The oxidation of a secondary alcohol with NaOCl in acetic acid proceeds through the reaction of the alcohol with the reactive intermediate ClOH2+. Write a mechanism that shows how isopropyl alcohol is oxidized to acetone (CH3COCH3) using ClOH2+ in acetic acid (CH3COOH).
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Q3: Provide the structure of the major organic
Q4: What is the major organic product when
Q5: Which alcohol reacts most rapidly with the
Q6: Classify the reaction below as an oxidation,
Q7: Which of the following reagents is not
Q9: Classify the reaction below as an oxidation,
Q10: Classify the reaction below as an oxidation,
Q11: Which of the following reagents is the
Q12: Provide the major organic product of the
Q13: Provide the structure of the major organic
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