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Aldehydes
Functional groups
Articles needing additional references from December 2007

Summary Of: Aldehyde

The aldehyde group is also called the... in an aldehyde is more acidic than a hydrogen atom in an alkane... the aldehyde group is named with the prefix... If replacing the aldehyde group with a carboxyl... the aldehyde may be named by replacing the suffix... A reaction that introduces an aldehyde group is known as a... will further oxidise the aldehyde to form a... which yields an aldehyde upon reduction with zinc and acid at reduced temperatures... The aldehyde group can be reduced to the group... The aldehyde group can be oxidized to the group... will convert the aldehyde to a methyl... an aldehyde is treated with... If the aldehyde can not form an enolate... but revert to the aldehyde in the presence of acid... If an aldehyde is converted to a simple hydrazone...

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An aldehyde.-R is the group attached to the aldehyde group. | | carbonyl group | functional group | carbon | hydrogen | double-bonded | oxygen | alcohols | acetaldehyde | Latin | ethanol | vinyl | polar | Oxygen | electronegative | carbon-oxygen bond | α-hydrogen | pKa | Examples of IUPAC nomenclature for aldehydes. | IUPAC | aliphatic | alkane | methanal | butanal | formaldehyde | acetaldehyde | formylation reaction | primary alcohol | oxidizing agent | potassium dichromate | reduced | dichromate | carboxylic acid | distilled | volatile | PCC | IBX acid | Dess-Martin periodinane | Swern oxidation | propan-1-ol | propionaldehyde | pentan-1-ol | pentanal | Image:Oxidation of pentan-1-ol to pentanal.svg | alkene | vinylic | ozone | ozonolysis | ester | DIBAL-H | acid chloride | Rosenmund reduction | methoxymethylenetriphenylphosphine | Wittig reaction | formylation reactions | Vilsmeier-Haack reaction | Nef reaction | Zincke aldehydes | Stephen aldehyde synthesis | nitriles | tin(II) chloride | hydrochloric acid | Meyers synthesis | McFadyen-Stevens reaction | enol | tautomers | Keto-enol tautomerism | primary alcohol | carboxylic acid | potassium permanganate | nitric acid | chromium(VI) oxide | acidified | potassium dichromate | manganese dioxide | acetic acid | methanol | ester | Tollens' reagent | sodium hydroxide | silver nitrate | ammonia | Cannizzaro reaction | nucleophile | tetrahedral molecular geometry | addition | elimination | addition | condensation reaction | acetalisation | acidic | basic | alcohol | hemiacetal | acidic | acetal | glucose | hydrates | electron withdrawing groups | chloral hydrate | alkylimino-de-oxo-bisubstitution | imine | HCN | cyanohydrins | Grignard reaction | Grignard reagent | Barbier reaction | Nozaki-Hiyama-Kishi reaction | aldol reaction | enolates | ketones | esters | amides | carboxylic acids | aldols | aldol condensation | Hydroxylamine | oxime | ammonia | hydrazine | 2,4-dinitrophenylhydrazine | hydrazone | ketones | KOH | methyl | one-pot reaction | reducing agents | magnesium | diols | Pinacol coupling reaction | Wittig reaction | alkenes | Corey-Fuchs reaction | alkynes | triphenylphosphine | Takai reaction | Corey-Chaykovsky reagent | sulfonium ylide | epoxides | Methanal | Ethanal | Propanal | Butanal | Glucose | Cinnamaldehyde | Tolualdehyde | carbonyl groups | Ketones | Carboxylic acids | Amides | | citations | verification | reliable references | challenged | August 4 | 2007 | Elias J. Corey | J. Am. Chem. Soc. | doi | | Wiktionary | v | d | Functional groups | Chemical class | Alcohol | Alkane | Alkene | Alkyne | Amide | Amine | Azo compound | Benzene derivative | Carboxylic acid | Cyanate | Disulfide | Ester | Ether | Haloalkane | Hydrazone | Imine | Isocyanide | Isocyanate | Ketone | Oxime | Nitrile | Nitro compound | Nitroso compound | Peroxide | Phosphoric acid | Pyridine derivative | Sulfone | Sulfonic acid | Sulfoxide | Thioester | Thioether | Thiol | Categories | Aldehydes | Functional groups | Articles needing additional references from December 2007 |
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Aldehyde".