An aldehyde is an organic compound containing a terminal carbonyl group. This functional group, called an aldehyde group, consists of a carbon atom bonded to a hydrogen atom with a single covalent bond and an oxygen atom with a double bond. Thus the chemical formula for an aldehyde functional group is -CH=O, and the general formula for an aldehyde is R-CH=O. The aldehyde group is occasionally called the formyl or methanoyl group. Other classes of organic compounds containing carbonyl groups include ketones and carboxylic acids.
The word aldehyde seems to have arisen from alcohol dehydrogenated. In the past, aldehydes were sometimes named after the corresponding alcohols, for example vinous aldehyde for acetaldehyde. (Vinous is from Latin vinum = wine, the traditional source of ethanol; compare vinyl.)
IUPAC names for aldehydes
IUPAC prescribes the following nomenclature for aldehydes:
- Acyclic aliphatic aldehydes are named as derivatives of the longest carbon chain containing the aldehyde group. Thus, HCHO is named as a derivative of methane, and CH3CH2CH2CHO is named as a derivative of butane. The name is formed by changing the suffix -e of the parent alkane to -al, so that HCHO is named methanal, and CH3CH2CH2CHO is named butanal.
- In other cases, such as when a -CHO group is attached to a ring, the suffix -carbaldehyde may be used. Thus, C6H11CHO is known as cyclohexanecarbaldehyde.
- If another functional group is present which IUPAC rules prescribe must be named as a suffix, the aldehyde group is named with the prefix formyl-. This prefix is preferred to methanoyl-.
- If replacing the aldehyde group with a carboxyl (-COOH) group would yield a carboxylic acid with a trivial name, the aldehyde may be named by replacing the suffix -ic acid or -oic acid in this trivial name by -aldehyde. For example:
The carbon atom adjacent to a carbonyl group is called the α carbon. Carbon atoms further away from the group may be named β for the carbon atom bonded to the α carbon, γ for the next, and so on. Hydrogen atoms bonded to these carbon atoms are named likewise—an α hydrogen is a hydrogen atom bonded to the α carbon and so on.
A reaction that introduces an aldehyde group is known as a formylation reaction.
The H atom that is part of the -CH=O group is known as the α-hydrogen atom. This hydrogen atom is more acidic than a hydrogen atom in an alkane (with a typical pKa of 17). This property is explained in terms of what is called "resonance stabilization" of the conjugate base.
There are several methods for preparing aldehydes:
- Reacting a primary alcohol with an oxidizing agent. In the laboratory this may be achieved by heating the alcohol with a chromium(VI) reagent and acidified solution of potassium dichromate, which is reduced to green Cr3+ during the reaction. Excess dichromate will further oxidise the aldehyde to form a carboxylic acid, so either the aldehyde is distilled out as it forms (if volatile), or milder methods and reagents such as PCC oxidation, IBX acid, Dess-Martin periodinane or Swern oxidation are used. The reaction is illustrated below with propan-1-ol being oxidised to form propionaldehyde, and again with pentan-1-ol being oxidized to form pentanal.
- Reacting an alkene (if there is a vinylic hydrogen) with ozone will form an ozonide (an unstable, explosive intermediate) which yields an aldehyde upon reduction with zinc and acid at reduced temperatures. This process is called ozonolysis.
- Reacting an ester with diisobutyl aluminium hydride (DIBAL-H) or sodium aluminium hydride can cause reduction, yielding an aldehyde.
- Reduction of an acid chloride using the Rosenmund reduction or using lithium tri-t-butoxyaluminium hydride (LiAlH(O-t-C4H9)3).
- Reaction of ketones with methoxymethylenetriphenylphosphine in a modified Wittig reaction.
- Various formylation reactions, such as the Vilsmeier-Haack reaction, can be used to introduce an aldehyde group.
- In the Nef reaction, aldehydes form by hydrolysis of salts of primary nitro compounds.
- Zincke aldehydes form by reaction of pyridinium salts with secondary amines followed by hydrolysis.
- In the Stephen aldehyde synthesis aldehydes form from nitriles, tin chloride and hydrochloric acid.
Aldehydes can exist in either the keto or enol tautomers. Keto-enol tautomerism is catalyzed by either acid or base.
Reduction and oxidation
- The aldehyde group can be reduced to the group -CH2OH, changing the aldehyde into a primary alcohol.
- The aldehyde group can be oxidized to the group -COOH, yielding a carboxylic acid. Suitable oxidizing agents include potassium permanganate, nitric acid, chromium(VI) oxide, and acidified potassium dichromate.
