Clemmensen Reduction: Carbonyl → Methylene (Acidic Conditions)
Learn the Clemmensen reduction: reducing aldehydes/ketones to alkanes under strongly acidic conditions. When to choose Clemmensen vs Wolff–Kishner.
- Reaction: Aldehyde/ketone → alkane
- What it does: Deletes the carbonyl oxygen (C=O → CH2)
- Typical reagents: Zn(Hg), HCl (acidic)
- Key intermediate: Surface/metal-mediated (not usually arrow-pushed in full detail in Orgo)
- Driving force: Net reduction; formation of C–H bonds
- Exam type: Reagent selection
- Exam type: Transformations