Salt metathesis reaction
A salt metathesis reaction, sometimes called a double replacement reaction, double displacement reaction, or double decomposition reaction, is a chemical process involving the exchange of bonds between two non-reacting chemical species which results in the creation of products with similar or identical bonding affiliations. This reaction is represented by the general scheme:
- A-B + C-D → A-D + C-B
In older literature, the term double decomposition is frequently encountered. The term double decomposition is more specifically used when at least one of the substances does not dissolve in the solvent, as the ligand or ion exchange takes place in the solid state of the reactant. For example:
- AX(aq) + BY(s) → AY(aq) + BX(s).
Types of reactionsEdit
Salt metathesis is a common technique for exchanging counterions. The choice of reactants is guided by a solubility chart or lattice energy. HSAB theory can also be used to predict the products of a metathesis reaction.
- NaReO4 + N(C4H9)4Cl → N(C4H9)4[ReO4] + NaCl
The tetrabutylammonium salt precipitates from the aqueous solution. It is soluble in dichloromethane.
Salt metathesis can be conducted in nonaqueous solution, illustrated by the conversion of ferrocenium tetrafluoroborate to a more lipophilic salt containing the tetrakis(pentafluorophenyl)borate anion:
- [Fe(C5H5)2]BF4 + NaB(C6F5)4 → [Fe(C5H5)2]B(C6F5)4 + NaBF4
When the reaction is conducted in dichloromethane, the salt NaBF4 precipitates and the B(C6F5)4- salt remains in solution.
Metathesis reactions can occur between two inorganic salts when one product is insoluble in water. For example, the precipitation of silver chloride from a mixture of silver nitrate and cobalt hexammine chloride delivers the nitrate salt of the cobalt complex:
- 3 AgNO
3 + [Co(NH3)6]Cl3 → 3 AgCl + [Co(NH3)6](NO3)3
2 + 2CuCNS → Ba(CNS)
2 + 2CuOH
- (C5H5)2TiCl2 + 2 ClMgCH3 → (C5H5)2Ti(CH3)2 + 2 MgCl2
The salt product typically precipitates from the reaction solvent.
A neutralization reaction is a type of double replacement reaction. A neutralization reaction occurs when an acid reacts with an equal amount of a base. This usually creates a solution of a salt and water. For example, hydrochloric acid reacts with sodium hydroxide to produce sodium chloride and water:
- HCl + NaOH → NaCl + H
Reaction between an acid and a carbonate or bicarbonate always yields carbonic acid as a product, which spontaneously decomposes into carbon dioxide and water. The release of carbon dioxide gas from the reaction mixture drives the reaction to completion. For example, a common, science-fair "volcano" reaction involves the reaction of acetic acid with sodium bicarbonate:
3COOH + NaHCO
3 → CH
3COONa + CO
2 + H
- IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "metathesis". doi:10.1351/goldbook.M03878.
- J. R. Dilworth, W. Hussain, A. J. Hutson, C. J. Jones, F. S. Mcquillan "Tetrahalo Oxorhenate Anions" Inorganic Syntheses 1997, volume 31, pages 257–262. doi:10.1002/9780470132623.ch42
- J. Le Bras, H. Jiao, W. E. Meyer, F. Hampel and J. A. Gladysz, "Synthesis, Crystal Structure, and Reactions of the 17-Valence-Electron Rhenium Methyl Complex [(η5-C5Me5)Re(NO)(P(4-C6H4CH3)3)(CH3)]+B(3,5-C6H3(CF3)2)4−: Experimental and Computational Bonding Comparisons with 18-Electron Methyl and Methylidene Complexes", J. Organomet. Chem. 2000 volume 616, 54-66. doi:10.1016/S0022-328X(00)00531-3
- Payack, J. F.; Hughes, D. L.; Cai, D.; Cottrell, I. F.; Verhoeven, T. R. (2002). "Dimethyltitanocene". Organic Syntheses. 79: 19.CS1 maint: Multiple names: authors list (link)