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  2. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehydes have properties that are diverse and that depend on the remainder of the molecule. Smaller aldehydes such as formaldehyde and acetaldehyde are soluble in water, and the volatile aldehydes have pungent odors. Aldehydes can be identified by spectroscopic methods. Using IR spectroscopy, they display a strong ν CO band near 1700 cm −1.

  3. Acetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde

    Acetaldehyde (IUPAC systematic name ethanal) is an organic chemical compound with the formula CH 3 CH=O, sometimes abbreviated as MeCH=O.It is a colorless liquid or gas, boiling near room temperature.

  4. Cinnamaldehyde - Wikipedia

    en.wikipedia.org/wiki/Cinnamaldehyde

    The molecule consists of a benzene ring attached to an unsaturated aldehyde. Cinnamaldehyde is an α,β-unsaturated carbonyl compound . Its color is due to the π → π* transition: increased conjugation in comparison with acrolein shifts this band towards the visible.

  5. Propionaldehyde - Wikipedia

    en.wikipedia.org/wiki/Propionaldehyde

    Propionaldehyde exhibits the reactions characteristic of alkyl aldehydes, e.g. hydrogenation, aldol condensations, oxidations, etc. It is the simplest aldehyde with a prochiral methylene such that α-functionalized derivatives (CH 3 CH(X)CHO) are chiral.

  6. Salicylaldehyde - Wikipedia

    en.wikipedia.org/wiki/Salicylaldehyde

    Salicylaldehyde is produced by condensation of phenol with formaldehyde to give hydroxybenzyl alcohol, which is oxidized to the aldehyde. [4] Salicylaldehydes in general are prepared by ortho-selective formylation reactions from the corresponding phenol, for instance by the Duff reaction, Reimer–Tiemann reaction, or by treatment with paraformaldehyde in the presence of magnesium chloride and ...

  7. Category:Aldehydes - Wikipedia

    en.wikipedia.org/wiki/Category:Aldehydes

    An aldehyde is either a functional group consisting of a terminal carbonyl group, or a compound containing a terminal carbonyl group. (Where -R represents the carbon chain.) Subcategories

  8. Crotonaldehyde - Wikipedia

    en.wikipedia.org/wiki/Crotonaldehyde

    Properties Chemical formula. C 4 H 6 O: Molar mass: 70.091 g·mol −1 ... As an unsaturated aldehyde, crotonaldehyde is a versatile intermediate in organic synthesis.

  9. Butyraldehyde - Wikipedia

    en.wikipedia.org/wiki/Butyraldehyde

    This unsaturated aldehyde is then partially hydrogenated to form 2-ethylhexanal, a precursor to plasticizers such as bis(2-ethylhexyl) phthalate. [ 4 ] Butyraldehyde is a component in the two-step synthesis of trimethylolpropane , which is used for the production of alkyd resins .