Concept understanding — Anomalous Behaviour of Lithium
Anomalous Behaviour of Lithium
You already know that all alkali metals sit together in Group 1 — sodium, potassium, rubidium, caesium, francium. They are famously reactive, soft, and form strongly ionic compounds. Lithium sits right at the top of that column, and you might expect it to behave just like the others. It doesn't. In several important ways, lithium acts more like magnesium (a Group 2 element) than like its own group members. That is the anomaly.
Why does this happen?
Two properties of lithium are responsible for almost everything unusual about it.
First, its size. Lithium is the smallest metal atom in the entire periodic table. Its atomic radius is about 152 pm, while sodium is already 186 pm. That tiny size means its outermost electron is held very tightly by the nucleus — the ionisation enthalpy of lithium is the highest among alkali metals.
Second, its polarising power. When lithium forms a positive ion, Li⁺, that ion is extremely small (only about 76 pm). A small, highly charged cation distorts the electron cloud of any anion it meets — this is polarisation. High polarising power pushes the bonding away from pure ionic character and toward covalent character. For lithium, this effect is strong enough to change the chemistry.
Note
The combination of small size and high polarising power is often called the diagonal relationship — lithium resembles magnesium, which sits diagonally below and to the right in the periodic table.
The precise statement
The anomalous behaviour of lithium means that lithium differs significantly from the rest of the alkali metals in several of its chemical properties, and in many of these it resembles magnesium instead. The key differences are:
Lithium forms a covalent, unstable carbonate. All other alkali metal carbonates (Na₂CO₃, K₂CO₃, etc.) are ionic, thermally stable, and do not decompose on heating. Lithium carbonate, Li₂CO₃, is much less ionic — it is partially covalent — and it decomposes on heating into lithium oxide and carbon dioxide:
Li2CO3ΔLi2O+CO2
This is exactly what magnesium carbonate does. Sodium carbonate, by contrast, can be heated red-hot without decomposing.
Lithium reacts with nitrogen to give a nitride. No other alkali metal does this. When lithium is heated in air, it combines directly with nitrogen to form lithium nitride:
6Li+N2→2Li3N
Magnesium does the same thing — it forms Mg₃N₂. Sodium and potassium simply do not react with nitrogen at all.
Lithium forms a stable oxide (Li₂O) rather than a peroxide or superoxide. Sodium gives Na₂O₂ (peroxide) when burned in air; potassium, rubidium, and caesium give superoxides (KO₂, RbO₂, CsO₂). Lithium, because of its small cation size, can only stabilise the simple oxide Li₂O. Again, magnesium gives MgO.
Lithium hydroxide is a weaker base. LiOH is moderately strong but much less basic than NaOH or KOH. It decomposes on heating to Li₂O, while the other alkali metal hydroxides do not decompose.
Lithium salts are often hydrated and soluble in organic solvents. LiCl is deliquescent and soluble in alcohol; NaCl and KCl are not. The small Li⁺ ion strongly attracts water molecules, forming hydrates like LiCl·3H₂O. …
LiF has a very high lattice enthalpy (both ions small) that hydration cannot overcome; LiCl has a lower lattice enthalpy and more covalent character, favouring solubility in both water and organic solvents. …
Both Li+ and F− are among the smallest ions in their respective groups. When two very small, highly charged ions come together, the lattice enthalpy of the resulting salt is exceptionally high. For LiF, this very high lattice enthalpy is not compensated by the hydration enthalpy released on dissolving, so the overall energetics disfavour dissolution — LiF is almost insoluble in water.
Step 2: Solubility of LiCl in water
Cl− is a much larger ion than F−, so LiCl has a considerably lower lattice enthalpy than LiF. This lower lattice enthalpy is easily overcome by the hydration enthalpy released when the ions are solvated, so LiCl is readily soluble in water.
Use two different arguments for the two solvents: for water solubility, compare lattice enthalpy (very high for LiF due to two small ions; lower for LiCl) against hydration enthalpy; for acetone (an organic solvent) solubility, invoke Faj …
Trying to explain LiCl's solubility in acetone using the same lattice-vs-hydration argument used for water — organic-solvent solubility is better explained via covalent character (Fajans' rules), not hydration enthalpy. …