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- #16c. Provide the missing reactants, reagents, or products for the following reaction sequences below.5) Describe what reaction or sequence of reactions could bring about the following transformation. H سيق ? H ・エ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.
- Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated , -unsaturated isomers. Propose a mechanism for this isomerization.4) Give an example of an enol which would tautomerize into a) an aldehyde and b) a ketone.11.7_7 Which of the following conversions is essentially irreversible? A) The reaction of an aldehyde with a Grignard reagent. B) The reaction of a ketone with an alcohol. C) The reaction of an aldehyde with a 1° amine. D) The reaction of an alkene with water in the presence of acid catalyst. A
- Provide the necessary reagents to accomplish the desired organic reactions. Please number the steps and note that some reactions will require more than one step.1. Methylene cyclohexane, on treatment with strong acid, isomerises to yield methyl cyclohexene. Propose a mechanism by which the reaction might occur.4. Aldehydes and ketones can be “protected" as acetals and ketals. Complete the following outlined reactions, showing how the protection is accomplished, and what results after deprotection. MgCI 1) 2) HO* deprotection here