. Design and write all the steps in sequence for the following transformation. Show all the reagents and product for each step, leading to the final product shown here. No mechanism is required. steps F CN steps
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- The transformation below takes place by two distinct reactions. Intermediate A is formed in the first reaction and then this goes on to the product in the second reaction. Provide a complete curved-arrow mechanism for all steps of both reactions.Draw the major substitution and elimination products for the reaction shown below. You must show the correct stereochemistry where applicable.Please show detailed mechanism how this transformation is achieved
- Show how to synthesize the following product as the major product using any reactants/reagents and number of steps. Be sure to list each step with all reactants/reagents/conditions required. (Do not use hydrogenation reactions)Supply the missing reagents and intermediates (A—C) in the following synthesis. please explain steps2. Draw the product for following reacttons. Propose mechanism for each of reactions. a) DCI
- Provide the mechanism for each step of the given reaction, showing the major product as well.For each of the following reactions draw the structure of the major organic product in the box provided.Each numbered set of reagents above or below the arrow represents a complete separate reaction.For multi-step reactions give only the structure of the final product.Complete the following reactions by identifying the majority product(s) or the reaction conditions that are missing. No mechanism is needed