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- Show all the arrow mechanism including the PROPER reagents.Box final answer please.[Review Topics] [References] Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. %3D H3C CH3 HO-CH3 • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na*, I', in your answer. • In cases where there is more than one answer, just draw one. C P. opy Bste C. Previous Next Email Instructor Save and Exit Cengage Learning | Cengage Technical Support 5:50 PM arch 82°F 3/28/2022
- 1. Fill in the necessary starting material, reactants or product for the reactions shown below. A. B. C. I. NaNH,, NH, 2. CH₂CH₂CH₂CH₂Cl 1. NaNH,, NH, 2. CH₂CH₂CI 2. Show the complete mechanism for A. and B. from above. Use the back if necessary.Complete the following reactions with the missing reagent(s) or major product(s).. NaBH, HOBe sure to answer all parts. Draw the products formed through the following reaction. CH3 CH₂ CH₂OH [0] draw structure ... [0] draw structure ...
- Click the "draw structure" button to launch the drawing utility. What alkene is the major product formed from the following alkyl halide in an E1 reaction? CI The major product is: draw structure ...Consider the synthetic sequence shown. Identify the reagents for all three steps. Draw the structures of organic compounds A and B. Omit byproducts.4. Draw the complete arrow pushing mechanism for the following reactions and provide the final product structure. a. b. OH HN H2SO4