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A condensation reaction is a class of an organic addition reaction that proceeds in a step-wise fashion to produce the addition product, usually in equilibrium, and a water molecule (hence the name condensation). The reaction may otherwise involve the formation of ammonia, ethanol, or acetic acid<ref>{{cite web|url=https://goldbook.iupac.org/html/C/C01238.html|title=Condensation Reaction|website=IUPAC Copendium of Chemical Terminology (Gold Book)|publisher=IUPAC|accessdate=7 December 2017}}</ref>. It is a versatile class of reactions that can occur in acidic or basic conditions or in the presence of a catalyst. This class of reactions is a vital part of life as it is essential to the formation of peptide bonds between amino acids<ref>{{Cite book|title=Fundamentals of Biochemistry|last=Voet|first=Donald|last2=Voet|first2=Judith|last3=Pratt|first3=Chriss|publisher=John Wiley & Sons, Inc.|year=2008|isbn=978-0470-12930-2|location=Hoboken, NJ|pages=88}}</ref>. A condensation reaction is a class of an organic addition reaction that proceeds in a step-wise fashion to produce the addition product, usually in equilibrium, and a water molecule (hence the name condensation). The reaction may otherwise involve the formation of ammonia, ethanol, or acetic acid<ref>{{cite web|url=https://goldbook.iupac.org/html/C/C01238.html|title=Condensation Reaction|website=IUPAC Copendium of Chemical Terminology (Gold Book)|publisher=IUPAC|accessdate=7 December 2017}}</ref>. It is a versatile class of reactions that can occur in acidic or basic conditions or in the presence of a catalyst. This class of reactions is a vital part of life as it is essential to the formation of peptide bonds between amino acids and the biosynthesis of fatty acids.<ref>{{Cite book|title=Fundamentals of Biochemistry|last=Voet|first=Donald|last2=Voet|first2=Judith|last3=Pratt|first3=Chriss|publisher=John Wiley & Sons, Inc.|year=2008|isbn=978-0470-12930-2|location=Hoboken, NJ|pages=88}}</ref>


Many variations of condensation reactions exist, common examples include the aldol condensation: Claisen Condensation, Knoevenagel Reaction and the Dieckman Condensation (intramolecular Claisen Condensation)<ref name=":0">{{cite book|title=Advanced Organic Chemistry|last1=Bruckner|first1=Reinhard|date=2002|publisher=Harcourt Academic Press|isbn=0-12-138110-2|edition=First|location=San Diego, California|pages=414-427|accessdate=8 December 2017}}</ref>. Many variations of condensation reactions exist, common examples include the ], ], ], and the ] (intramolecular Claisen Condensation).<ref name=":0">{{cite book|title=Advanced Organic Chemistry|last1=Bruckner|first1=Reinhard|date=2002|publisher=Harcourt Academic Press|isbn=0-12-138110-2|edition=First|location=San Diego, California|pages=414-427|accessdate=8 December 2017}}</ref>.
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The condensation reactios can be catalyzed, by simply adding a concentrated acid to the reaction. It effects it by acidifying the environment whereas the reaction takes place the acid thereby binds with the water molecules and speed up the process. Also, an example of the condensation reaction is the dehydration synthesis.


==See also== ==See also==

Revision as of 15:50, 28 December 2017

A condensation reaction is a class of an organic addition reaction that proceeds in a step-wise fashion to produce the addition product, usually in equilibrium, and a water molecule (hence the name condensation). The reaction may otherwise involve the formation of ammonia, ethanol, or acetic acid. It is a versatile class of reactions that can occur in acidic or basic conditions or in the presence of a catalyst. This class of reactions is a vital part of life as it is essential to the formation of peptide bonds between amino acids and the biosynthesis of fatty acids.

Many variations of condensation reactions exist, common examples include the aldol condensation, Claisen Condensation, Knoevenagel condensation, and the Dieckman condensation (intramolecular Claisen Condensation)..

Condensation reaction between two symmetrical aldehydes. The final product is formed irreversibly due to stability from the conjugation of the double bonds.

See also

References

  1. "Condensation Reaction". IUPAC Copendium of Chemical Terminology (Gold Book). IUPAC. Retrieved 7 December 2017.
  2. Voet, Donald; Voet, Judith; Pratt, Chriss (2008). Fundamentals of Biochemistry. Hoboken, NJ: John Wiley & Sons, Inc. p. 88. ISBN 978-0470-12930-2.
  3. Bruckner, Reinhard (2002). Advanced Organic Chemistry (First ed.). San Diego, California: Harcourt Academic Press. pp. 414–427. ISBN 0-12-138110-2. {{cite book}}: |access-date= requires |url= (help)
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