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- Please predict the outcome of each reaction below: Type you answer as a letter: A, B, or F. Problem 1: https://doi.org/10.1021/ol101705j & Answer to Problem 1: Hint 1. Assume the reaction can ONLY occur at the MOST ELECTRON RICH double bond. Hint 2. Assume the reaction can ONLY occur from the least sterically hindered side of the molecule. Draw or build a 3- dimentional conformation to support your answer. ? H H H A 1 equivalent m-CPBA H H B H сDraw the major product of this reaction? 10 لله 024, 17:21 Br₂ one equivalent ?I have attached a picture showing the questions i have. Numbers 5B and 5C are where i am confused.
- Part G Interactive 3D display mode H3C CH3 BrWhat would be the AXE notation for Pbl2? O AXE2 O AX2 O AX2E3 O AX2E2 O AX,EChoose the correct IUPAC name for the following compound (Do mention cis or trans, E or Z, or R or S stereochemistry where necessary) O a. (1R,2R,4S)-2-fluoro-4-methylcyclopentanol b. cis-trans-2-Fluro-5-methylpentanol C. cis-trans-2-Fluro-5-methylcyclopentanol O d. (1R,2S,4R)-2-fluoro-4-methylcyclopentanol R,4S)-2-fluoro-3-methylcyc entanol e. NEXT PAGE