Hofmann Rearrangement (Amide → Amine, One-Carbon Shorter): Mechanism + Exam Traps
Primary amides convert to primary amines with one fewer carbon using Br₂/NaOH (or similar).
- Reaction: Hofmann Rearrangement (Amide → Amine, One-Carbon Shorter)
- What it does: Primary amides convert to primary amines with one fewer carbon using Br₂/NaOH (or similar).
- Typical reagents: Br2, NaOH (or NaOBr)
- Key intermediate: Varies / context-dependent
- Driving force: Formation of more stable bonds / products
- Exam type: Predict product
- Exam type: Rearrangement logic
- Exam type: Driving force