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- 2) Fill the boxes with the expected products for the following reactions: (6 pts) NO2 NH2 MeOH RT - H₂O H2 Pd-C HCI EtOH(14) Mechanism :0 Ö NaOH 1 -0²³Which is an appropriate name for the following compound? (2R,4S)-1,2-epoxy-4-ethoxypentane 2-ероху-4-ethoxypentane O(2R,4R)-1,2-epoxy-4-ethoxypentane (2R,4R)-1,2-ероху-4-еthoxypentane (25,4R)-4,5-epoxy-2-methoxypentane (2R,4S)-1,2-epoxy-4-methyl-5-oxoheptane
- List in order of increasing nucleophilicityWhat is/are the major organic product(s) for the reaction shown below? LOH (2) Bri Brzy ? Febr3 (700)) Br CH Oft Br от ва сохо x DO I CHO II Br 7 OH cmd option OY V (8 CAD Only V (B) only I and II CD) Only II and IV (E) only I and IV III OH Br IV OH CO only 1, II, and IV O-8° 20 What is the major product of the reaction shown below? H₂ Pt, heat Question 24 of 31 MA MacBook Pro AA A) butane B) 1-butene C) 1-butyne D) 2-butyne E) No reaction occurs. DII DD (1 (1)
- 8.57 Predict the major product(s) for each of the following reactions: H2 (PPh3)3RhCI ? (a) (b) ? (c) (d) 1) BH3⚫ THF 2) H2O2, NaOH 1) RCO3H 2) H3O+ ? H3O+ ?2:50 27 eBook ✔ Print n References Predict the major product(s) in the reactions below. 1) NaNH, 1) NaNH, 2) CH₂Br 2) 1-iodohexane HC=CH Multiple Choice O O 1-nonyne 2-nonyne cis-2-nonene trans-2-nonene 4G 79%Para 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 12
- Current 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 AnswerI 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