A chemist needs to reduce a keto-group to a CH2 group in a molecule containing an acid-sensitive acetal linkage. Which method must be avoided?
Q1. A chemist needs to reduce a keto-group to a CH2 group in a molecule containing an acid-sensitive acetal linkage. Which method must be avoided?
Answer: Clemmensen reduction
Explanation: Clemmensen reduction uses acidic Zn-Hg/HCl, while Wolff-Kishner uses basic NH2NH2/KOH, making Clemmensen unsuitable for acid-sensitive molecules.