Reactivity Trends of p-Block
Strictly aligned with the revised NMC Syllabus. Master the general chemical reactivity trends towards Hydrogen, Oxygen, and Halogens for Groups 15 to 18.
Module Focus: The New Syllabus Boundary
The latest NEET syllabus has removed the preparation and chemical properties of specific compounds (like $HNO_3, H_2SO_4$, and Interhalogens). Instead, examiners will test your ability to predict and compare General Trends in Chemical Reactivity. You must be able to rank hydrides, oxides, and halides by stability, acidic strength, and reducing power across periods and down groups based on bond dissociation enthalpies and Fajans' rules.
1. Reactivity towards Hydrogen (Hydrides)
All p-block elements react with hydrogen to form volatile, covalent hydrides. The central logic governing all their properties is Atomic Size. As you go down a group, the central atom gets larger, making the $E-H$ bond longer and weaker.
$NH_3, PH_3, AsH_3, SbH_3, BiH_3$
- Thermal Stability $\downarrow$
Bi-H bond is longest/weakest. - Reducing Power $\uparrow$
$BiH_3$ gives up H most easily. - Basic Strength $\downarrow$
Lone pair density is highest on tiny N atom ($NH_3$).
$H_2O, H_2S, H_2Se, H_2Te, H_2Po$
- Thermal Stability $\downarrow$
$H_2Po$ is least stable. - Acidic Character $\uparrow$
Bond weakens down group; $H^+$ released easily. ($H_2Te$ is strongest acid). - Reducing Power $\uparrow$
$H_2O$ is not reducing.
$HF, HCl, HBr, HI$
- Thermal Stability $\downarrow$
$HF$ is most stable. - Acidic Strength $\uparrow$
HI bond is longest/weakest. $HI$ is the strongest acid. - Reducing Power $\uparrow$
$HI$ is the strongest reducing agent.
Normally, boiling point increases down a group due to increasing molecular mass and stronger van der Waals forces. However, the first members ($NH_3, H_2O, HF$) are massive exceptions due to Intermolecular Hydrogen Bonding.
$PH_3 < AsH_3 < NH_3 < SbH_3 < BiH_3$
$H_2S < H_2Se < H_2Te < H_2O$
$HCl < HBr < HI < HF$
2. Reactivity towards Oxygen (Oxides)
p-Block elements form multiple oxides due to variable oxidation states. The central rule here is governed by Fajans' Rules: Higher oxidation state = more covalent = more acidic.
Electronegativity increases. Oxides change from basic $\rightarrow$ amphoteric $\rightarrow$ strongly acidic.
Metallic character increases. Acidic character of oxides decreases.
The oxide with the higher oxidation state is more acidic.
3. Reactivity towards Halogens (Halides)
Elements of Groups 15 and 16 form halides, typically $EX_3$ / $EX_5$ and $EX_2$ / $EX_4$ / $EX_6$ respectively.
- Pentahalides ($EX_5$): Are more covalent than trihalides (Fajans' rule: higher oxidation state +5 polarizes the halide anion more strongly).
- Nitrogen cannot form pentahalides ($NCl_5$) because it has no d-orbitals to expand its octet.
- Bi rarely forms $BiF_5$ due to the Inert Pair Effect making the +5 state highly unstable.
- Hexahalides are formed only with Fluorine (due to small size and high electronegativity).
- Sulfur hexafluoride ($SF_6$): Is exceptionally stable and kinetically inert. Why? Because the central Sulfur atom is completely sterically protected by the six bulky Fluorine atoms, preventing water or nucleophiles from attacking.
4. Group 18: The "Almost" Inert Gases
Noble gases were considered completely inert until Neil Bartlett synthesized the first real noble gas compound ($Xe^+[PtF_6]^-$) in 1962.
As you go down Group 18, atomic size increases, and Ionization Enthalpy decreases. The $IE$ of Xenon ($1170 \text{ kJ/mol}$) is low enough—and almost identical to that of molecular Oxygen ($O_2$)—that highly electronegative atoms can force it to share electrons.
Fluorine (F) and Oxygen (O)
Krypton forms only one known compound ($KrF_2$). Helium, Neon, and Argon form no true chemical compounds.
NEET Grand Test: p-Block Reactivity
15 High-Yield Questions testing acidic trends, boiling point anomalies, and steric inertness.
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