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]s to form a ] (red) with expulsion of water (blue)]]
A '''condensation reaction''', also commonly referred to as dehydration synthesis, is a ] in which two ]s or moieties (]) combine to form a larger molecule, together with the loss of a small molecule.<ref name="Gold">{{GoldBookRef|title=Condensation Reaction|file=C01238|year=1994}}</ref> Possible small molecules lost are ], ], ], or ] but most commonly in a biological reaction it is ]. The word "condensation" suggests a process in which two or more things are brought "together" (Latin "con") to form something "dense", like in condensation from gaseous to liquid state of matter; this does not imply, however, that condensation reaction products have greater density than reactants.

When two separate molecules react, the condensation is termed ]. A simple example is the condensation of two ]s to form the ] characteristic of ]. This reaction example is the opposite of ], which splits a chemical entity into two parts through the action of the polar water molecule, which itself splits into ] and ] ions. Hence energy is released.

If the union is between atoms or groups of the same molecule, the reaction is termed ] condensation, and in many cases leads to ring formation. An example is the ], in which the two ] groups of a single diester molecule react with each other to lose a small ] molecule and form a β-ketoester product.

]

==Mechanism==
Many condensation reactions follow a ] or an ] ]. Other condensations, such as the ] are triggered by ] or ] conditions.

==Condensation reactions in polymer chemistry==
In one type of polymerization reaction, a series of condensation steps take place whereby ]s or monomer chains add to each other to form longer chains. This is termed 'condensation polymerization' or ']', and occurs for example in the synthesis of ]s or ]s. It may be either a homopolymerization of a single monomer A-B with two different end groups that condense or a ]ization of two co-monomers A-A and B-B. Small molecules are usually liberated in these condensation steps, in contrast to ] reactions with no liberation of small molecules.

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. A high conversion rate is required to achieve high molecular weights as per ].

Bifunctional monomers lead to linear chains (and therefore ] polymers), but, when the monomer ] exceeds two, the product is a ] chain that may yield a ] 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.

Many biological transformations are condensation reactions. ], ] synthesis, ] syntheses, ], and ]s are a few examples of this reaction.

A large number of such reactions are used in synthetic organic chemistry. Other examples include:

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*]
*] (this is not technically a condensation, but is called so for historical reasons)<ref name="Gold"/>
*]
*]
*] (glycidic ester condensation)
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*] or symmetrical aldol condensation
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See ]

==See also==
* ]
* ]
* ]s

==References==
{{Reflist}}

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Revision as of 10:19, 3 November 2014

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