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HELP PLEASE ANSWER ALL III. Predict the major product(s) or fill in the reagent(s) for the...
organic
III. Predict the major product(s) or fill in the reagent(s) for the following reactions. If there is no reaction write NR. (6 points each, 36 points total) Show the correct stereochemistry when needed!! 16 HO H,Cro (excess) -CHO 17 1)0, (2 equiv.) 2) Mezs (2 equiv.) 18 Ph Ph он om Ph Ph 19 1) mCPBA 2) EtONa, EtOH 20 1) LIAIH (excess) 2) H20*, ,0+ 21 1) NaNH, 2) CH,Br 3) HBr (2 equiv.)
III. Predict the major product(s) or fill in the reagent(s) for the following reactions. If there is no reaction write NR. (6 points each, 36 points total) Show the correct stereochemistry when needed!! 16 H,Cro (excess) -CHO HO 17 1)0, (2 equiv.) 2) Mes (2 equiv.) 18 Ph Ph Ph Ph OH
Please answer ASAP. Will rate if correct. Thank you.
Predict the major product(s) or fill in the reagent(s) for the following reactions. If there is no reaction write NR. (6 points each, 36 points total) Show the correct stereochemistry when needed!! 16 HO H2Cr04 (excess) -CHO 17 1)03 (2 equiv.) 겨 2) Mezs (2 equiv.) 18 Ph Ph LOH om Ph Ph
19 1) mCPBA 2) MeOH,H 20 1) LIATH (excess) 2) H20+, H30+ 21 1) NaNH, 2) CH,CH,Br 3) HBr (2 equiv.) 22.Draw DETAILED arrow.pushing mechanisms for the following transformations: (8 points) H-Br: ër:
Predict the major product in each of the following
transformations. No mechanisms are required for this question.
Predict the major product in each of the following transformations. No mechanisms are required for this question. [3 Marks] 1. CH,CHMgBr (excess) hoy 2. HCl(aq) i 1. PhMgør (1 equiv.) 1. PhMgBr (1 equiv.) 2. HCl(aq) охон 1. CH3MgBr (2 equiv.) 2. HCl(aq) Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by drawing the overall balanced...
Predict the major product in each of the following transformations. No mechanisms are required for this question. [3 Marks] 1. CH3CH2MgBr (excess) 2. HCl(aq) 1. PhMgBr (1 equiv.) 2. HCl(aq) ОН о но 1. CH3MgBr (2 equiv.) 2. HCl(aq) н Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by drawing the overall balanced equation. No mechanisms are required for this question. You do not need to show formation of the Grignard reagent. [2...
2. Predict the major organic product(s) of the
reactions below. Assume 1 equivalent of reagent unless otherwise
stated, it's a solvent, or an oxidizing/reducing agent. Do consider
stereochemistry and regioselectivity.
2. Predict the major organic product(s) of the reactions below. Assume 1 equivalent of reagent unless otherwise stated, it's a solvent, or an oxidizing/reducing agent. Do consider stereochemistry and regioselectivity. (3 points each; 15 points total) A. Me 1. HNO3 2. O3 3. DMS 1. mCPBA, DCM (1 equiv) 2....
11. Predict the major organic product(s) for the following reactions. If there is no reaction write N.R. (6 points each, 72 points total) Show the correct stereochemistry when needed!! -OH HSO heat 1) 0, (2 equiv.) 2) Meys (2 equiv.) HC104 excess CHO NaBH4 (excess) HO CHOH Br ON HỌ, PHÚC
Predict the product(s) and reagent(s) or if there is no reaction
write NR.
OH K2Cr207 (excess) H2SO4, H20 "ОН 1. PhLi, Et20 2. HCI, HO 3. SOCl2, Et3N 4. NaOAC 1. Mg (1 eq), Et20 < Br 2. (1 eq) CHO 3. HCI, H2O MsCI LDA ОН pyridine 1. Nah 2. Br
Predict the product(s) and reagent(s) or if there is no reaction
write NR.
041 for 1. NaBH4, MeOH, 0°C 2. PBr3, THE 3. LiAlD4, THE 4. HCI, H20 1. SOCl2, NEt3, THE CHO 2. 2 eq Li, hexane 3. HCI, H2O OTE hint: multiple steps 1. LIAIH4, THE 2. HCI, H2O 3. PBr3, THE CN OH 1. PCC, DCM 2. Mg, Et O 3. HCI, H2O 1. MSCI, pyr 2. KO'Bu, BuOH