Search This Blog

Exam Master Review Sheet - p-Block Elements

Chemca Formula Sheet - p-Block Elements

CHEMCA

EXAM MASTER FORMULA SHEET

The p-Block Elements (Groups 13-18)

Strategic Revision for JEE Main, Advanced & NEET

1. General Characteristics & Key Effects

The Inert Pair Effect

The reluctance of $ns^2$ valence electrons to participate in bonding due to poor shielding by intervening $d$ and $f$ orbitals. As we go down the group, the lower oxidation state becomes more stable.

Gr 13 (+3, +1): $\ce{Tl+ > Tl^3+}$
Gr 14 (+4, +2): $\ce{Pb^2+ > Pb^4+}$
Gr 15 (+5, +3): $\ce{Bi^3+ > Bi^5+}$
Anomalous Behavior of 1st Elements

The first element of each group (B, C, N, O, F) behaves differently from the rest of its group members due to:

  • Smallest size & high electronegativity.
  • High ionization enthalpy.
  • Absence of vacant d-orbitals: Restricts their maximum covalency to 4 (e.g., $\ce{BF4-}$ exists, but $\ce{BF6^3-}$ does not).

2. Group 13 (Boron) & Group 14 (Carbon)

Diborane ($\ce{B2H6}$) Group 13

An electron-deficient dimer. Boron is $sp^3$ hybridized.

$4 \times (\ce{B-H})$ terminal bonds ($2c-2e$)
$2 \times (\ce{B-H-B})$ bridge bonds ($3c-2e$)

Banana bonds restrict rotation. Terminal atoms are coplanar.

Key Boron Compounds:
  • Orthoboric Acid ($\ce{H3BO3}$): A weak monobasic Lewis acid. It does not donate a proton; it accepts an $\ce{OH-}$ from water: $\ce{B(OH)3 + 2H2O <=> [B(OH)4]- + H3O+}$.
  • Borazine ($\ce{B3N3H6}$): Inorganic benzene. Isoelectronic and isostructural with benzene, but more reactive due to bond polarity.
Carbon Allotropes Group 14
  • Diamond: $sp^3$ hybridized, rigid 3D network, hardest natural substance, electrical insulator.
  • Graphite: $sp^2$ hybridized, layered structure held by van der Waals forces. Good conductor (free $\pi$ electrons), acts as a lubricant.
  • Fullerenes: E.g., $\ce{C60}$. Contains 20 six-membered rings and 12 five-membered rings. Purest form of carbon.
Silicones & Silicates:
  • Silicates: Basic structural unit is $\ce{SiO4^4-}$ (tetrahedral).
  • Silicones: Synthetic organosilicon polymers containing $\ce{R2SiO}$ repeating units. Highly water-repellent (hydrophobic) and thermally stable.

3. Group 15 (Pnictogens)

Group 15
Action of $\ce{HNO3}$ on Metals (V. IMP)
Copper (Cu) $\ce{Dilute -> NO (g)}$
$\ce{Conc. -> NO2 (g)}$
Zinc (Zn) $\ce{Dilute -> N2O (g)}$
$\ce{Conc. -> NO2 (g)}$
Industrial Processes
  • Haber's Process ($\ce{NH3}$):
    $\ce{N2 + 3H2 <=>[Fe / Mo][700K, 200 atm] 2NH3}$
  • Ostwald's Process ($\ce{HNO3}$):
    Catalytic oxidation of $\ce{NH3}$ over $Pt/Rh$ gauge at 500K to yield $\ce{NO}$, which is oxidized to $\ce{NO2}$ and dissolved in water.
Oxoacids of Phosphorus (Structure Dictates Function)
Formula & Name Ox. State Bonds Basicity Reducing Nature
$\ce{H3PO2}$ (Hypophosphorous) +1 $1 (\ce{P=O}), 1 (\ce{P-OH}), \mathbf{2 (\ce{P-H})}$ Monobasic Strong
$\ce{H3PO3}$ (Orthophosphorous) +3 $1 (\ce{P=O}), 2 (\ce{P-OH}), \mathbf{1 (\ce{P-H})}$ Dibasic Moderate
$\ce{H3PO4}$ (Orthophosphoric) +5 $1 (\ce{P=O}), 3 (\ce{P-OH}), \mathbf{0 (\ce{P-H})}$ Tribasic Non-reducing

Note: Basicity = Number of $\ce{P-OH}$ bonds. Reducing character = Number of $\ce{P-H}$ bonds.

4. Group 16 (Chalcogens)

Group 16
Oxoacids of Sulfur
  • $\ce{H2SO4}$ (Sulphuric Acid): Oil of Vitriol. Manufactured via Contact Process ($\ce{V2O5}$ catalyst).
  • $\ce{H2S2O7}$ (Oleum): Pyrosulphuric acid. Contains $\ce{S-O-S}$ linkage.
  • $\ce{H2SO5}$ (Caro's Acid): Peroxymonosulphuric acid. Has one peroxy ($\ce{-O-O-}$) linkage.
  • $\ce{H2S2O8}$ (Marshall's Acid): Peroxydisulphuric acid. Has one peroxy ($\ce{-O-O-}$) linkage.
Ozone ($\ce{O3}$): Powerful oxidizing agent. Depletes in the presence of NO (emitted by supersonic jets): $\ce{NO + O3 -> NO2 + O2}$.

5. Group 17 (Halogens)

Group 17
Crucial Anomalous Trends

Electron Gain Enthalpy

$\ce{Cl > F > Br > I}$

Bond Dissoc. Enthalpy

$\ce{Cl2 > Br2 > F2 > I2}$

$\ce{F2}$ has low BDE and low EGE due to intense e-e repulsions in its small 2p orbitals.

Interhalogen Compounds ($\ce{XX'_n}$): Formed when two different halogens react. Always more reactive than pure halogens (except $\ce{F2}$) because the $\ce{X-X'}$ bond is weaker.
Geometry e.g., $\ce{ClF3}$ (T-shaped), $\ce{IF7}$ (Pentagonal bipyramidal).

6. Group 18 (Noble Gases)

Group 18
Compound Geometry (VSEPR) Hybridization
$\ce{XeF2}$ Linear (3 l.p.) $sp^3d$
$\ce{XeF4}$ Square Planar (2 l.p.) $sp^3d^2$
$\ce{XeF6}$ Distorted Octahedral (1 l.p.) $sp^3d^3$
$\ce{XeO3}$ Pyramidal (1 l.p.) $sp^3$
$\ce{XeOF4}$ Square Pyramidal (1 l.p.) $sp^3d^2$
Hydrolysis of $\ce{XeF6}$ (Highly Tested)
Complete Hydrolysis: $\ce{XeF6 + 3H2O -> XeO3 + 6HF}$
Partial Hydrolysis (1 eq water): $\ce{XeF6 + H2O -> XeOF4 + 2HF}$
Partial Hydrolysis (2 eq water): $\ce{XeF6 + 2H2O -> XeO2F2 + 4HF}$

© 2026 CHEMCA Academy. All Rights Reserved.

๐ŸŽฏ Complete Chemistry Revision Toolkit

Score higher by combining Formula Sheets, Flashcards and the Mistake Bank. These three resources help you revise faster, remember longer and avoid common exam mistakes for JEE Main, JEE Advanced, NEET and CBSE Board.

๐Ÿ’ก Best Revision Strategy: Start with Formula Sheets for quick revision, reinforce concepts using Flashcards, and finish with the Mistake Bank to avoid repeating errors in the examination.

No comments:

Post a Comment