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  2. Ozonolysis - Wikipedia

    en.wikipedia.org/wiki/Ozonolysis

    The main use of ozonolysis is for the conversion of unsaturated fatty acids to value-added derivatives. Ozonolysis of oleic acid is an important route to azelaic acid. The coproduct is nonanoic acid: [20] CH 3 (CH 2) 7 CH=CH(CH 2) 7 CO 2 H} + 4 O 3 → HO 2 C(CH 2) 7 CO 2 H} + CH 3 (CH 2) 7 CO 2 H

  3. Methylpentene - Wikipedia

    en.wikipedia.org/wiki/Methylpentene

    Methylpentene is an alkene with a molecular formula C 6 H 12.The prefix "methyl-" is derived from the fact that there is a methyl(CH 3) branch, the word root "-pent-" is derived from the fact that there are 5 carbon atoms in the parent chain, while the "-ene" suffix denotes that there is a double bond present, as per IUPAC nomenclature. [1]

  4. (2R)-2-Methylpent-4-enoic acid - Wikipedia

    en.wikipedia.org/wiki/(2R)-2-Methylpent-4-enoic_acid

    R)-2-Methylpent-4-enoic acid can also be used in synthesis of other chiral compounds. For example, it has been used in the process of synthesizing the drug Sacubitril as a reagent for adding a chiral center to the molecule. [2]

  5. Pentene - Wikipedia

    en.wikipedia.org/wiki/Pentene

    Pentenes are alkenes with the chemical formula C 5 H 10.Each molecule contains one double bond within its molecular structure. Six different compounds are in this class, differing from each other by whether the carbon atoms are attached linearly or in a branched structure and whether the double bond has a cis or trans form.

  6. Griesbaum coozonolysis - Wikipedia

    en.wikipedia.org/wiki/Griesbaum_coozonolysis

    The Griesbaum coozonolysis is a name reaction in organic chemistry that allows for the preparation of tetrasubstituted ozonides (1,2,4-trioxolanes) by the reaction of O-methyl oximes with a carbonyl compound in the presence of ozone.

  7. 2-Methylpentane - Wikipedia

    en.wikipedia.org/wiki/2-Methylpentane

    As of early 1990s, it was present in American [4] and European [5] gasoline in small amounts, and by 2011 its share in US gas varied between 2 and 8%. [6] Using a quantitative structure-activity relationship (QSAR) prediction model, 2-Methylpentane has a research octane number (RON) of 75, motor octane number (MON) of 77, and cetane number (CN ...

  8. Ozonide - Wikipedia

    en.wikipedia.org/wiki/Ozonide

    Inorganic ozonides [1] are dark red salts. The anion has the bent shape of the ozone molecule.. Inorganic ozonides are formed by burning potassium, rubidium, or caesium in ozone, or by treating the alkali metal hydroxide with ozone; this yields potassium ozonide, rubidium ozonide, and caesium ozonide respectively.

  9. 2-Pentyne - Wikipedia

    en.wikipedia.org/wiki/2-Pentyne

    2-Pentyne, an organic compound ... NIST Chemistry WebBook page for 2-pentyne This page was last edited on 24 November 2023 ... Toggle the table of contents. 2-Pentyne.

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