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- 11:47 PM Fri Mar 3 ← Select to Draw cat. H2SO4 SO3 (1 equiv) Select to Draw ●●● Problem 49 of 21 Please select a drawing or reagent from the question area 18% SubmitPara çi (G) + Noa E H NOa Because of electr Substituton Para and ortho the favored pOsitio Stable VI. Draw the two possible intermediates for the attack of the nitronium ion on naphthalene including the important resonance structures. Which position is favored? Why? 28 Ahayden 12Current Attempt in Progress What would be the major product obtained when trans-1-bromo-3-methylcyclopentane is allowed to react with NaSH at 25°C? SH H3C SH H3C WH H H₂C 01 I Oll OIV H H₂C SH II O Equal amounts of I and II O III Save for Later Hill III iller IV H Br Attempts: 0 of 2 used Submit Answer
- Which of the following reactions will not yield a carboxylic acid as a product? он (B) owool CrO3/H,0 (1) Oz/CH;Ch, -78°C (1) Mg, ether, A (A) Br (C) (2) H20 (2) CO2 (3) H* (dil /H¿O он H* /H2O A (D) Reaction D Reaction A Reaction CI Draw the organic product formed when cyclopentene reacts with iodobenzene in the presence of triethylamine and a Pd(0) catalyst. + (CH3CH₂)3N Pd(0) catalyst Select Draw C Rings H | More EraseEnolates react with a B-unsaturated ketones to afford the 1,4-addition product. What is the expected product A for the following reaction sequence? NaOEt EtO OEt ELOH *last picture 3/5 answer choices, not enough space
- 36. Which of A - E is the most likely product of the following reaction? [A] Br Mg ether OH [D] 1. 2. 30 [B] OH ? OH (E) [C] LOH- 32 What is the organic product? (Hint: A ring structure undergoes loss of H₂O in the last step to form the observed product) H A B go H NaOH H₂O C D HO ?Br LiCu(CH3)2 6 (1) LiAlH4 2 3 Ahol follow (2) H₂O 0 Aci HBr (xs) H (2) H₂O+ -Li