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When benzene is treated with methyl chloride and Aluminum chloride under conditions that favor trialkylation, one major product is obtained. Draw the product and provide a name for the product.
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- A synthetic organic molecule, G, which contains both aldehyde and ether functional groups, is subjected to a series of reactions in a multi-step synthesis pathway. In the first step, G undergoes a Wittig reaction, leading to the formation of an alkene, H. Subsequently, H is treated with an ozone (O3) reagent followed by a reducing agent in an ozonolysis reaction, resulting in the formation of two different products, I and J. Considering the functional groups present in G and the nature of the reactions involved, what are the most probable structures or functional groups present in products I and J? A. I contains a carboxylic acid group, and J contains an aldehyde group. B. I contains a ketone group, and J contains an alcohol group. C. I and J both contain aldehyde groups. D. I contains an ester group, and J contains a ketone group. Don't use chat gpt.Synthesize the product from the given material. Give the reagents necessary and draw out any intermediate products along the way.Devise concise syntheses for the following transformations. Clearly show the reagent and product foreach step.
- For each compound, show the products obtained from ozonolysis, followed by treatment with dimethyl sulfide.single reaction sequence: a certain ketone undergoes alkylation to give new ketone, when reacted with a base and then an alkylating agent, 1-bromopropane. What is the structure of the final ketone product?Synthesize each compound from benzene. Use a diazonium salt as one of the synthetic intermediates.
- Please provide the reagents for the following transformations.The compound is treated with the base sodium hydride NaH, an intramolecular SN2 reaction occurs. Please draw both the organic intermediate and the major organic product obtained.Draw reaction mechanisms with all reactants, arrows, intermediates, and products. Your mechanism must account for all the products if more than one product is formed. 4-methycyclohexanol with phosphoric acid H3PO4 to for 1-methycyclohexene, 3- methylcyclohexene and 4-methycyclohexene
- An alkene is treated with OsO4 followed by H2O2. When the resulting diol is treated with HIO4, the only product obtained is an unsubstituted cyclic ketone with molecular formula C6H10O. What is the structure of the alkene?Show how you would synthesize octan-2-one from each compound. You may use any necessary reagents.(a) heptanalThe following synthesis requires more than one step. Specify the reagents you would use to carry it out.