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A condensation reaction is a chemical reaction in which two molecules or moieties (functional groups) combine to form one single molecule, together with the loss of a small molecule.[1] When this small molecule is water, it is known as a dehydration reaction; other possible small molecules lost are hydrogen chloride, methanol, or acetic acid.
When two separate molecules react, the condensation is termed intermolecular. A simple example is the condensation of two amino acids to form the peptide bond characteristic of proteins. This reaction example is the opposite of hydrolysis, which splits a chemical entity into two parts through the action of the polar water molecule, which itself splits into hydroxide and hydrogen ions.
If the union is between atoms or groups of the same molecule, the reaction is termed intramolecular condensation, and in many cases leads to ring formation. An example is the Dieckmann condensation, in which the two ester groups of a single diester molecule react with each other to lose a small alcohol molecule and form a β-ketoester product.
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Mechanism
Many condensation reactions follow a nucleophilic acyl substitution or an aldol condensation reaction mechanism. Other condensations, such as the acyloin condensation are triggered by radical or single electron transfer conditions.
The synthesis of polymers, where monomers react and become covalently bonded with one another through the loss of a water molecule.
Condensation reactions in polymer chemistry
In polymer chemistry, a series of condensation reactions take place whereby monomers or monomer chains add to each other to form longer chains. This may also be termed as 'condensation polymerization' or 'step-growth polymerization'. It occurs either as a homopolymerization of an A-B monomer or a polymerization of two co-monomers A-A and B-B. Small molecule condensates are usually liberated, unlike in polyaddition where there is no liberation of small molecules.
A high conversion rate is required to achieve high molecular weights as per Carothers' equation.
In general, condensation polymers form more slowly than addition polymers, often requiring heat. They are generally lower in molecular weight. Monomers are consumed early in the reaction; the terminal functional groups remain active throughout and short chains combine to form longer chains. Bifunctional monomers lead to linear chains (and therefore thermoplastic polymers), but when the monomer functionality exceeds two, the product is a thermoset polymer.
Applications
This type of reaction is used as a basis for the making of many important polymers for example: nylon, polyester and other condensation polymers and various epoxies. It is also the basis for the laboratory formation of silicates and polyphosphates. The reactions that form acid anhydrides from their constituent acids are typically condensation reactions.
Many biological transformations are condensation reactions. Polypeptide synthesis, polyketide synthesis, terpene syntheses, phosphorylation, and glycosylations are a few examples of this reaction.
A large number of such reactions are used in synthetic organic chemistry. Other examples include:
- Acyloin condensation
- Aldol condensation
- Benzoin condensation (this is not technically a condensation, but is called so for historical reasons)[1]
- Claisen condensation
- Claisen-Schmidt condensation
- Darzens condensation (glycidic ester condensation)
- Dieckmann condensation
- Guareschi-Thorpe condensation
- Knoevenagel condensation
- Michael condensation
- Pechmann condensation
- Rap-Stoermer condensation
- Self-condensation or symmetrical aldol condensation
- Ziegler condensation
See named reactions
References
- ^ a b International Union of Pure and Applied Chemistry (1994). "Condensation Reaction". Compendium of Chemical Terminology Internet edition.
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