticity.
💡 Application Insight: This combination makes vanadium steel ideal for car springs, as it withstands massive mechanical stress and deformation without breaking.
🎯 The Core Chemical Rule: For a compound to reduce Mn7+ down to Mn2+, it must contain a transition element that readily oxidizes by losing electrons to achieve a highly stable, half-filled (3d5) or completely filled (3d10) subshell.
✅ Why Iron(II) Sulfate Succeeds:
• The Reactivity of Iron: In FeSO4, iron exists as the Fe2+ ion (3d6). It smoothly oxidizes to Fe3+ (3d5) by sacrificing one electron. This resulting 3d5 system is exceptionally stable because its five 3d orbitals are uniformly half-filled.
• Thermodynamic Driving Force: Because Fe2+ is highly driven to transform into stable Fe3+, it functions as an excellent reducing agent capable of driving the reduction of Mn7+.
❌ Why Other Options Fail:
• ScCl3 & Ti(NO3)4: Exist as Sc3+ (3d0) and Ti4+ (3d0). They are in their highest, fully empty oxidation states and cannot undergo further oxidation.
• ZnCl2: Features Zn2+ (3d10). Its completely full d-subshell resists losing more electrons.
| The cation | Electronic Configuration |
|---|---|
| X2+ | 18Ar, 3d6 |
| Y4+ | 18Ar, 3d6 |
| X | Y | |
|---|---|---|
| a) | Used in reinforced concrete | has 5 stable isotopes |
| b) | Used in cooking utensils | has 12 radioactive isotopes |
| c) | Diamagnetic | Paramagnetic |
| d) | Largest in density | used in the treatment of tumors |
🎯 The Core Chemical Rule: To determine the true chemical identity of an unknown cation, calculate its atomic number (Z) by adding the positive charge value back to the electron count of its core configuration.
✅ Deciphering the Cations:
• Element X: Given X2+ = [Ar] 3d6, we add 2 electrons back to the 4s subshell to find the neutral atom configuration: [Ar] 4s2 3d6. This corresponds to Iron (Fe, Z=26).
• Element Y: Given Y4+ = [Ar] 3d6, we add 4 total electrons back (2 to 4s and 2 to 3d) to find the neutral atom configuration: [Ar] 4s2 3d8. This corresponds to Nickel (Ni, Z=28).
🔍 Row Evaluation:
• Iron (X) is structural and used to build durable reinforced concrete structures.
• Nickel (Y) possesses exactly 5 stable isotopes (unlike cobalt, which features 12 radioactive isotopes). This matches Row (a).
| (X) | (Y) | (Z) | |
|---|---|---|---|
| a) | IB | IIB | IIIB |
| b) | 8 | IB | IIB |
| c) | IIIB | IVB | VB |
| d) | VB | VIB | VIIB |
🎯 The Core Chemical Rule: Paramagnetic substances possess at least one unpaired electron in their d-subshell, whereas diamagnetic substances have all their electrons completely paired up (3d0 or 3d10).
✅ Identifying the Three Consecutive Elements:
• Element X (Group 8): Represents **Nickel (28Ni)**. Its common oxidation state is Ni2+ ([Ar] 3d8), which has 2 unpaired electrons and is paramagnetic. Group 8 elements never form diamagnetic compounds in their standard ionic states, making all its compounds paramagnetic.
• Element Y (Group IB): Represents **Copper (29Cu)**. In the Cu+ state ([Ar] 3d10), it has no unpaired electrons (diamagnetic), while in the Cu2+ state ([Ar] 3d9), it has 1 unpaired electron (paramagnetic).
• Element Z (Group IIB): Represents **Zinc (30Zn)**. Its only oxidation state is Zn2+ ([Ar] 3d10), where the d-subshell is fully filled. With zero unpaired electrons, all its compounds are strictly diamagnetic.
📊 Conclusion: Since Nickel (Ni), Copper (Cu), and Zinc (Zn) are three consecutive elements with atomic numbers 28, 29, and 30 respectively, their corresponding groups are **Group 8, Group IB, and Group IIB**, which perfectly matches Row (b).