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  2. Propylene - Wikipedia

    en.wikipedia.org/wiki/Propylene

    Propylene, also known as propene, is an unsaturated organic compound with the chemical formula CH 3 CH=CH 2.It has one double bond, and is the second simplest member of the alkene class of hydrocarbons.

  3. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    In chemistry, halogenation is a chemical reaction which introduces one or more halogens into a chemical compound. Halide-containing compounds are pervasive, making this type of transformation important, e.g. in the production of polymers, drugs. [1]

  4. Markovnikov's rule - Wikipedia

    en.wikipedia.org/wiki/Markovnikov's_rule

    The rule states that with the addition of a protic acid HX or other polar reagent to an asymmetric alkene, the acid hydrogen (H) or electropositive part gets attached to the carbon with more hydrogen substituents, and the halide (X) group or electronegative part gets attached to the carbon with more alkyl substituents.

  5. 2-Methylbutanoic acid - Wikipedia

    en.wikipedia.org/wiki/2-Methylbutanoic_acid

    2-Methylbutanoic acid, also known as 2-methylbutyric acid is a branched-chain alkyl carboxylic acid with the chemical formula CH 3 CH 2 CH(CH 3)CO 2 H, classified as a short-chain fatty acid.

  6. Cyclobutane - Wikipedia

    en.wikipedia.org/wiki/Cyclobutane

    Cyclobutane is a cycloalkane and organic compound with the formula (CH 2) 4.Cyclobutane is a colourless gas and is commercially available as a liquefied gas.Derivatives of cyclobutane are called cyclobutanes.

  7. Cis-trans isomerase - Wikipedia

    en.wikipedia.org/wiki/Cis-trans_isomerase

    This enzyme -related article is a stub. You can help Wikipedia by expanding it.

  8. Nisinic acid - Wikipedia

    en.wikipedia.org/wiki/Nisinic_acid

    Nisinic acid is a very long chain polyunsaturated omega-3 fatty acid, similar to docosahexaenoic acid (DHA). The lipid name is 24:6 (n-3) and the chemical name is all-cis-6,9,12,15,18,21-tetracosahexaenoic acid.

  9. 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 ...