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  2. Acetaldehyde (data page) - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde_(data_page)

    Liquid properties Std enthalpy change of formation, Δ f H o liquid –196.4 kJ/mol Standard molar entropy, S o liquid: 117.3 J/(mol K) Enthalpy of combustion, Δ c H o –1167 kJ/mol Heat capacity, c p: 96.21 J/(mol K) at 0 °C 89.05 J/(mol K) at 25 °C Gas properties Std enthalpy change of formation, Δ f H o gas –170.7 kJ/mol Standard ...

  3. Acetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde

    Acetaldehyde is an important precursor to pyridine derivatives, pentaerythritol, and crotonaldehyde. Urea and acetaldehyde combine to give a useful resin. Acetic anhydride reacts with acetaldehyde to give ethylidene diacetate, a precursor to vinyl acetate, which is used to produce polyvinyl acetate. [24] The global market for acetaldehyde is ...

  4. Vinyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Vinyl_alcohol

    At room temperature, acetaldehyde (H 3 CC(O)H) is more stable than vinyl alcohol (H 2 C=CHOH) by 42.7 kJ/mol. [3] Vinyl alcohol gas isomerizes to the aldehyde with a half-life of 30 min at room temperature. [1] H 2 C=CHOH → H 3 CC(O)H The industrial synthesis of acetaldehyde (Wacker process) proceeds via the intermediacy of a vinyl alcohol ...

  5. 1,1-Diethoxyethane - Wikipedia

    en.wikipedia.org/wiki/1,1-Diethoxyethane

    1,1-Diethoxyethane (acetaldehyde diethyl acetal) is a major flavoring component of distilled beverages, especially malt whisky [3] and sherry. [4] Although it is just one of many compounds containing an acetal functional group, this specific chemical is sometimes called simply acetal .

  6. Aminoacetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Aminoacetaldehyde

    Aminoacetaldehyde is the organic compound with the formula OHCCH 2 NH 2.Under the usual laboratory conditions, it is unstable, tending instead to undergo self-condensation. [1]

  7. Acetaldoxime - Wikipedia

    en.wikipedia.org/wiki/Acetaldoxime

    Acetaldoxime can be prepared by combining pure acetaldehyde and hydroxylamine under heating in the presence of a base. [3] Preparation of acetaldoxime from acetaldehyde and hydroxylamine. The use of CaO as a base in the preparation of oximes from various types of ketones and aldehydes under mild conditions also gave quantitative yields. [4]

  8. Molecular electronic transition - Wikipedia

    en.wikipedia.org/wiki/Molecular_electronic...

    The energy change associated with this transition provides information on the structure of the molecule and determines many of its properties, such as colour. The relationship between the energy involved in the electronic transition and the frequency of radiation is given by Planck's relation.

  9. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group.