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| A '''condensation reaction''' (also known as a ] or '''dehydration synthesis''' when water is lost) is a ] in which two ]s or ] react and become ]ly bonded to one another by the concurrent loss of a small molecule, often ], ], or a type of hydrogen halide such as ]. It may be considered as the opposite of a ] reaction (the cleavage of a chemical entity into two parts by the action of water). | |||
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| ==Mechanism== | |||
| Many condensation reactions follow a ] or an ] ]. Other condensations, such as the ] are triggered by ] or ] 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 ]. | |||
| 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 ]s for example: ], ] and other ]s and various ]. It is also the basis for the laboratory formation of ]s and ]s. The reactions that form acid ]s from their constituent acids are typically condensation reactions. Other organic condensation reactions are ]s, ], the ] and the ]. | |||
| Nearly all biological transformations are condensation reactions. Polypeptide synthesis, polyketide synthesis, terpene syntheses, phosphorylation, glycosylations, are just a few examples. | |||
| ]s to form a ].]] | |||
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Revision as of 02:29, 1 December 2006
A condensation reaction (also known as a dehydration reaction or dehydration synthesis when water is lost) is a chemical reaction in which two molecules or moieties react and become covalently bonded to one another by the concurrent loss of a small molecule, often water, methanol, or a type of hydrogen halide such as HCl. It may be considered as the opposite of a hydrolysis reaction (the cleavage of a chemical entity into two parts by the action of water).
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 Carother's 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. Other organic condensation reactions are Aldol condensations, self-condensation, the acyloin condensation and the benzoin condensation.
Nearly all biological transformations are condensation reactions. Polypeptide synthesis, polyketide synthesis, terpene syntheses, phosphorylation, glycosylations, are just a few examples.
