5. Synthesize the following product from the starting material given. Provide reagents and intermediate products for each step. a) OH Br b) OH HO
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- Provide all the reagents and show all structures of the product formed in each step, not just a list of reagents. b) Benzene c) Toluene OHC Ĵ Ĉ COOHProvide 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.Show how to synthesize the following product as the major product starting with 2,2- dimethylpropane as the starting material. You may use additional reagents and any number of steps. Be sure to list each step with all reactants/reagents/conditions required. (Do not use hydrogenation reactions) from
- 4) Synthesize the following molecule using the indicated starting material, showing all reagents used in each step. H. from CN H HO EtO1. Complete the following syntheses starting from a) & b) acetoacetic ester and c) malonic ester. Provide the appropriate reagents and alkyl halides in the provided boxes. a) b) 1 2 3 1 2 3 1 2 ая 3 1 c) LOH 2 3Provide the necessary reagents to accomplish the desired organic reactions. Please number the steps and note that some reactions will require more than one step. Me Meo. Meo. CF MeO
- 1. Provide stepwise synthesis including reagents and intermediates for the following syntheses. OH COOHShow how to synthesize the following product as the major product starting with 2,2-dimethylpropane as the starting material. You may use additional reagents and any number of steps. Be sure to list each step with all reactants/reagents/conditions required. (Do not use hydrogenation reactions). Write the process.b) The Wolf-Kishner reduction is a reaction used in Organic Chemistry to convert carbonyl functionalities into methylene group. The reaction was used to convert an aldehyde or ketone to an alkane using hydrazine, base and thermal conditions. The mechanism begins with the attack of hydrazine of the aldehyde or ketone. Stage 1: The reaction of aldehyde/ketone with hydrazine to produce hydrazine Stage 2: Reaction with the base and heat to convert hydrozone to alkane Write the mechanism of the reaction.