Predict the product and draw a stepwise mechanism for the following reaction: Part 1: HBr Br HOH view structure Part 2: HBr H. H20 НОBr Br view structure view structure Но Part 3 out of 4 HO
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- Using any necessary organic and inorganic reagents, show how you can carry out the chemical conversions shwon below. Please answer parts a, b, and c.select the most appropriate reagent(s) to effect the change. 1. Disiamylborane, 2. HO–, H2O, H2O2 H2, Pd K2Cr2O7, H+ NaOCl H2SO4, HgSO4Provide the answer if the compounds will react. 1. Which compound/s will react with Br2 in water under light conditions? (explain each compound; answer may be one or more) 2. Which compund/s will react with I2 in KI under dark conditions? (explain each compound; answers may be one or more)
- Show how m-dibromobenzene can be synthesized from benzene from multiple reactions. Tip: think of diazotation as an important reaction in this process.Complete the reaction by drawing the reactions major organic product and propose a detailed mecanism for it's formationShow the stepwise mechanism for the entire reaction below, including all arrows and intermediates. Your EAS should show at least one resonance form for the sigma complex.
- Propose curved arrow mechanisms for transformations below.d. Reaction with CH3MgI (excess), ether; then H+/H2O e. Reaction with LiAlH4, ether; then H+/H2O f. Reaction with DIBAL (diisobutylaluminum hydride), toluene, low temperature; then H+/H2OPlease provide the answers in each situation. 1. Which compound/s will react with Br2 in water under light conditions? (answer may be one or more) 2. Which compund/s will react with I2 in KI under dark conditions? (answers may be one or more)
- Propose a mechanism for the reaction in Question2.1.3.(a) Propose a plausible mechanism for the reaction given below: (b) Show a plausible step by step synthesis scheme for each of the following transformations:Interestingly, reduction of the complex shown above mostly gives thealcohol enantiomer shown below after workup. a. Draw the other minor diastereomeric alcohol product. b. Briefly explain the diastereoselectivity of the reduction – why is oneenantiomer heavily favored? Draw a structure or structures to support youranswer.