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  2. 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 ...

  3. 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 ...

  4. 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.

  5. Acetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid

    acetyl chloride SOCl 2 acetic acid (i) Li[AlH 4], ether (ii) H 3 O + ethanol Two typical organic reactions of acetic acid Acetic acid undergoes the typical chemical reactions of a carboxylic acid. Upon treatment with a standard base, it converts to metal acetate and water. With strong bases (e.g., organolithium reagents), it can be doubly deprotonated to give LiCH 2 COOLi. Reduction of acetic ...

  6. Acetylene - Wikipedia

    en.wikipedia.org/wiki/Acetylene

    This reaction once was the dominant technology for acetaldehyde production, but it has been displaced by the Wacker process, which affords acetaldehyde by oxidation of ethylene, a cheaper feedstock. A similar situation applies to the conversion of acetylene to the valuable vinyl chloride by hydrochlorination vs the oxychlorination of ethylene.

  7. 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 ...

  8. 20 high-protein meal prep ideas that dietitians love - AOL

    www.aol.com/news/20-high-protein-meal-prep...

    “For example, a 1-cup serving of edamame pairs great with lightly salted pistachios and a handful of fresh berries to pack over 24 grams of protein and 11+ grams of dietary fiber,” she says.

  9. Acetal - Wikipedia

    en.wikipedia.org/wiki/Acetal

    Generic structure of acetals. In organic chemistry, an acetal is a functional group with the connectivity R 2 C(OR') 2.Here, the R groups can be organic fragments (a carbon atom, with arbitrary other atoms attached to that) or hydrogen, while the R' groups must be organic fragments not hydrogen.