Draw a detailed mechanism showing the formation of the product, be sure to draw all intermediate and show the movement of electros by arrows. H H 艾 火 H Br + H-Br hv + Br2
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- Draw a detailed mechanism showing the formation of all products, be sure to draw all intermediate and show the movement of electros by arrows. CH3 CH3 CH;OH Br OCH3 НeatConsider the intramolecular nucleophilic substitution reaction shown here. Does the stereochemistry of the product suggest an Sn1 or SŅ2 mechanism? Draw the complete mechanism for this reaction, including curved Br OH NaOH CH3 H3C CH3 Br H3C H arrows.Draw a detailed mechanism and show the product for the following reaction. HO H₂SO4
- 10. Draw the complete, detailed mechanism (curved arrows) for the following reaction, and predict the major product. CH3 ▪OH 1. DMSO (COCI)2 2. Et3N HDraw a detailed mechanism for the following reaction, clearly showing all electron movement NH H*, H2O NH46. Determine whether each reaction occurs by an SN2, SN1, E1, and/or E2 reaction. Provide a detailed mechanism with curved arrows and the major product(s). CI NaSH DMF OMs NaOH H20, heat LDA Br DMF NaOH H20, heat OH HBr OH H*, H20 heat
- 11. Determine whether each reaction occurs by an SN2, SN1, E1, and/or E2 reaction. Provide a detailed mechanism with curved arrows and the major product(s). OMs Br Br OH мон OH NaSH DMF NaOH H₂O, heat LDA DMF NaOH H₂O, heat HBr H, H₂O heatPls help, identify the best reagents to complete the following reaction Draw a plausible mechanism for the reaction shown below. Et Ме OH ..Me 1) Excess EtMgBr 2) Hо Et "CI
- !(plz do number 3 , given all possible product , identify major product and give mechanism for each product)6. Determine whether each reaction occurs by an SN2, SN1, EI, and/or E2 reaction. Provide a detailed mechanism with curved arrows and the major product(s). NASH DMF OMS NaOH H20, heat LDA Br DMF NAOH H20, heat OH HBr OH H*, H20 heatDraw a detailed mechanism showing the formation of the product, be sure to draw all intermediate and show the movement of electros by arrows. CH2CH3 CH2CH3 Br,/H>O enantimer Br