Which of the following reactions correctly pair the starting alcohol and the mild oxidizing agent to — Aldehydes Ketones and Carboxylic Acids Chemistry Question
Question
Which of the following reactions correctly pair the starting alcohol and the mild oxidizing agent to yield a specific carbonyl compound without disrupting a susceptible $C=C$ double bond?
Answer: A,C,D
💡 Solution & Explanation
PCC, Oppenauer oxidation, and $MnO_2$ are specific and mild oxidants that do not attack carbon-carbon double bonds, making them ideal for oxidizing unsaturated alcohols. However, $CrO_3$ in an aqueous medium acts as a strong oxidant and will oxidize a primary alcohol completely to a carboxylic acid.
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