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  2. Ozonolysis - Wikipedia

    en.wikipedia.org/wiki/Ozonolysis

    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. Erucic acid is a precursor to brassylic acid, a C13-dicarboxylic acid that is used to make specialty polyamides and polyesters. The conversion entails ozonolysis, which selectively cleaves the C=C bond in erucic acid: [21]

  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. 3-Methyl-3-penten-2-one - Wikipedia

    en.wikipedia.org/wiki/3-Methyl-3-penten-2-one

    3-Methyl-3-penten-2-one is an unsaturated aliphatic ketone. It is an isomer of mesityl oxide and isomesityl oxide. It is a precursor of 3-methyl-2-pentanone (methyl sec-butyl ketone) and is obtained by acid-catalyzed dehydration of 4-hydroxy-3-methyl-2-pentanone. It is used as an intermediate in organic chemistry syntheses. [1]

  5. Olefin metathesis - Wikipedia

    en.wikipedia.org/wiki/Olefin_metathesis

    But by tweaking this structure to a PR 3 Ta(CHt−bu)(Ot−bu) 2 Cl (replacing chloride by t-butoxide and a cyclopentadienyl by an organophosphine, metathesis was established with cis-2-pentene. [45] In another development, certain tungsten oxo complexes of the type W(O)(CHt−Bu)(Cl) 2 (PEt) 3 were also found to be effective. [46]

  6. Griesbaum coozonolysis - Wikipedia

    en.wikipedia.org/wiki/Griesbaum_coozonolysis

    The oxime first reacts with the ozone to form the corresponding carbonyl oxide, undergoes 1,3-dipolar cycloaddition with the carbonyl reactant to form the cyclic ozonide, as usual for the Criegee intermediate in the ozonolysis of alkenes. If no carbonyl compound is used, the carbonyl oxide may dimerize and form 1,2,4,5-tetraoxanes.

  7. Large meals after 5 pm could contribute to type 2 diabetes risk

    www.aol.com/large-meals-5-pm-could-140000242.html

    Consuming more than 45% of daily calories after 5 p.m. can contribute to greater risk of type 2 diabetes, cardiovascular problems, and chronic inflammation, a recent study suggests.

  8. Elon Musk, Vivek Ramaswamy to meet with House ... - AOL

    www.aol.com/elon-musk-vivek-ramaswamy-meet...

    Businessmen Elon Musk and Vivek Ramaswamy will meet with House Republicans this week to discuss cuts to federal government spending, among other matters.

  9. Pentene - Wikipedia

    en.wikipedia.org/wiki/Pentene

    The branched isomers are 2-methylbut-1-ene, 3-methylbut-1-ene (isopentene), and 2-methylbut-2-ene (isoamylene). Isoamylene is one of the three main byproducts of deep catalytic cracking (DCC), which is very similar to the operation of fluid catalytic cracking (FCC).