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- Provide a mechanism3. Draw mechanism and predict product niwollo) ardnot abog ojs ed 1bo19 (q) 1. NaOH H. 2.Following are the steps in the industrial synthesis of glycerin. Cl₂ A (C₂H5C1) heat (A) CH₂=CHCH₂ Propene (B) OH HOCH₂CHCH₂OH 1,2,3-Propanetriol (glycerol, glycerin) Provide structures for all intermediate compounds (A-D) and describe the type of mechanism by which each is formed. P.3 O ▼ O▾ + ▾ C (C₂H₂C1O₂) *% 1 NaOH, H₂O All hydrogen atoms are implied. Apply formal charges where appropriate. Omit lone pairs and radical electrons from your answer. You do not have to consider stereochemistry. * B (C₂H5O) Ca(OH)2 heat Cl₂, H₂O D (C₂H6O₂) H₂O, HCI ChemDoodleⓇ
- Bonus: Propose a mechanism Must be perfect for any points NaOEt LOE! EtO EtO HOEIQ2. What are elimination reactions? Illustrate and describe the E2 reaction mechanism. Compare and contract elimination and substitution reactions with relevant examples.Please show mechanism and solution to this problem
