predict the major products of the following reactions with appeopriate stereochemistry mCPBA lal H2O OH (b)...
predict the major products and if it's undergoing oxidation or reduction 23 a. mCPBA) b. Noh H2O H2SO4 C. 79E+OH ) H₂SO4 d. Bar tok e. F 1) O3 2) DMS f. K. Hz Pt ->
9. Predict the major products for the following reactions. Show the stereochemistry of the products) when applicable.. (a) HIB ROOR (1) Hg(OAc), HO (2) NaBH (1) BH, THE (2) 1,0, OH Br. H.O Pt (1) Oso (2) NaHSOHO (1) 03 (2) DMS (1) CHCO,H (2) H0+ Page 2 of 2
11-41 Predict the major products of the following reactions, including stereochemistry where appropriate. 1,41 X) CH,OH + pha Z) a oua - 7) W--butanol Play Br →
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....
1. Predict the major organic products formed in the following reactions. Be certain to indicate stereochemistry in your products if it is important. (12 pts) Pd/C u o H2O H2SO4
complete the following reactions with the proper stereochemistry as need оCHbb H2SO4 (dilute) OH H2O HBr (conc) но H но heat но но H CHs MCPBA OH Jones (CrO3. H,SO4) H2O, acetone 1. MCPBA OH PCC 2. NaCN 3. Hy0 pyridinium chlorochromate CH2CI2, 25 C 1. MCPBA PCC OH pyridinium chlorochromate 2. HBr Cн-Cl, 25 C NaBH OH Hао 1. DMSO, (COCI)2, -60C 1. LIAIH 2. Et N 2. H,0 оCHbb H2SO4 (dilute) OH H2O HBr (conc) но H но...
1. Predict the major organic products of the following reactions. Draw all stereoisomers that are formed. НО, OH 1 eq ,H2SO4 (assume H2O workup of reaction to neutralize product) 1. LDA 2. (assume H,O workup of reaction to neutralize product) 3. Hg(OAC)2 4. NaBH, EtOH 1eq HBr EtOH ambiente 1. Brz. CCL 2. NaOET, ETOH OH
1. Predict the major substitution product(s) for the following reactions. Include stereochemistry if appropriate. You may assume an aqueous workup is performed after each reaction. 1. Nah, DMF ТОН 2. Mel BrMg-Ph KCN 16 { ad ton ot MeOH HD Na Br Me DMSO EtOH Br ~ Br DMSO * Me OH LNH2 M HO Me-S (1 equiv) Me DMF
Predict the major organic products formed in the following reactions. Be certain to indicate stereochemistry in your products if it is important. H2 Pd/C HCI H2O H2SO4 Br2 Draw a stepwise, detailed mechanism for the acid-catalyzed hydration reaction in question 2 above. Use curved arrows to indicate the flow of electrons. (Note: use hydronium ion, H307, in your mechanism to indicate “acidic water”).
Predict the major organic products formed in the following reactions. Be certain to indicate stereochemistry in products if it is important. H2O H2SO4 Br2 3. Draw a stepwise, detailed mechanism for the acid-catalyzed hydration reaction in question 2 above. Use curved arrows to indicate the flow of electrons. (Note: use hydronium ion, H:07, in your mechanism to indicate "acidic water"). (6 pts)