Propose a synthesis of the following molecule starting with the indicated starting molecules as the only allowed carbon sources and any needed inorganic reagents.
Propose a synthesis of the following molecule starting with the indicated starting molecules as the only...
Propose a synthesis of the following molecule starting with the indicated starting moleucles as the only allowed carbon sources and any needed inorganic reagents. Cl anisole ← H3CO Cl
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
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
Propose syntheses of the following molecules, starting from benzene, toluene or phenol, any inorganic reagents and any organic reagent of TWO carbons or less: 4. Propose syntheses of the following molecules, starting from benzene, toluene or phenol, any inorganic reagents and any organi c reagent of TWO carbons or le a) NO2 b) CO2H c) OH d) e) NO2 NO2 Br CI CI CO2H Br
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformation in good yield. Use the given compounds as the only organic source of carbon atoms. You may use any common organic solvents as well as any needed inorganic reagents (14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI....
Starting only from organic reagents of 4 carbons or fewer, propose an efficient synthesis for the molecule below. You may use any necessary solvents and inorganic reagents, and can assume that all products can be isolated as needed. If only one product is to be taken on to a new step, indicate which one.
1. Propose a synthesis for either of the following molecules using the indicated starting materials. You don't have to use all of them, but all your carbon atoms must come from them alone. (Hint: A five membered lactone will spontaneously form from the correct hydroxy acid.) If you provide syntheses for both a 10 pt bonus will be awarded. OH со, КCN Br н Н NO, Br NH2 2. Propose a mechanism to account for the following reaction. Used the...
Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. If equal mixtures are anticipated (i.e. ortho / para products) then indicate where separations are needed. NO MECHANISMS! [6 points 2. Give a...
9) (marks = 3) Provide a reasonable multistep synthesis of the following molecule from the indicated starting material, using any reagents necessary. Please include both a retrosynthesis and a forward synthesis (that includes the product and reagents of each individual step in your synthesis). Meo. = Me Me as a racemic mixture These reagents are your only sources of carbon and both are to be used at different steps of your synthesis
4.) Propose a synthesis of the following molecule from hydrocarbons of five carbons or fewer and any inorganic reagents you need. 4.) Propose a synthesis of the following molecule from hydrocarbons of five carbons or fewer and any inorganic reagents you need. Z - I