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  2. Ethanol - Wikipedia

    en.wikipedia.org/wiki/Ethanol

    Ethanol (also called ethyl alcohol, grain alcohol, drinking alcohol, or simply alcohol) is an organic compound with the chemical formula CH 3 CH 2 OH.It is an alcohol, with its formula also written as C 2 H 5 OH, C 2 H 6 O or EtOH, where Et stands for ethyl.

  3. File:Ethanol-3d-stick-structure.svg - Wikipedia

    en.wikipedia.org/wiki/File:Ethanol-3d-stick...

    The following other wikis use this file: Usage on ca.wikipedia.org Bioetanol; Usage on ckb.wikipedia.org سووتەمەنی ئیسانۆل; سوتەمەنی ئیسانۆل

  4. Crotonaldehyde - Wikipedia

    en.wikipedia.org/wiki/Crotonaldehyde

    2 CH 3 CHO → CH 3 CH=CHCHO + H 2 O. Crotonaldehyde is a multifunctional molecule that exhibits diverse reactivity. It is a prochiral dienophile. [5] It is a Michael acceptor. Addition of methylmagnesium chloride produces 3-penten-2-ol. [6]

  5. 4-Heptanone - Wikipedia

    en.wikipedia.org/wiki/4-Heptanone

    [2] Butyrone is used in the synthesis of 3-propylthio-4-heptanol [1838-73-9], [ 3 ] which has found use as a flavor augmenting or enhancing composition in foodstuffs. References

  6. Ethyl octanoate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_octanoate

    Ethyl octanoate, also known as ethyl caprylate, is a fatty acid ester formed from caprylic acid and ethanol.A colorless liquid at room temperature, it has the semi-developed formula of CH 3 (CH 2) 6 COOCH 2 CH 3, and is used in food industries as a flavoring and in the perfume industry as a scent additive.

  7. Isobutanol - Wikipedia

    en.wikipedia.org/wiki/Isobutanol

    Isobutanol (IUPAC nomenclature: 2-methylpropan-1-ol) is an organic compound with the formula (CH 3) 2 CHCH 2 OH (sometimes represented as i-BuOH).This colorless, flammable liquid with a characteristic smell is mainly used as a solvent either directly or as its esters.

  8. 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 ...

  9. Koch reaction - Wikipedia

    en.wikipedia.org/wiki/Koch_reaction

    The Koch reaction is an organic reaction for the synthesis of tertiary carboxylic acids from alcohols or alkenes and carbon monoxide.Some commonly industrially produced Koch acids include pivalic acid, 2,2-dimethylbutyric acid and 2,2-dimethylpentanoic acid. [1]