1) Predict the products of the following reactions (hint: in each reaction, LDA reacts with all of the reactant in the first step, leaving no leftover ketone to act as an electrophile): i) ii) i) ii) ii) H,0* 2) Predict the products of the following reactions (hint: in each reaction, the base reacts with some of the reactants, leaving plenty of leftover unreacted reactant to act as an electrophile.. note that I won't draw two copies of the reactant on homework or evaluations): NaOH heat
1) Predict the products of the following reactions (hint: in each reaction, LDA reacts with all of the reactant in the first step, leaving no leftover ketone to act as an electrophile): i) ii) i) ii) ii) H,0* 2) Predict the products of the following reactions (hint: in each reaction, the base reacts with some of the reactants, leaving plenty of leftover unreacted reactant to act as an electrophile.. note that I won't draw two copies of the reactant on homework or evaluations): NaOH heat
Chapter29: The Organic Chemistry Of Metabolic Pathways
Section29.SE: Something Extra
Problem 31MP
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In these given reactions, mentioned bases play crucial role for formation of the most stabilised intermediate such as enolate.
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