Question
Starting from methyl acetoacetate and any other necessary reagents, complete the most efficient three-step synthesis of the ketone, 3-benzyl-5-methylhexan-2-one, by dragging the appropriate compound(s)
Starting from methyl acetoacetate and any other necessary reagents, complete the most efficient three-step synthesis of the ketone, 3-benzyl-5-methylhexan-2-one, by dragging the appropriate compound(s) into the boxes. Only one set of reagents will fit into each box, and all compounds will not be used. Reactant ethyl acetoacetate) el Reagent 1 1. CHONA, CHOH 2. CI HO, heat NaBH4, HO Step 1 product Reagent 2 1. CHONA, CHOH 2. Step 2 product OH Reagent 3 Final product (3-benzyl-5-methylhexan-2-one) HSO4, HO, heat CI i OH 1. CHOH 2. Br (scroll down for more)
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Organic Chemistry
Authors: Graham Solomons, Craig Fryhle, Scott Snyder
11th edition
1118133579, 978-1118133576
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