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CI OR C D Glve the proper series of reactions, using reagents from the table below,...
W ОН CI E F Give the proper series of reactions, using reagents from the table...
W ОН CI E F Give the proper series of reactions, using reagents from the table below, that will carry out the overall transformations shown. (Assume aqueous workup where needed.) 1. Brz/ uv light 2. SOCI2 / THE 3. Mg/Et20 4. Meli/hexane 5. CH3CH2 MgCl 6. PhMgBr 7. NaBH4 8. LIAIHA 9. BH3 / ox 10. POC13/pyridine / THE 11. CrO3/THE 12. PCC/ CH2Cl2 13. Ht / H20 14. ELOH/H 15. t-butoxide 16. OH/H20 17. NH3 18, CO2 19. acetic...
A1 A 42 NH, OEt B1 OH B B2 ОН Me Me ОН C1 Ph C2...
A1 A 42 NH, OEt B1 OH B B2 ОН Me Me ОН C1 Ph C2 C OH Give the proper reagent for each of these two-step reaction sequences. Pick the reagent from the table below. (Assume aqueous workup when needed.) 1. Br2 / uv light 2. SOCI2 / THE 3. Mg/Et20 4. Meli/hexane 5. CH3CH2MgCI 6. PhMgBr 7. NaBH4 8. LIAIH4 9. BH3 / 0x 10. POCI3/pyridine / THE 11. CrO3 / THE 12. PCC / CH2Cl2 13. H...
OH OH B no Give the proper reagent (from the table below) that will carry out...
OH OH B no Give the proper reagent (from the table below) that will carry out the transformation shown for each step. (Assume aqueous workup where needed.) 1. Cl2 / uv light 2. Br2 / uv light 3. Mg/Et20 4. Li metal/hexane 5. propanal 6. PBr3/THE 7. CrO3/THF 8. PCC / CH2Cl2 9. CH3CH2CH2MgCl 10. NaBH4 11. acetone 12. OH 13. H7H20 14. BH3 / ox 15. t.butoxide 16. PhMgBr Enter a number, 1 through 16, for each answer. Step...
MgCl Ph Ph Give the proper reagent (from the table below) that will carry out the...
MgCl Ph Ph Give the proper reagent (from the table below) that will carry out the transformation shown in three steps. (Assume aqueous workup where needed.) 1. Cl2 / uv light 2. Br2 / uv light 3. Mg / Et20 4. Li metal/ hexane 5. H2C-O 9. CH3CH2MgCI 10. LiAIH4 13. Ht /H20 14. BH3/ox 15. H2/Ra Ni 16. PhMgBr 6. PBr3/THF 7. CrO3/THF 8. PCC/ CH2CI2 11. TMS-cl/R3Nİ 12. SOCb Enter a number, 1 through 16, for each answer...
Multi-step synthesis ci R R NH, OEt А OH B 1. Br2 / uv light 2....
Multi-step synthesis ci R R NH, OEt А OH B 1. Br2 / uv light 2. SOCI2 / THE 3. Mg/Et20 4. Meu/hexane S. CH3CH2MgCl 6. Ph MgBe 7. NaBHA 8. LAHA 9. BH3 /OX 10. POCl/pyridine/ THF 11.03/THE 12. PCC / CH2 13.H/H20 14. ELOH/H 15. t-butaxide 16. OH/H20 17. NHS 18.CO2 19. acetic anhydride 20.HNMez/THE In each box, type out the list of reagents in proper order that will carry out the synthesis of the final product (This...
Propose an efficient synthesis for the transformation below. Enter the appropriate number of letter from the...
Propose an efficient synthesis for the transformation below. Enter the appropriate number of letter from the reagent list handout Step 1 Step 2 Step 3 OH Alkyl Halides (X = CI, Br or 1) and Acyl chlorides: Assume Allig 15 present, if needed CIP CU CH3X X CI E A B EE Ketones. Aldehydes and Epoxides: Assume "then H20" is included if a protonation step is needed F A A K 0 MN Р Grignard, Wittig and Organocuprate Reagents: Assume...
Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number...
Propose an efficient synthesis for the transformation below,
using two sequential reductive aminations. Enter
the appropriate number or letter from the reagent list handout.
Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number or letter from the reagent list handout. Step 1 + NaBH3CN, H+, Step 2 - NaBH3CN, H+ Reagent List (Updated 4/30/2020) Enter # or letter in the appropriate boxes. Note: Exam responses are case insensitive Alkyl Halides (X = Cl,...
W ОН CI E F Give the proper series of reactions, using reagents from the table below, that will carry out the overall transformations shown. (Assume aqueous workup where needed.) 1. Brz/ uv light 2. SOCI2 / THE 3. Mg/Et20 4. Meli/hexane 5. CH3CH2 MgCl 6. PhMgBr 7. NaBH4 8. LIAIHA 9. BH3 / ox 10. POC13/pyridine / THE 11. CrO3/THE 12. PCC/ CH2Cl2 13. Ht / H20 14. ELOH/H 15. t-butoxide 16. OH/H20 17. NH3 18, CO2 19. acetic...
A1 A 42 NH, OEt B1 OH B B2 ОН Me Me ОН C1 Ph C2 C OH Give the proper reagent for each of these two-step reaction sequences. Pick the reagent from the table below. (Assume aqueous workup when needed.) 1. Br2 / uv light 2. SOCI2 / THE 3. Mg/Et20 4. Meli/hexane 5. CH3CH2MgCI 6. PhMgBr 7. NaBH4 8. LIAIH4 9. BH3 / 0x 10. POCI3/pyridine / THE 11. CrO3 / THE 12. PCC / CH2Cl2 13. H...
OH OH B no Give the proper reagent (from the table below) that will carry out the transformation shown for each step. (Assume aqueous workup where needed.) 1. Cl2 / uv light 2. Br2 / uv light 3. Mg/Et20 4. Li metal/hexane 5. propanal 6. PBr3/THE 7. CrO3/THF 8. PCC / CH2Cl2 9. CH3CH2CH2MgCl 10. NaBH4 11. acetone 12. OH 13. H7H20 14. BH3 / ox 15. t.butoxide 16. PhMgBr Enter a number, 1 through 16, for each answer. Step...
MgCl Ph Ph Give the proper reagent (from the table below) that will carry out the transformation shown in three steps. (Assume aqueous workup where needed.) 1. Cl2 / uv light 2. Br2 / uv light 3. Mg / Et20 4. Li metal/ hexane 5. H2C-O 9. CH3CH2MgCI 10. LiAIH4 13. Ht /H20 14. BH3/ox 15. H2/Ra Ni 16. PhMgBr 6. PBr3/THF 7. CrO3/THF 8. PCC/ CH2CI2 11. TMS-cl/R3Nİ 12. SOCb Enter a number, 1 through 16, for each answer...
Multi-step synthesis ci R R NH, OEt А OH B 1. Br2 / uv light 2. SOCI2 / THE 3. Mg/Et20 4. Meu/hexane S. CH3CH2MgCl 6. Ph MgBe 7. NaBHA 8. LAHA 9. BH3 /OX 10. POCl/pyridine/ THF 11.03/THE 12. PCC / CH2 13.H/H20 14. ELOH/H 15. t-butaxide 16. OH/H20 17. NHS 18.CO2 19. acetic anhydride 20.HNMez/THE In each box, type out the list of reagents in proper order that will carry out the synthesis of the final product (This...
Propose an efficient synthesis for the transformation below. Enter the appropriate number of letter from the reagent list handout Step 1 Step 2 Step 3 OH Alkyl Halides (X = CI, Br or 1) and Acyl chlorides: Assume Allig 15 present, if needed CIP CU CH3X X CI E A B EE Ketones. Aldehydes and Epoxides: Assume "then H20" is included if a protonation step is needed F A A K 0 MN Р Grignard, Wittig and Organocuprate Reagents: Assume...
Propose an efficient synthesis for the transformation below,
using two sequential reductive aminations. Enter
the appropriate number or letter from the reagent list handout.
Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number or letter from the reagent list handout. Step 1 + NaBH3CN, H+, Step 2 - NaBH3CN, H+ Reagent List (Updated 4/30/2020) Enter # or letter in the appropriate boxes. Note: Exam responses are case insensitive Alkyl Halides (X = Cl,...
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