- Another oxidation reaction is the silver mirror test. In this test, an aldehyde is treated with Tollens' reagent, which is prepared by adding a drop of sodium hydroxide solution into silver nitrate solution to give a precipitate of silver(I) oxide, and then adding just enough dilute ammonia solution to redissolve the precipitate in aqueous ammonia to produce [Ag(NH3)2]+ complex. This reagent will convert aldehydes to carboxylic acids without attacking carbon-carbon double-bonds. The name silver mirror test arises because this reaction will produce a precipitate of silver whose presence can be used to test for the presence of an aldehyde.
Nucleophilic addition reactions
In nucleophilic addition reactions a nucleophile can add to the carbon atom in the carbonyl group, yielding an addition compound where this carbon atom has tetrahedral molecular geometry. Together with protonation of the oxygen atom in the carbonyl group (which can take place either before or after addition), this yields a product where the carbon atom in the carbonyl group is bonded to the nucleophile, a hydrogen atom, and a hydroxyl group.
There are various examples of nucleophilic addition reactions.
- In the acetalisation reaction, under acidic or basic conditions, an alcohol adds to the carbonyl group and a proton is transferred to form a hemiacetal. Under acidic conditions, the hemiacetal and the alcohol can further react to form an acetal and water. Simple hemiacetals are usually unstable, although cyclic ones such as glucose can be stable. Acetals are stable, but revert to the aldehyde in the presence of acid.
- Aldehydes can react with water (under acidic or basic conditions) to form hydrates, R-C(H)(OH)(OH), although these are only stable when strong electron withdrawing groups are present, as in chloral hydrate. The mechanism is identical to hemiacetal formation.
- In alkylimino-de-oxo-bisubstitution, a primary or secondary amine adds to the carbonyl group and a proton is transferred from the nitrogen to the oxygen atom to create a carbinolamine. In the case of a primary amine, a water molecule can be eliminated from the carbinolamine to yield an imine. This reaction is catalyzed by acid.
- The cyano group in HCN can add to the carbonyl group to form cyanohydrins, R-C(H)(OH)(CN).
- In the Grignard reaction, a Grignard reagent adds to the group, eventually yielding an alcohol with a substituted group from the Grignard reagent.
- Hydroxylamine (NH2OH) can add to the carbonyl group. After the elimination of water, this will result in an oxime.
- An ammonia derivative of the form H2NNR2 such as hydrazine (H2NNH2) or 2,4-dinitrophenylhydrazine can add to the carbonyl group. After the elimination of water, this will result in the formation of a hydrazone.
More complex reactions
- If an aldehyde is converted to a simple hydrazone (RCH=NHNH2) and this is heated with a base such as KOH, the terminal carbon is fully reduced via the Wolff-Kishner reaction to a methyl group. The Wolff-Kishner reaction may be performed as a one-pot reaction, giving the overall conversion RCH=O → RCH3.
- Reaction of aldehydes with reducing agents such as magnesium gives diols in a Pinacol coupling reaction.
- The Wittig reaction takes aldehydes to alkenes and the Corey-Fuchs reaction takes aldehydes to alkynes. Both use a triphenylphosphine reagent. The Corey-Chaykovsky reagent is a sulfonium ylide which converts aldehydes to epoxides.
Examples of aldehydes
- Methanal (Formaldehyde)
- Ethanal (Acetaldehyde)
- Propionaldehyde (propanal)
- Butyraldehyde (butanal)
- McMurry, John. Organic Chemistry. 6th ed. Belmont, CA: Brooks/Cole, 2004. ISBN 0534420052
- Morrison, Robert T., and Robert N. Boyd. Organic Chemistry. 6th ed. Englewood Cliffs, NJ: Prentice Hall, 1992. ISBN 0-13-643669-2
- Solomons, T.W. Graham, and Craig B. Fryhle. Organic Chemistry. 8th ed. Hoboken, NJ: John Wiley, 2004. ISBN 0471417998
All links retrieved September 15, 2012.
- Aldehydes IUPAC Compendium of Chemical Terminology - the Gold Book.
- IUPAC Nomenclature of Organic Chemistry. International Union of Pure and Applied Chemistry.
|Chemical class: Alcohol • Aldehyde • Alkane • Alkene • Alkyne • Amide • Amine • Azo compound • Benzene derivative • Carboxylic acid • Cyanate • Ester • Ether • Haloalkane • Imine • Isocyanide • Isocyanate • Ketone • Nitrile • Nitro compound • Nitroso compound • Peroxide • Phosphoric acid • Pyridine derivative • Sulfone • Sulfonic acid • Sulfoxide • Thioether • Thiol • Toluene derivative|
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