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* * * FIVE STAR * * On your own. Please devise synthetic pathways for the...
Ochem transformation pathway help Devise a viable synthetic pathway to achieve the following transformations. You may use any inorganic reagents and any other organic compounds containing two carbon atoms or fewer. You do not need to show any mechanisms. Multiple steps are needed.
Devise a synthetic scheme that converts the organic reactant to the product shown below. You may use any organic and inorganic reagents necessary. Multiple Steps HO OH
(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....
Devise a synthesis of the following compound using the given compounds (you may use each one more than once if needed). You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials.
9. Devise a synthesis of the following compound using the given lactone. You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials.
9. Devise a synthesis of the following compound using the given lactone. You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials.
2) Devise a synthesis of the following compound using only ethanol. You may also use any needed Inorganic or organic reagents but all of the carbons in the target molecule must come from ethanol. Hint: this synthesis will require you to use a Claisen reaction
just need help with the one with the star in the middle 1. The following transformations cannot be performed in one step. Provide a sequence of reactions to convert the 'starting material to the "product. Show all the reagents and synthetic intermediates. You can use any additional carbon sources if needed, but you must use the starting material oiven. Br Oz7 mezo OH
3) Devise a synthesis of the following compound using the given compounds (you may use each one more than once if needed). You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials. Hint: this synthesis will require you to use ozonolysis and a reaction that starts with the letter DI
Show, by writing a series of synthetic steps how you could prepare the following target compound for the designated two starting materials (a cyclic diene and acetylene) and any other necessary organic or inorganic reagents. You must also show all the intermediate structure(s) for your synthesis indicated by the "?" marks. More than one step will be needed. H CH,CH, CH CHH + H-C=C-H ? ?