Grade 10
Halogens, oxygen–sulfur, nitrogen–phosphorus, carbon–silicon
Compare the chemistry of groups 17–14 through their valence patterns, characteristic molecules and industrially important compounds, then relate halogen redox behavior to thermodynamics.
IntuitionA map of the nonmetals
Elements in groups 17, 16, 15 and 14 share outer-electron patterns. Moving down a group adds an electron shell, changing size, bonding and reactivity; neighboring groups still show distinct chemical families.
This article compares their representative molecular forms and compounds: halogens, oxygen and sulfur, nitrogen and phosphorus, then carbon and silicon.
SchoolValence patterns and group trends
Definition: Valence-electron pattern
Group 17: (7 valence electrons); group 16: ; group 15: ; group 14: . These patterns help explain common bonding and oxidation states, but do not by themselves determine every compound.
| Group / family | Valence pattern | Typical examples and trend |
|---|---|---|
| 17, halogens | ns²np⁵ | F₂, Cl₂, Br₂, I₂; oxidising ability generally decreases down the group. |
| 16, chalcogens | ns²np⁴ | O₂/O₃; sulfur commonly forms S₈ rings; oxidation states include −2, +4, +6. |
| 15, pnictogens | ns²np³ | N₂ is kinetically inert; phosphorus has several allotropes, including P₄ molecular forms. |
| 14, carbon family | ns²np² | C forms diverse covalent networks; Si is a semiconductor and forms SiO₂ and silicates. |
Down a group, atomic radius generally increases and electronegativity decreases. In group 17 the aqueous standard reduction potentials fall from F₂/F⁻ to I₂/I⁻, although phase, solvent and bond-energy terms all contribute.
| Element/family | Examples |
|---|---|
| Halogens | −1; Cl, Br, I also +1, +3, +5, +7; F is −1 in compounds. |
| O, S | O usually −2 (−1 in peroxides); S: −2, +4, +6. |
| N, P | −3 to +5 are common; N₂ is 0. |
| C, Si | −4 to +4; CO has C +2, CO₂ has C +4. |
SchoolRepresentative chemistry across the families
Halogens are diatomic. At room conditions F₂ is a pale-yellow gas, Cl₂ a yellow-green gas, Br₂ a red-brown liquid and I₂ a dark grey-violet solid (violet vapour). A more reactive halogen displaces a less reactive halide from solution.
Example: Halogen displacement
What forms when chlorine water is added to excess potassium bromide?
Solution
Chlorine is the stronger oxidant, so it oxidises Br⁻ to Br₂. The balanced net ionic equation is ; K⁺ is a spectator ion.
Hydrogen-halide acid strength in water increases HF < HCl < HBr < HI as the H–X bond becomes easier to break. As reducing agents, the halide ions strengthen in the order F⁻ < Cl⁻ < Br⁻ < I⁻; do not confuse acid strength with the oxidising strength of X₂.
Silver nitrate gives AgCl white, AgBr cream and AgI yellow precipitates; dilute ammonia dissolves AgCl, concentrated ammonia dissolves AgBr less readily, and AgI is insoluble. Chlorine reacts reversibly with water to form hydrochloric acid and hypochlorous acid; hypochlorous acid provides bleach action.
Oxygen has O₂ and O₃ allotropes; ozone is a reactive, protective trace gas in the stratosphere. Elemental sulfur commonly occurs as S₈ rings. Burning sulfur forms pungent SO₂; catalytic oxidation to SO₃ and absorption in concentrated sulfuric acid are central to the contact process. Concentrated H₂SO₄ is a strong acid and, depending on conditions, a dehydrating and oxidising agent. H₂S is a toxic weak acid and reducing agent.
Nitrogen gas is relatively inert because its N≡N bond is very strong. The Haber–Bosch process combines N₂ and H₂ reversibly to make NH₃; the Ostwald process oxidises NH₃ to nitric acid. NO₂ is brown and dimerises to colourless N₂O₄ more at lower temperature. White phosphorus consists of P₄ molecules and is dangerously reactive; phosphoric acid H₃PO₄ and phosphate salts are important in fertilisers.
Carbon forms CO, a colourless toxic gas that binds haemoglobin, and CO₂, a linear greenhouse gas and product of complete combustion. Silicon dioxide is a giant covalent solid; silicates built from linked SiO₄ tetrahedra dominate many rocks. Crystalline silicon is a semiconductor whose conductivity can be tuned by doping.
UndergraduateRedox potentials and bond energetics
The Frost-diagram idea plots oxidation state against standard reduction potential (often through ): the thermodynamically favored redox direction corresponds to a downhill change in free energy. For halogens, the large positive potentials make X₂ strong oxidants, with the trend F₂ > Cl₂ > Br₂ > I₂ in water.
| Couple | E° / V |
|---|---|
| +2.87 | |
| +1.36 | |
| +1.07 | |
| +0.54 |
Fluorine has an unusually weak F–F bond because the very short bond brings three lone pairs on each small atom into strong repulsion. The net standard potential also includes atomisation, electron-affinity and hydration contributions; the high hydration of F⁻ helps make exceptionally positive. Thus the weak bond helps explain, but alone does not determine, fluorine’s oxidising strength.
UndergraduateQuantitative stoichiometry in the sulfur cycle
Example: Sulfur converted to sulfuric acid
Assuming complete conversion, how many moles of H₂SO₄ can be made from 3.20 g of sulfur?
Solution
The net atom balance gives 1 mol S per 1 mol H₂SO₄. With , , so the theoretical amount is (about 0.100 mol). Industrial yield and absorption conditions are not included.
UndergraduateOxidation-state bookkeeping
Oxidation states are formal electron-bookkeeping assignments, not literal charges in covalent molecules. In the Ostwald first step N changes from −3 in NH₃ to +2 in NO, while O changes from 0 in O₂ to −2; later oxidation of NO gives NO₂, followed by absorption and reactions that produce nitric acid.
References
- Inorganic Chemistry, 5th edition · Catherine E. Housecroft and Alan G. Sharpe, 2018
- Chemistry of the Elements, 2nd edition · N. N. Greenwood and A. Earnshaw, 1997