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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.The key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold Helminthosporium sativum, involves the following base treatment of a keto tosylate. What kind of reaction is occurring? How would you complete the synthesis?Provide reagents
- Provide reagents/conditions to accomplish the following transformations. Label each reaction type in the steps you provide. OEt MeO OMe1. Provide stepwise synthesis including reagents and intermediates for the following syntheses. OH COOHIndicate the products A and B that are obtained in the following reactions: OH CH3 + HOCH2-CH₂OH + TSOH → A 1° NaH/THF A + →> B 2º C6H5-CH2Cl Briefly comment on each reaction.
- Identify the reagents necessary to accomplish each of the following transformations.The following nucleophilic substitution occurs with rearrangement as shown below. Suggest a detailed mechanism for the transformation using arrows to detail electron flow. Cl ОН NAOH H2OWhat reagents are required to carry out the following synthesis?