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How many distinct products (including stereoisomers) are formed when 3-methylpent-2-ene reacts with Br₂ in CCl₄ under dark conditions? ms chauhan organic chemistry advanced problems pdf
| Column I (Reaction) | Column II (Mechanism type) | |---------------------|----------------------------| | 1. Sandmeyer reaction | A. Electrophilic substitution | | 2. Fries rearrangement | B. Free radical | | 3. Hunsdiecker reaction | C. Nucleophilic aromatic substitution | | 4. Chichibabin reaction | D. Single electron transfer | I understand you're looking for a document related