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- How does doubling [B:] affect the rate of an E1 reaction?Please provide a mechanism with curved arrows by replacing MgBr with 3-methoxyphenylmagnesium bromide and the final product should be 3-methoxybenzoic acidExplain why the following cyclohexanol A derivative undergoes E2 more readily than cyclohexanol B. State three reasons.
- From the table of available reagents select the one(s) you would use to convert l-phenylethanol to m-bromobenzoic acid Use the minimum number of steps; in no case are more than two steps necessary. List reagents by letter in the order that they are used; example: fa. Reagents available a. BH3, THF; then H2O2, OH d. KMNO4, H2 O g. PhMgBr; then H30+ b. Br, FeBr3 e. LIAIH4; then H30* h. POC13, pyridine c. CH;MgBr; then H30 f. PCC, CH2 Cl2 Submit Answver Try Another Version 10 item attempts remainingHow would you synthesize the following compounds from cyclohexanone using reagents from the table? Use letters from the table to list reagents in the order used (first at the left). Reagents a 1. CH3MgBr/dry ether 2 H3O+ e 1. OsO4 i 1. BH3/THF 2. NaHSO3/H2O 2. H₂O₂ / NaOH b 1. C6H5MgBr / dry ether f 1. NaBH4 j Mg / dry ether 2 H3O+ 2. H3O+ с PBr3 g HOCH2CH2OH/HCI k H2/Pd d m-chloroperbenzoic h H3O+ / heat I CrO3 / H3O+ acid m cyclohexanone a) cyclohexylbenzene b) 2-phenylcyclohexanone Submit Answer Try Another Version 3 item attempts remainingHow would you synthesize the following compounds from cyclohexanone using reagents from the table? Use letters from the table to list reagents in the order used (first at the left). Reagents a 1. CH3MgBr / dry ether 2 H3O+ e 1. OsO4 i 1. BH3/THF 2. NaHSO3/H₂O 2. H₂O₂ / NaOH b 1. C6H5 MgBr / dry ether f 1. NaBH4 j Mg / dry ether 2 H3O+ 2. H3O+ C PBг3 g HOCH2CH2OH/HCI k H2/Pd d m-chloroperbenzoic h H3O+ / heat 1 CrO3 / H3O+ acid a) 2-phenylcyclohexanone b) cyclohexylbenzene m cyclohexanone