d and f block elements shots notes cum cheat sheets, Cheat Sheet of Chemistry

The d and f-block elements occupy the central part of the periodic table (Groups 3 to 12). An element is classified as a transition metal if it has a partially filled d-subshell in its ground state or in any of its common oxidation states.

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🧪 D- AND F-BLOCK ELEMENTS HIGH-YIELD
BLUEPRINT
Lanthanoid Contraction, Chromate Profiles & Permanganate Redox Equations
This study blueprint condenses the absolute highest-priority inorganic trends, conversions, and chemical logic
from the D- and F-block chapter into direct, rule-based checklists for efficient recall.
1. Lanthanoid Contraction & Its Direct Consequences
As the atomic number increases within the 4f-series (Lanthanoids), the atomic and ionic radii exhibit a steady,
continuous decrease. This shrinkage is driven by the exceptionally poor shielding effect of 4f electrons,
enabling the rising nuclear charge to pull the outer shell inward.
The Size Equalizer Pairs: Due to this contraction, elements belonging to the 2nd (4d) and 3rd (5d) transition
series exhibit practically identical atomic radii. NTA targets these specific matching twins:
• Zr ≈ Hf (Zirconium ≈ Hafnium) — Sizes: Zr 160 pm, Hf 159 pm
• Nb ≈ Ta (Niobium ≈ Tantalum)
Basicity Trend of Hydroxides: Following Fajan's rules, covalent character grows as size decreases from
La3+ to Lu3+. Thus, the capability to release OH- drops systematically:
La(OH)3 [Most Basic] > ... > Lu(OH)3 [Least Basic]
Ionization Enthalpy Shift: The 5d elements require significantly higher ionization energy than 3d and 4d
elements because their compressed atomic clouds hold onto valence shell electrons with maximum affinity.
2. Chromate-Dichromate Interconversion (pH Dependent)
The chemical equilibrium between the tetrahedral Chromate ion (CrO4
2-) and the corner-sharing twin tetrahedral
Dichromate ion (Cr2O7
2-) in solution relies strictly on the pH of the surrounding medium:
🔄 THE PH BALANCE EQUATIONS
In Acidic Medium (pH < 7): Yellow chromate absorbs H+ and quickly dimerizes into orange dichromate.
2CrO4
2- (Yellow) + 2H+ Cr2O7
2- (Orange) + H2O
In Basic Medium (pH > 7): Hydroxyl ions drive orange dichromate back down into the monomeric yellow
form.
Cr2O7
2- (Orange) + 2OH- 2CrO4
2- (Yellow) + H2O
NEET Inorganic Chemistry Core Series &bull; High-Yield Master Sheet Page 1
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🧪 D- AND F-BLOCK ELEMENTS HIGH-YIELD

BLUEPRINT

Lanthanoid Contraction, Chromate Profiles & Permanganate Redox Equations

This study blueprint condenses the absolute highest-priority inorganic trends, conversions, and chemical logic from the D- and F-block chapter into direct, rule-based checklists for efficient recall.

1. Lanthanoid Contraction & Its Direct Consequences

As the atomic number increases within the 4f-series (Lanthanoids), the atomic and ionic radii exhibit a steady, continuous decrease. This shrinkage is driven by the exceptionally poor shielding effect of 4f electrons, enabling the rising nuclear charge to pull the outer shell inward.

The Size Equalizer Pairs: Due to this contraction, elements belonging to the 2nd (4d) and 3rd (5d) transition series exhibit practically identical atomic radii. NTA targets these specific matching twins:

  • Zr ≈ Hf (Zirconium ≈ Hafnium) — Sizes: Zr ∼ 160 pm, Hf ∼ 159 pm
  • Nb ≈ Ta (Niobium ≈ Tantalum) Basicity Trend of Hydroxides: Following Fajan's rules, covalent character grows as size decreases from La3+^ to Lu3+. Thus, the capability to release OH-^ drops systematically: La(OH) 3 [Most Basic] > ... > Lu(OH) 3 [Least Basic] Ionization Enthalpy Shift: The 5d elements require significantly higher ionization energy than 3d and 4d elements because their compressed atomic clouds hold onto valence shell electrons with maximum affinity.

2. Chromate-Dichromate Interconversion (pH Dependent)

The chemical equilibrium between the tetrahedral Chromate ion (CrO 4 2-) and the corner-sharing twin tetrahedral Dichromate ion (Cr 2 O 7 2-) in solution relies strictly on the pH of the surrounding medium:

🔄 THE PH BALANCE EQUATIONS

  • In Acidic Medium (pH < 7): Yellow chromate absorbs H+^ and quickly dimerizes into orange dichromate. 2CrO 4 2-^ (Yellow) + 2H+^ Cr 2 O 7 2-^ (Orange) + H 2 O
  • In Basic Medium (pH > 7): Hydroxyl ions drive orange dichromate back down into the monomeric yellow form. Cr 2 O 7 2-^ (Orange) + 2OH-^ 2CrO 4 2-^ (Yellow) + H 2 O

NEET Inorganic Chemistry Core Series • High-Yield Master Sheet Page 1

⚠️ THE FIXED OXIDATION STATE TRAP

NTA frequently tries to deceive students into classifying this interconversion as a redox pathway. It is NOT a redox reaction! The oxidation state of Chromium remains a rigid, unchanging +6 in both yellow chromate and orange dichromate ions.

3. Potassium Permanganate (KMnO 4 ) Redox Engine

Potassium Permanganate acts as a phenomenal oxidizing agent. However, its stoichiometry and net electron exchange vary across media environments.

🔑 THE "BAN-153" VALENCY CODE

To avoid deriving complex half-cell conversions, memorize this speed shortcut for the valency factor (n- factor):

  • Basic / Neutral Medium → Converts to MnO 2 (+7 → +4 change) ⇒ N = 3
  • Acidic Medium → Converts to Mn2+^ (+7 → +2 change) ⇒ N = 5
  • Strongly Nalkaline Medium → Converts to MnO 4 2-^ (+7 → +6 change) ⇒ N = 1

Acidic Oxidation Checklist (n = 5): Under sulfuric acid environments, KMnO 4 targets and transforms chemical species as follows:

Iodide (I-) → Oxidized into molecular I 2 gas Ferrous (Fe2+) → Oxidized into stable ferric Fe3+ Oxalate (C 2 O 4 2-) → Cleaved and liberated as gaseous CO 2 Sulphide (S2-) → Precipitated out as free elemental S

NEET Inorganic Chemistry Core Series • High-Yield Master Sheet Page 2