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- Show how the product formed as a result of the reaction can be synthesized using the starting materials given below. Any reagent needed can be used and you may need more than one step. c) HO, al OH d) b) ОнFill in the appropriate reagents for the following reaction:Determine a stepwise mechanism for the following reaction that illustrates why two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a weak nucleophile (CH3OH) under Syl reaction conditions, even though it is a 1° alkyl halide. 1-bromohex-2-ene Part 1: Br CH₂OH The first step in the reaction proceeds according to which mechanism? CH₂CH₂CH₂CH=CHCH₂ + CH₂OH CH₂CH₂CH₂CH: Part 2: Br CHCH₂ Draw the missing resonance contributor. OCH3 + CH3CH₂CH₂CH=CHCH₂ CH3CH₂CH₂CH=CH-CH₂ + Br Br OCH 3 H₂CH₂CH₂CH=CH₂ view structure + + Br HBr X
- Fill in the reagents for the following transformations. NO2 NH2 NEN CI CN1. Identify the reagent you would use to achieve the following transformation? Br 2. What reagents and reaction conditions you would use to synthesize following compound? toIdentify the reagents you would use to achieve each of the following transformations.
- Propose an efficient synthesis for each of the following transformations: Br NO2Provide the reagent(s) needed to accomplish the following transformations . Some conversions may require more than one step. If more than one step is required , be sure to enumerate each step.Provide the reagents necessary for the following synthetic transformations. More than one step may be required