Select the suitable reagent(s) for the second step. dilute H2SO4 O conc. H2SO4, heat O RCO3H O NaOMe ○ H2, Pt The strategy of using an alkene intermediate in a two-step process to convert one functional group into another (called a functional group interconversion) can apply to a wide variety of transformations. Identify the reagents you would use to accomplish the following functional group interconversion: OH The transformation above can be performed with a two-step synthesis. Select the suitable reagent(s) for the first step. O t-BuOK ○ NaOMe ○ TsCl, pyridine O conc. H2SO4, heat O dilute H2SO4
Select the suitable reagent(s) for the second step. dilute H2SO4 O conc. H2SO4, heat O RCO3H O NaOMe ○ H2, Pt The strategy of using an alkene intermediate in a two-step process to convert one functional group into another (called a functional group interconversion) can apply to a wide variety of transformations. Identify the reagents you would use to accomplish the following functional group interconversion: OH The transformation above can be performed with a two-step synthesis. Select the suitable reagent(s) for the first step. O t-BuOK ○ NaOMe ○ TsCl, pyridine O conc. H2SO4, heat O dilute H2SO4
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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