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Part IV - Multistep Synthesis [14 marks] A. Propose a synthesis of compound A starting from...
Chem 231, Assignment 5 page 6 of 5 Part IV - Multistep Synthesis [14 marks] A. Propose a synthesis of compound A starting from dimethyl malonate. When choosing your synthetic steps, you can use any hydrocarbon with three or fewer carbon atoms, any solvents or inorganic reagents, and any organic reagents that do not contribute carbon atoms to the carbon skeleton in the product. Clearly show the required reagents and the product of each step. You do not need to...
A. Propose a synthesis of compound A starting from dimethyl malonate. When choosing your synthetic steps, you can use any hydrocarbon with three or fewer carbon atoms, any solvents or inorganic reagents, and any organic reagents that do not contribute carbon atoms to the carbon skeleton in the product. Clearly show the required reagents and the product of each step. You do not need to show mechanistic (curved) arrows. [6 marks) سوني Dimethyl malonate А
Part IV - Multistep Synthesis cont'd Propose a synthesis of compound B from (R)-2-chlorobutane. When choosing your synthetic steps, you can use any hydrocarbon with three or fewer carbon atoms, any solvents or inorganic reagents, and any organic reagents that do not contribute carbon atoms to the carbon skeleton in the product. Clearly show the required reagents and the product of each step. You do not need to show mechanistic (curved) arrows. CI (R)-2-chlorobutane B
Propose a synthesis of compound B from (R)-2-chlorobutane. When choosing your synthetic steps, you can use any hydrocarbon with three or fewer carbon atoms, any solvents or inorganic reagents, and any organic reagents that do not contribute carbon atoms to the carbon skeleton in the product. Clearly show the required reagents and the product of each step. You do not need to show mechanistic (curved) arrows. (R)-2-chlorobutane B
Help with question in image. thankyou. Propose a synthesis of compound B from (R)-2-chlorobutane. When choosing your synthetic steps, you can use any hydrocarbon with three or fewer carbon atoms, any solvents or inorganic reagents, and any organic reagents that do not contribute carbon atoms to the carbon skeleton in the product. Clearly show the required reagents and the product of each step. You do not need to show mechanistic (curved) arrows. CI (R)-2-chlorobutane B
14) Propose a multistep synthesis of the following compound. All carbon atoms in the product must come cyclohexene and from alkanes, alkenes, alkynes, and alkyl halides that contain 3 or fewer carbon atoms. You can use other reagents as necessary. You do not have to draw any curved- arrow mechanisms. While you do not have the products of each synthetic step or explain your synthetic logic, you are strongly encouraged to in order to be eligible for more partial credit....
(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....
4. Synthesis. You may use benzene (that is the starting material for a), any organic reagents that contribute four or fewer carbon atoms to the final product, and any inorganic reagents OH OH HN NH 4. Synthesis. You may use benzene (that is the starting material for a), any organic reagents that contribute four or fewer carbon atoms to the final product, and any inorganic reagents OH OH HN NH
Provide a multistep synthesis for the desired product using the indicated starting materials. You may use any additional organic or inorganic reagents. Do not draw any curved-arrow mechanisms. The best answ will require nine or fewer steps. OH 었 OET NH2 Starting Materials NH3 OH Desired Product
Problem IV. Synthesis (24 points). These transformations will require multiple steps. Provide the reagents for each step and draw out your proposed synthetic intermediates. Please do not draw curved arrows; this prob- lem is not asking for mechanisms. You do not need to provide solvents for the reactions. (1) (12 points) Provide a synthetic route-i.e., a sequence of reactions-to produce compound SS from compound RR using any other starting materials and reagents you wish. RR (2) (12 points) Provide a...