Everything about Double Replacement Reaction totally explained
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. 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, these were formerly referred to as
double displacement or
double replacement reactions, though these terms are now discouraged.
Types of reaction
Neutralization
A
neutralization reaction is a specific type of double displacement reaction. Neutralization occurs when an
acid reacts with an equal amount of a
base. A neutralization reaction creates a solution of
salt and
water; for example:
» HCl(aq) +
NaOH(aq) →
NaCl(aq) + H
2O(l)
Aqueous metathesis
Metathesis reactions can occur between two
inorganic salts when one product is
insoluble in water, driving the reaction forward, as in the following examples:
» AgNO3(
aq) +
NaCl(aq) →
AgCl(
s) +
NaNO3(aq)
2
AgNO3(aq) +
CaCl2(aq) → 2
AgCl(s) + Ca(NO
3)
2(aq)
One of the compounds formed is usually a
precipitate, an insoluble
gas that bubbles out of the solution or an insoluble
solid, or a
molecular compound, usually
water. Since one of these conditions must always be met, a
solubility chart (or general knowledge of solubility rules) can be used in advance to predict whether two aqueous reactants will react or not.
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
carbon dioxide and
water. An example below is the common, science-fair "volcano" reaction -
acetic acid with
sodium bicarbonate:
» CH
3COOH (aq) + NaHCO
3(s) → CH
3COONa(aq) + CO
2(g) + H
2O(l)
Olefin metathesis
An important and influential reaction within
organic chemistry, which involves the principle of metathesis is the olefin metathesis reaction developed by
Yves Chauvin,
Richard R. Schrock and
Robert H. Grubbs, who shared a
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
alkylidene under the presence of catalytic metals, such as
ruthenium,
nickel, or
tungsten. It has several commercially significant applications, and it's 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.
Further Information
Get more info on 'Double Replacement Reaction'.
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