d and f Block Elements Class 12 PDF: Complete NEET Revision Notes

01
Introduction to d- and f-Block Elements

In the expansive world of Inorganic Chemistry, mastering the transition and inner transition metals is a top priority for medical aspirants. This d and f block elements class 12 pdf guide provides a high-yield breakdown of elements that occupy the central and bottom portions of the periodic table. These elements are characterized by the gradual filling of (n−1)d and (n−2)f orbitals, leading to unique chemical behaviors like variable oxidation states, colorful compounds, and magnetic properties.

GENERAL ELECTRONIC CONFIGURATION
d-Block: (n−1)d1−10 ns1−2
f-Block: (n−2)f1−14 (n−1)d0−1 ns2

02
Position in the Periodic Table

The d-block occupies the central part of the periodic table, bridging the gap between the reactive s-block metals and the covalent p-block elements. The f-block, consisting of two series of 14 elements each, is placed at the bottom to maintain the structure of the periodic table.

D-BLOCK PLACEMENT Found in groups 3 to 12 across periods 4, 5, 6, and 7.
F-BLOCK PLACEMENT Belong to Group 3; Lanthanides are in Period 6 and Actinides are in Period 7.

03
Electronic Configuration & Stability Trends

The filling of d and f orbitals follows the Aufbau principle, but stability often dictates exceptions. For instance, half-filled and fully-filled configurations provide extra stability due to symmetry and exchange energy.

WARN
Always remember the exceptions for Chromium (Cr: 3d5 4s1) and Copper (Cu: 3d10 4s1). This stability is critical for your d and f block elements class 12 pdf revision.
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04
General Physical & Chemical Properties

Transition metals exhibit high metallic character. They are hard, have high melting and boiling points, and possess high densities. Their chemical versatility stems from their ability to use both ns and (n−1)d electrons for bonding.

Property Trend / Description Reasoning
Metallic Character Very high; hard and ductile. Strong metallic bonding involving d-electrons.
Atomic Radii Decreases then remains constant. Increased nuclear charge vs screening effect.
Ionization Enthalpy Increases across the period. Increase in effective nuclear charge.

05
Variable Oxidation States

One of the most defining characteristics of transition elements is their ability to exhibit multiple oxidation states. This occurs because the energy difference between the ns and (n−1)d orbitals is very small.

Manganese (Mn) shows the maximum number of oxidation states in the 3d series, ranging from +2 to +7.

06
Colored Compounds and d-d Transitions

Most transition metal ions form colored compounds. The color is due to the absorption of visible light, which excites electrons between different energy d-orbitals. This concept is fundamental in your d and f block elements class 12 pdf guide.

TIP
Compounds of Sc3+ (3d0) and Zn2+ (3d10) are colorless because they either have no d-electrons or no vacant space for d-d transitions.

07
Magnetic Properties

Transition elements often exhibit paramagnetism due to the presence of unpaired electrons. The magnetic moment can be calculated using the spin-only formula.

SPIN-ONLY FORMULA
μ = √[n(n+2)] BM
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08
Catalytic Properties and Alloy Formation

Transition metals are efficient catalysts because of their variable oxidation states and their ability to form complex intermediates. Examples include Fe in the Haber Process and V2O5 in the Contact Process.

09
Important Compounds: K2Cr2O7 and KMnO4

Potassium Dichromate and Potassium Permanganate are heavy-weight topics. They act as strong oxidizing agents and are indispensable in volumetric analysis as taught in the d and f block elements class 12 pdf.

In acidic medium: MnO4 + 8H+ + 5e → Mn2+ + 4H2O

10
f-Block Elements: The Lanthanides

The 14 elements from Cerium (58) to Lutetium (71) are called Lanthanides. The most significant trend in this series is the Lanthanide Contraction, which affects the sizes of transition metals in the 5d series.

LANTHANIDE CONTRACTION
Cause: Poor shielding effect of 4f electrons. Consequence: Similar atomic radii of 4d and 5d elements (e.g., Zr and Hf).

11
Actinides: The Radioactive Series

Unlike Lanthanides, all Actinides are radioactive. They exhibit a wider range of oxidation states (up to +7) because the 5f, 6d, and 7s levels are comparable in energy levels.

Quick Revision Summary

  • Transition elements have incomplete d-subshells in ground or ionic states.
  • Zn, Cd, and Hg are d-block elements but NOT transition elements.
  • Magnetic moment μ = √[n(n+2)] BM.
  • Color results from d-d transitions in ions with unpaired electrons.
  • KMnO4 acts as an oxidant in acidic, neutral, and alkaline media.
  • Lanthanide contraction leads to the similarity of Zr and Hf sizes.
  • Actinides show higher oxidation states than Lanthanides.
  • K2Cr2O7 is used in the chromyl chloride test.
  • Alloys are formed due to similar atomic radii of transition metals.
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12
Frequently Asked Questions

Why is BF3 non-polar despite polar B-F bonds?
BF3 has a symmetrical trigonal planar geometry. The vector sum of the three B-F bond dipoles is zero, making the net dipole moment μ = 0.
How does a lone pair affect the bond angle?
Lone pairs occupy more space and exert greater repulsion on bond pairs. This causes the bond pairs to push closer together, reducing the bond angle.
What is the bond order of O2 and O2+?
The bond order of O2 is 2. When it loses an electron to form O2+, the electron is removed from an anti-bonding orbital, increasing the bond order to 2.5.
What are the conditions for Hydrogen bonding?
1. Hydrogen must be bonded to a highly electronegative atom (F, O, or N). 2. The electronegative atom must be small in size to provide concentrated charge density.
Is every molecule with an expanded octet unstable?
No. Molecules like SF6 and PCl5 are stable because the central atom can use its d-orbitals to accommodate more than 8 electrons.
What is the main difference between Sigma and Pi bonds?
Sigma bonds are formed by end-to-end overlap and allow free rotation, while Pi bonds are formed by lateral overlap and prevent rotation around the bond axis.

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Table of Contents — Chemistry Class 12

Table of Contents

Chemistry — Class 12

01SolutionsGo to page
02ElectrochemistryGo to page
03Chemical KineticsGo to page
04d- and f-Block ElementsGo to page
05Coordination CompoundsGo to page
06Haloalkanes and HaloarenesGo to page
07Alcohols, Phenols and EthersGo to page
08Aldehydes, Ketones and Carboxylic AcidsGo to page
09AminesGo to page
10BiomoleculesGo to page

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