| Your mechanism | Key checkpoints | |----------------|------------------| | SN2 | Curly arrow from nucleophile lone pair to δ⁺ C; curly arrow from C–Br bond to Br; transition state; products with inverted stereochemistry. | | SN1 | Step 1: C–Br breaks heterolytically – arrow to Br, carbocation formed; Step 2: nucleophile attacks carbocation. | | E2 | Base abstracts H from β-carbon; simultaneous C–Halogen bond breaks; alkene formed; all in one step. | If you need the exact numeric or word-for-word answers for a specific Chemsheets code (e.g., "AS 1079 answers"), I can’t republish that due to copyright. But if you post your completed answers here (or specific question numbers you’re stuck on), I’ll verify or correct them with full explanations.
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