Metathesis reaction

Metathesis is a bimolecular process involving the exchange of bonds between the two reacting chemical species, which results in the creation of products with similar or identical bonding affiliations.^[1] To illustrate, consider two chemical species, AB and CD, which react to give AD and CB:

AB + CD → AD + CB

These chemical species can either be ionic or covalent. When referring to precipitation reactions between solutions of ions in inorganic chemistry, it was formerly referred to as double displacement or double replacement reactions, though these terms are now discouraged.

Types of reaction

Neutralization

A salt and water, for example:

NaCl(aq) + H₂O(l)

Aqueous metathesis

Metathesis reactions can occur between two salts when one product is insoluble in water, driving the reaction forward, as in the following examples:

NaNO₃(aq)

2AgCl(s) + Ca(NO₃)₂(aq)

One of the compounds formed is usually a HSAB theory can also be applied as a means of determining or prediction of products created from such a metathesis reaction.

Acid and carbonates

Another subcategory of this reaction type features acids reacting with carbonates/bicarbonates. These reactions always yield carbonic acid as a product, which in turn automatically decomposes into sodium bicarbonate:

CH₃COOH (aq) + NaHCO₃(s) → CH₃COONa(aq) + CO₂(g) + H₂O(l)

Olefin metathesis

Main article: olefin metathesis

An important and influential reaction within Nobel Prize in Chemistry in 2005.

The principle of olefin metathesis is that an alkene double bond is cleaved and redistributed alongside the redistribution of an tungsten. It has several commercially significant applications, and it is especially useful due to the relatively small amounts of side products and hazardous waste products.

In this context, the otherwise abstract concepts of metathesis are especially well-visualized in the unique diplomas which were crafted for King Carl XIV Gustaf to present to the three chemists who shared the Nobel Prize in 2005.

Metathesis as "dance" -- illustrated in Chauvin diploma, 2005 Nobel Prize in Chemistry
Metathesis as "dance" -- illustrated in Grubbs diploma, 2005 Nobel Prize in Chemistry
Metathesis as "dance" -- illustrated in Schrock diploma, 2005 Nobel Prize in Chemistry

Intramolecular metathesis of a diene

Ring formation occurs when a diene is used as the starting material. Any size ring is possible to make with metathesis of a diene. For example, in the presence of a metal catalyst, usually Grubbs catalyst, 4-methyl-1,7-octadiene forms 4-methylcyclohexene. When using terminal alkenes the by-product is always gaseous ethene.^[2]

References

^ International Union of Pure and Applied Chemistry, (2006). IUPAC Gold Book, Compendium of Chemical Terminology IUPAC Publications
^ Janice Gorzynski Smith. Organic Chemistry: Second Ed. 2008. pp 1016-1018.