Because the elements of group 4 have a high affinity for oxygen, all three metals occur naturally as oxide ores that contain the metal in the +4 oxidation state resulting from losing all four ns2(n − 1)d2 valence electrons. They are isolated by initial conversion to the tetrachlorides, as shown for Ti:



followed by reduction of the tetrachlorides with an active metal such as Mg.

The chemistry of the group 4 metals is dominated by the +4 oxidation state. Only Ti has an extensive chemistry in lower oxidation states.

In contrast to the elements of group 3, the group 4 elements have important applications. Titanium (melting point = 1668°C) is often used as a replacement for aluminum (melting point = 660°C) in applications that require high temperatures or corrosion resistance. For example, friction with the air heats the skin of supersonic aircraft operating above Mach 2.2 to temperatures near the melting point of aluminum; consequently, titanium is used instead of aluminum in many aerospace applications. The corrosion resistance of titanium is increasingly exploited in architectural applications, as shown in the chapter-opening photo. Metallic zirconium is used in UO2-containing fuel rods in nuclear reactors, while hafnium is used in the control rods that modulate the output of high-power nuclear reactors, such as those in nuclear submarines.

Table below shows Some Properties of the Elements of Groups 4
Element Z Valence Electron Configuration Electronegativity Metallic Radius (pm) Melting Point (°C) Density (g/cm3)
Ti 22 4s23d2 1.54 147 1668 4.51
Zr 40 5s24d2 1.33 160 1855 6.52
Hf 72 6s25d24f14 1.30 159 2233 13.31

Consistent with the periodic trends, the group 4 metals become denser, higher melting, and more electropositive down the column (Table 1

1). Unexpectedly, however, the atomic radius of Hf is slightly smaller than that of Zr due to the lanthanide contraction. Because of their ns2(n − 1)d2 valence electron configurations, the +4 oxidation state is by far the most important for all three metals. Only titanium exhibits a significant chemistry in the +2 and +3 oxidation states, although compounds of Ti2+ are usually powerful reductants. In fact, the Ti2+(aq) ion is such a strong reductant that it rapidly reduces water to form hydrogen gas.

Reaction of the group 4 metals with excess halogen forms the corresponding tetrahalides (MX4), although titanium, the lightest element in the group, also forms dihalides and trihalides (X is not F). The covalent character of the titanium halides increases as the oxidation state of the metal increases because of increasing polarization of the anions by the cation as its charge-to-radius ratio increases. Thus TiCl2 is an ionic salt, whereas TiCl4 is a volatile liquid that contains tetrahedral molecules. All three metals react with excess oxygen or the heavier chalcogens (Y) to form the corresponding dioxides (MO2) and dichalcogenides (MY2). Industrially, TiO2, which is used as a white pigment in paints, is prepared by reacting TiCl4 with oxygen at high temperatures:



The group 4 dichalcogenides have unusual layered structures with no M–Y bonds holding adjacent sheets together, which makes them similar in some ways to graphite. The group 4 metals also react with hydrogen, nitrogen, carbon, and boron to form hydrides (such as TiH2), nitrides (such as TiN), carbides (such as TiC), and borides (such as TiB2), all of which are hard, high-melting solids. Many of these binary compounds are nonstoichiometric and exhibit metallic conductivity.

The Layered Structure of TiS2. Each titanium atom is surrounded by an octahedral arrangement of six sulfur atoms that are shared to form extended layers of atoms. Because the layers are held together by only van der Waals forces between adjacent sulfur atoms, rather than covalent bonds, the layers slide past one another relatively easily when a mechanical stress is applied.


  • a) CO2 – molecular
  • b) SiO2 – macromolecular
  • c) GeO2, SnO2, PbO2 – intermediate between ionic and macomolecular


  • a) CO2 and SiO2 are acid and react with alkalis to form salts.

CO2(g) + 2NaOH(aq) → Na2CO3(aq) + H2O(l)

  • b) GeO, SnO2 and PbO2 are amphoteric and will react with both acids and alkalis.

SnO2(s) + conc.HCl(l) → SnCl4(l) + 2H2O(l)

SnO2(s) + 2OH(aq) → SnO32-(aq) + H2O(l)

Thermal stability

They are very stable to high temperature except PbO2 which readily loses O2.

2PbO2(s) → 2PbO(s) + O2(g)

Monoxides (Oxidation State +2)


  • a) CO and SiO are molecular. CO has a lone pair of electrons hence, can act as a ligand forming complexes with transition metals. For example: Ni(CO)42+
  • b) GeO, SnO, PbO are mainly ionic.


  • a) CO and SiO are neutral and react neither with acids or alkalis.
  • b) GeO, SnO, PbO are amphoteric.

SnO(s) + 2HCl(aq) → SnCl2(aq) + H2O(l)

SnO(s) + 2OH(aq) → [Sn(H204)4]2-(aq)

Thermal stability

The only stable one is PbO. The others are readily oxidised on standing in air to the dioxide.




Welcome to FAWE

STEM Elearning

We at FAWE have built this platform to aid learners, trainers and mentors get practical help with content, an interactive platform and tools to power their teaching and learning of STEM subjects, more

How to find your voice as a woman in Africa

© FAWE, Powered by: Yaaka DN.