1-Ethyl-2-methyl-cyclopent-1-ene plus 1) O3, -78 °C; 2) (CH3)2S yields O Heptanoic acid and CO2 Pentanone and propanal Butanoic acid Pentanoic acid and propanoic acid Octan-2,6-dione
1-Ethyl-2-methyl-cyclopent-1-ene plus 1) O3, -78 °C; 2) (CH3)2S yields O Heptanoic acid and CO2 Pentanone and propanal Butanoic acid Pentanoic acid and propanoic acid Octan-2,6-dione
Chapter22: Carbonyl Alpha-substitution Reactions
Section22.SE: Something Extra
Problem 26MP: Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium...
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