3. Provide a mechanism using arrow pushing for the following enzymatic reduction. Hint - the highlighted hydrogen atoms in the reagents end up in specific sites in the product. HO enzyme H. CH3 CH3 H. `NH2 CH3 CH3 H.
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- Can someone please explain to me how to find which reagents are appropriate for the first image along with the end product and for the second image, how would I go about drawing the mechanism?Show the SN2 mechanism in the reaction between (S) 2-bromobutane and iodide ion. Label the product and draw a enery diagram for this reaction.show the missing reagents and intermediates in the reaction sequence below
- Propose a detailed mechanism for the reaction below (in the attached picture), showing the structure of thestable intermediate and using curved arrows to indicate electron flow in each stepGive the major organic product(s) for each step of the following reactions (d,e,f)The (+) - aureol is a natural product that has shown selective activity against certain colon and lung cancer cell lines. It is postulated that a key step in the biosynthesis of this substance is the conversion of carbocation A into B. Propose a possible mechanism for this transformation (MUST show the corresponding arrows).
- 1. Discuss the role of the Aldol condensation reaction in the synthesis below. What specific reaction was used in the synthesis? What is the importance of the aldol reaction in the entire synthetic approach? 2. Show the detailed reaction mechanism involved in their corresponding specific parts in this syntheses.Provide a detailed mechanism for the following (Hint:halohydrin reaction). Use arrows to show electron flow and show intermediates.1. what is the Nature of the leaving group (LG)? 2. what is the relative size of activation energy (Ea) for each reaction? 3. what is the Hammond's postulate? 4. what are the Relative thermodynamic stability of the reactive intermediates? 5. what is Influence of the solvent (if given) on the reactions and intermediates?