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- 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 XPropose an efficient synthesis for each of the following transformations: Br NO2Q1: Identify reagents that can be used to accomplish each of the transformations shown here: a d b OH h
- Fill in the appropriate reagents for the following reaction:1. 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? toShow 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) Он
- Propose a plausible mechanism for the following transformation: HO [H3O+] EtOH 19.55 The first three steps of the mechanism involve the formation of The first step is The second step is The third step is eTextbook and Media Save for Later AttemWhich compound is the major product of the reaction below? HO OH 11419 HO, он TSOH (cat) (A) (В) (D) (C) O Compound B Compound D Compound C Compound A2. Identify the reagents you would use to achieve each of the following transformations: CI 1 2 3 7 4 Br Br 1) 9-BBN 2) H2O2, NaOH 5 ОН CH3 H