3) Propose a synthesis scheme for the following molecule from benzene using any reaction conditions. 4)...
Design a scheme and draw the mechanism for the synthesis of the following compound from benzene and an alkyl halide. Application Questions 1. Design a scheme and draw the mechanism for the synthesis of the following compound from benzene and an alkyl halide. For the compound in application question one, design a scheme and draw the mechanism for the synthesis from benzene and an alcohol. 2. Explain why you cannot directly form the following compound from a Friedel-Crafts alkylation of...
(4pts) Propose a synthetic scheme from benzene and any other organic or inorganic reagents for the following compounds. a. COOH ci SOH NH2
4. Propose a synthesis of the molecule below starting with benzene. You should consider using an arenediazonium salt. (2 points) CH2CH3
4. Propose a synthesis of the molecule below starting with benzene. You should consider using an arenediazonium salt. (2 points) CH2CH3
9. Propose an efficient synthesis of each molecule below starting from benzene and any other reagents needed (organic or inorganic) A. CI B. CI NO2 Br
4. Propose an efficient synthesis of the molecule below starting with benzene. You can use any other reagents you want. NOTE: Some reactions produce ortho- and para-products. It is allowable to just take ONE of the products and use it in the next synthesis or claim it as the final product (we assume that ortho- and para-products can be separated). (3 points) CH2CH2CH Br
12.) Propose a reaction scheme/conditions (all reagents for each step) to synthesize the following product from benzene. (8 points) SO3H
2. Propose an efficient synthesis (less than 5 steps) of the following molecule from benzene. You may use any additional material and show all intermediates. Br HO
Propose a step-by-step synthesis to prepare the following compound from benzene, using any reagents needed. =O ZI
Propose an efficient and elegant synthesis of the molecule using only a benzene as your starting material. You may use any alkyl halide or alcohol as your other sources of carbon (excluding HCOCl), and any other reagent you deem necessary. OH Cl