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Synthesize each of the following molecules starting with the indicated organic molecule. Each will require more...
Q2. Synthesize the following product from the given starting compounds. This will require more than one step. You may use any organic or inorganic reagent to carry out this synthesis. (8 pts each) Do (you can also use any one C reagent) ОН (you can also use any two carbon reagent)
02. Synthesize the following product from the given starting compounds. This will require more than one step. You may use any organic or inorganic reagent to carry out this synthesis. (8 pts each) (you can also use any one C reagent)
4-Suggest a synthesis of the target molecule from the indicated starting material. More than one step will be required. For each step of your reaction sequence, show reagents used and product(s) formed. No curved arrows are required.(6 Marks)
4-Suggest a synthesis of the target molecule from the indicated starting material. More than one step will be required. For each step of your reaction sequence, show reagents used and product(s) formed. No curved arrows are required. of N=0 O=0
Design a multi-step synthesis for each of the following target molecules from the indicated starting material. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Draw the structures of the diene and the dienophile that reacted to form the Diels-Alder product shown. Provide the missing reagents in this multistep synthesis.
Provide a reasonable multistep synthesis of the following molecule from the indicated starting material, using any reagents necessary. (Please include the product and reagents of each individual step in your synthesis. DER
Propose a synthesis of the following molecule starting with the indicated starting molecules as the only allowed carbon sources and any needed inorganic reagents. Br B(OH)2 + ethyne ethyl iodide
Devise a multi-step synthesis of the target molecule from the given starting material. Show all necessary reagents and conditions for each step and the product of each step. ОН
Synthesize the target molecule (the one at the top) from each of the two starting materials (each starting material is a separate synthesis). Any additional sources of structural carbons can only have 1 C atom at a time. но. он ОН NH о
H D) Suggest a method to efficiently synthesize each of the following molecules from an alkene using the reactions. we have learned so far. Give the starting alkene and all reagents necessary. In order for the synthesis to be efficient, the desired product should be the major product formed Br Н,с, На Нс 1 CH3 сH, он На сH CH3 2 Нас" Reicion P ,Br 3 осн, CHy Br Н,с. Нас