5. Synthesize the following product from the starting material given. Provide reagents and intermediate products for each step. a) B OH B Br HO OH
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- 3) Draw the structures of the major organic product(s) for the following reactions. HI in CH₂Cl₂ 3 excess Cl₂ in H₂O H₂SO4 in H₂O (Two products) Br-Cl in THF 1) BH3 2) alkaline H₂O₂ OSO4 + HOOHBicyclo-2,5-heptadiene can be prepared in two steps from cyclopentadiene and vinyl chloride. Provide a mechanism for each step.The pictured reaction shows an alkyl bromide being converted into an alkene. Choose all reagents that would produce the pictured alkene as the major product. A) NaOH/H2O B) H2O C) tBuOK/tBuOH D) EtONa/EtOH
- INDICATED reaction by filling in any Starting materials, reagents or products as needed.Fill in the missing structure(s) for the reaction pathways shown below. Provide allstarting material(s), reagent(s), or product(s). If more than one product can be formed,draw all major products. If more than one starting material or reagent is possible, writeall starting materials and reagents.To synthesize the following substances using any alkene as a starting material. Name the starting material.
- Provide a step-by-step mechanism to account for the product of each of the following reactions. Show the structure of each of the intermediates and use curved arrows to indicate electron flow in each of these steps.please don't provede handwritten solution..5. Propose the synthesis of the following compounds (any two) from benzene using diazonium replacement reaction. coH HOH a) b) c) CH3 CI