Determine the most likely mechanism and predict the major product for the reaction below. (choose 1 mechanism and all major product(s)) CI NO2 CI NaOH
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- Predict the most likely mechanism for the reaction shown below. CI CH₂ CH3 H₂O ABe sure to answer all parts. Draw all products, including stereoisomers, in the following reaction. NaOH CI Part 1: Identify which mechanism(s) the reaction will undergo. Sy1 Sy2 O El 2 E2 Part 2: The number of S 2 product(s): 1 The number of E2 product(s): 2 Part 3 out of 3 The Sy2 product: draw structure . The E2 products: draw structure . draw structure . (major) (minor) Need help with part 3D Me H 1) BH3, THF 2) H₂O₂, NaOH, H₂O Give the mechanism and product(s) for Step 1. Give the product(s) for Step 2. No mechanism is necessary for Step 2.
- The accepted mechanism for a rearrangement reaction is shown below. "Q Ph (1) (ii) Ph Ph HO™ fast Ph Ph HO O™ slow Ph aufae .Ar² LOH HO™ fast Draw a curly arrow mechanism for this transformation. Sketch an energy profile for this reaction, showing approximate relative energies for the reactants, intermediates, transition states, and products. HQ Ph (iii) When DO™ was used as the reagent, the rate of product formation was same as for HO™. Explain why this result shows that the third step is fast and cannot be rate-determining. Ph (iv) Write the predicted rate equation for this mechanism, and show how it was derived. (v) The starting diketone may have two different aryl groups, as shown below. Propose a ¹³℃ labelling experiment that would allow you to distinguish which of the two aryl groups had migrated in this situation. OH AR²0- Ar¹ C CVII. (i) Show the major product for the following reaction AND (ii) propose a reasonable mechanism for the reaction. O CH3 CH3 Mechanism: excess HI major productProvide the mechanism and products for the acid-catalyzed epoxide opening reactions below, including appropriate stereochemistry.