Provide the synthesis, including the substrate, major intermediate(s), reagent(s), and product for the transformation below: If stereoisomers are generated, add them in the order as the products they generate.
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- Represent the products that would be obtained in each of the reactions below (leaving the stereochemistry clearlyrepresented, in the case of products from stereospecific reactions) and classify them in relation to what occurswith the substrate, indicating whether they are: mild oxidation, oxidative cleavage or reduction.Give the substitution and elimination products for the following reactions, showing the configuration of each product. It develops all the steps of the reaction mechanisms.Predict the product of the following reaction, and provide the reaction mechanism
- Provide the major product(s) produced from each of the following reactions.Give the major products for the following reactionAn elimination step is involved in the synthesis of aromatic amino acids. We can also envision this occurring in a laboratory setting with a strong base. Provide a 1 step mechanism for this decarboxylation reaction. Note: under strongly basic conditions, hydroxide is a reasonable leavinggroup.
- (a) A student was given a task to synthesize the products as shown below. Analyze the reaction schemes below and state whether the reaction conditions supplied in each reaction scheme will result in the products shown as MAJOR PRODUCTS. If wrong products are shown, draw the correct products and provide mechanistic details (curly arrows) of how the right (major) products were formed. E CI t-BuOK t-BuOHIf possible please answer all questions. Provide the major product(s) produced from each of the following reactions.A ketone undergoes acid-catalyzed bromination, acid-catalyzed chlorination, racemization, (see page 408)and acid-catalyzed deuterium exchange at the a-carbon. All of these reactions have similar rate constants.What does this tell you about the mechanisms of these reactions?