Determine the product created under the following oxidation reaction.

• A.
• B.
• C.
• D.

Answer: (C)

Verified step by step guidance

1. Identify the functional group in the starting material. The starting material is a secondary alcohol, as indicated by the OH group attached to a carbon that is connected to two other carbon atoms.
2. Recognize the oxidizing agent. Potassium dichromate (K2Cr2O7) in the presence of sulfuric acid (H2SO4) is a strong oxidizing agent that can oxidize secondary alcohols to ketones.
3. Predict the product of the oxidation reaction. When a secondary alcohol is oxidized, the hydroxyl group (OH) is converted into a carbonyl group (C=O), resulting in the formation of a ketone.
4. Determine the structure of the ketone. The carbon that was originally bonded to the OH group will now be double-bonded to an oxygen atom, forming a carbonyl group. The rest of the carbon chain remains unchanged.
5. Verify the product structure. Ensure that the carbonyl group is correctly placed on the carbon that was originally bonded to the OH group, and that the overall carbon skeleton of the molecule is preserved.