Acetal: Difference between revisions
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[[Image:Acetal general structure.png|thumb]] |
[[Image:Acetal general structure.png|thumb]] |
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An '''acetal''' is a [[molecule]] with two single-bonded oxygen atoms attached to the same carbon atom. |
An '''acetal''' is a [[molecule]] with two single-bonded oxygen atoms attached to the same carbon atom. Yeah it is. |
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Traditional usages distinguish '''ketals''' from acetals (whereas a ketal has two carbon-bonded R groups and is formally derived from a [[ketone]], an acetal has one or both carbon-bonded R groups as a hydrogen and is formally derived from an [[aldehyde]]). Current [[IUPAC]] terminology classifies ketals as a subset of acetals.<ref>{{GoldBookRef|title=ketals|file=K03376}}</ref> |
Traditional usages distinguish '''ketals''' from acetals (whereas a ketal has two carbon-bonded R groups and is formally derived from a [[ketone]], an acetal has one or both carbon-bonded R groups as a hydrogen and is formally derived from an [[aldehyde]]). Current [[IUPAC]] terminology classifies ketals as a subset of acetals.<ref>{{GoldBookRef|title=ketals|file=K03376}}</ref> |
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Revision as of 12:59, 6 October 2011
 | It has been suggested that Acetalisation be merged into this article. (Discuss) Proposed since February 2011. |
An acetal is a molecule with two single-bonded oxygen atoms attached to the same carbon atom. Yeah it is.
Traditional usages distinguish ketals from acetals (whereas a ketal has two carbon-bonded R groups and is formally derived from a ketone, an acetal has one or both carbon-bonded R groups as a hydrogen and is formally derived from an aldehyde). Current IUPAC terminology classifies ketals as a subset of acetals.[1]
Formation of an acetal occurs when the hydroxyl group of a hemiacetal becomes protonated and is lost as water. The carbocation ion that is produced is then rapidly attacked by a molecule of alcohol. Loss of the proton from the attached alcohol gives the acetal.
Acetals are stable compared to hemiacetals but their formation is a reversible equilibrium as with esters. As a reaction to create an acetal proceeds, water must be removed from the reaction mixture, for example, with a Dean-Stark apparatus, lest it will hydrolyse the product back to the hemiacetal. The formation of acetals reduces the total number of molecules present and therefore is not favourable with regards to entropy. A way to improve this is to use an orthoester as a source of alcohol. Aldehydes and ketones undergo a process called acetal exchange with orthoesters to give acetals. Water produced along with the acetal product is used up in hydrolysing the orthoester and producing more alcohol to be used in the reaction.
Most glycosidic bonds in carbohydrates and other polysaccharides are acetal linkages.[2] Acetaldehyde diethyl acetal is an important flavouring compound in distilled beverages.[3]
The plastic known as acetal is a polyacetal of formaldehyde.
Acetals are used as protecting groups for carbonyl groups in organic synthesis as they are stable with respect to hydrolysis by bases and with respect to many oxidizing and reducing agents.
Examples
- Dimethoxymethane, a solvent
- Dioxolane
- Methylenedioxy group
- Metaldehyde
- Paraldehyde
- 1,3,5-Trioxane
References
- ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "ketals". doi:10.1351/goldbook.K03376
- ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "glycosides". doi:10.1351/goldbook.G02661
- ^ Volatile Compounds in Foods and Beverages, ISBN 0-8247-8390-5, http://books.google.com/books?id=_OvXjhLUz-oC, p.554