Part 2 of 2 Provide the structure of the ozonolysis product of the most stable alkene from Part 1 shown below. 1.0, 2. Zn, H₂O Click and drag to start drawing a structure.
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- b. 1. Propose a detailed stepwise mechanism, using curved arrow notation, for the following. H* LiOH OH a. H H₂O, heat 1. LIAIH4 (xs) 2. H₂O e NH₂ + H H-NⓇ HProvide the structure of the ozonolysis product of the most stable alkene from Part 1 shown below.FoE M M FoE * all 61% • .. 10:26 A What is the major Organic product of the following Wolff-Kishner (reduction) reaction? C-CH3 H-NNH, KOH ?? OH NNH, C-CH CH.CH, C-CH NHNH, NHNH, (ci (d) b) (a)
- 1. (10 points) Complete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible answer. Do not neglect stereochemistry. NaCN DIBAL Br A "OCH3 (sodium cyanide)Give clear handwritten mechanism of the reaction with curved arrows!(Explain all point of question with proper type the answer) .
- 15.4 (jkl) Predict the major product or reagent that completes the transformation3. (15 points) Complete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible answer. H20 a) H20 LIAIH4 b) H3O*BONUS 1: Multistep Synthesis: Provide the final product(s), when anisole is treated with the followin reagents. Consider the predominant product(s) in each synthetic step. 1. 2. Br₂, FeBr3 - consider mono-bromination ONLY as the predominant outcome here HNO3, H₂SO4
- Provide the product or reagent that completes the reactionsH3C a. (6 points) Provide the curved-arrow mechanism for the first halogenation reaction; reaction intermediates are provided. H H e.. : OH Na H₂C H :|-| H3C4.1- The following 3 transformations involve Diels-Alder reactions. Draw the product and stereochemistry with a mechanism for all three (continued on next page). OMe heat