In chemistry, a reactivity series (or activity series) is an empirical, calculated, and structurally analytical progression of a series of metals, arranged by their "reactivity" from highest to lowest. It is used to summarize information about the reactions of metals with acids and water, double displacement reactions and the extraction of metals from their ores.
|Caesium Cs||Cs+||reacts with cold water||electrolysis|
|Magnesium Mg||Mg2+||reacts very slowly with cold water, but rapidly|
in boiling water, and very vigorously with acids
|Beryllium Be||Be2+||reacts with acids and steam|
|Titanium Ti||Ti4+||reacts with concentrated mineral acids||pyrometallurgical extraction using magnesium,|
or less commonly other alkali metals, hydrogen or calcium in the Kroll process
|Manganese Mn||Mn2+||reacts with acids; very poor reaction with steam.||smelting with coke|
|Chromium Cr||Cr3+||aluminothermic reaction|
|Iron Fe||Fe2+||smelting with coke|
|Antimony Sb||Sb3+||may react with some strong oxidizing acids||heat or physical extraction|
Going from the bottom to the top of the table the metals:
- increase in reactivity;
- lose electrons (oxidize) more readily to form positive ions;
- corrode or tarnish more readily;
- require more energy (and different methods) to be isolated from their compounds;
- become stronger reducing agents (electron donors).
There is no unique and fully consistent way to define the reactivity series, but it is common to use the three[not in citation given] types of reaction listed below, many of which can be performed in a high-school laboratory (at least as demonstrations).
Reaction with water and acids
- 2 Na (s) + 2 H2O (l) →2 NaOH (aq) + H2 (g)
Metals in the middle of the reactivity series, such as iron, will react with acids such as sulfuric acid (but not water at normal temperatures) to give hydrogen and a metal salt, such as iron(II) sulfate:
- Fe (s) + H2SO4 (l) → FeSO4 (aq) + H2 (g)
There is some ambiguity at the borderlines between the groups. Magnesium, aluminium and zinc can react with water, but the reaction is usually very slow unless the metal samples are specially prepared to remove the surface layer of oxide which protects the rest of the metal. Copper and silver will react with nitric acid; but because nitric acid is an oxidizing acid, the oxidizing agent is not the H+ ion as in normal acids, but the NO3− ion.
Single displacement reactions
- Fe (s) + CuSO4 (aq) → Cu (s) + FeSO4 (aq)
In general, a metal can displace any of the metals which are lower in the reactivity series: the higher metal reduces the ions of the lower metal. This is used in the thermite reaction for preparing small quantities of metallic iron, and in the Kroll process for preparing titanium (Ti comes at about the same level as Al in the reactivity series). For example, aluminium will reduce iron(III) oxide to iron, becoming aluminium oxide in the process:
- 2Al (s) + Fe2O3 (s) → 2Fe (s) + Al2O3 (s)
- 2 Mg (s) + TiCl4 (l) → Ti (s) + 2 MgCl2 (s)
However, other factors can come into play, such as in the preparation of metallic potassium by the reduction of potassium chloride with sodium at 850 °C. Although sodium is lower than potassium in the reactivity series, the reaction can proceed because potassium is more volatile, and is distilled off from the mixture.
- Na (g) + KCl (l) → K (g) + NaCl (l)
Comparison with standard electrode potentials
- Li > Cs > Rb > K > Ba > Sr > Na > Ca > Mg > Be > Al > H(in water) > Mn > Zn > Cr(+3) > Fe(+2) > Cd > Co > Ni > Sn > Pb > H(in acids) > Cu > Fe(+3) > Hg > Ag > Pd > Ir > Pt(+2) > Au > Pt(+4)
The positions of lithium and sodium are changed on such a series; gold and platinum are in joint position and not gold leading, although this has little practical significance as both metals are highly unreactive.
Standard electrode potentials offer a quantitative measure of the power of a reducing agent, rather than the qualitative considerations of other reactive series. However, they are only valid for standard conditions: in particular, they only apply to reactions in aqueous solution. Even with this proviso, the electrode potentials of lithium and sodium – and hence their positions in the electrochemical series – appear anomalous. The order of reactivity, as shown by the vigour of the reaction with water or the speed at which the metal surface tarnishes in air, appears to be
- potassium > sodium > lithium > alkaline earth metals,
the same as the reverse order of the (gas-phase) ionization energies. This is borne out by the extraction of metallic lithium by the electrolysis of a eutectic mixture of lithium chloride and potassium chloride: lithium metal is formed at the cathode, not potassium.
- Reactivity (chemistry), which discusses the inconsistent way that the term 'reactivity' is used in chemistry.
- Greenwood, Norman N.; Earnshaw, Alan (1984). Chemistry of the Elements. Oxford: Pergamon Press. pp. 82–87. ISBN 0-08-022057-6.
- France, Colin (2008), The Reactivity Series of Metals
- Briggs, J. G. R. (2005), Science in Focus, Chemistry for GCE 'O' Level, Pearson Education, p. 172
- Lim Eng Wah (2005), Longman Pocket Study Guide 'O' Level Science-Chemistry, Pearson Education, p. 190
- Wulsberg, Gary (2000). Inorganic Chemistry. p. 294.