6. Provide the most efficient synthesis possible by matching the reagents to the reaction. Write the...
Ochem 2 ch 22 Ch 22 Amines (100 pts) Chemistry 2320 p) H&NO3/H2SO 1) Fe, HCI 2) NaOH H2N 1) H2NOg/H,SOA CUCN 2) NaNO2 H2SO4 г) 1) NaNO2 H2SO4 1) H2NO3/H2SO4 2) Fe, HCI 2) HBF4 6. Provide the most efficient synthesis possible by matching the reagents to the reaction. Write the letter(s) over or adjacent to the corresponding reaction arrow. As many as three steps represented by each letter may be needed. Assume intermediate products are isolated and purified...
Provide the most efficient synthesis possible by matching the reagents to the reaction. Write the letter(s) over or adjacent to the corresponding reaction arrow. As many as three steps represented by each letter may be needed. Assume intermediate products are isolated and purified or used in situ as appropriate. B. HN(CH3)2, H C. NaCrO1, H>SO,Ph D. CH3MgBr, Et2O E. HCN F. LiAlH, THF G. H2CP(Ph) H H2SO, heat I. OsO4 J. Mg, Et,20 K. H2NOH, H OH Ph Ph CN...
Chemistry 2320 Ch 18 Aldehydes and Ketones (100 pts) 3. Provide the most efficient synthesis possible by matching the reagents to the reaction. Write the letter (3) over or adjacent to the corresponding reaction arrow. As many as three steps represented by each letter may be needed. Assume intermediate products are isolated and purified or used in situ as appropriate. A. HOVOH B. HN(CH3)2, H' OH XCN C. Na2Cr2O, H2SO4 LOH Ph D. CH,MgBr, Eto E. HCN F. LiAIH, THE...
Using the reagents listed below, propose a synthesis of the target compound starting from benzene. Assume all reactions are appropriately worked up and that mixture of constitutional isomers can be separated. CI NH2 A. Cl/FeCl3 B. HNO3/H2SO4 C. CH3COCI/AICI: D. NaNO2/HCI E. HC1/Cuci F. KCN/CuCN G. H3PO2 H. H2O/heat I. H Cr04 J. 1)LiAlH4 2)H20 K. H/Ni L. 1) Mg 2)CO2 3)H30 M. CH3OH/H30+ N. (CH3)2SO4 NaOH O. CH3OH SOCI Q. HCI R. NaN3
What are the steps that give this product given the reagent list. Multistop Synthesis NH₂ A. Cl2/FeCl3 B. HNO3/H2SO4 C. CH3COCI/AICI: D. NaNO2/HCI E. HC1/Cuci F, KCN/CuCN G. H3PO2 H. H2O/heat I. H Cr04 J. 1)LiAlH4 2)H20 K. H/Ni L. 1) Mg 2)CO2 3)H30 M. CH3OH/H30* N. (CH3)2SO4 NaOH 0. CH3OH P. SOCl2 Q. HC1 R. NaN3
Starting with Benzene, propose a synthesis for this reaction. CI CI OH A. Cl/FeCl3 B. HNO3 H2SO4 C. CH3COCI/AICI: D. NaNO/HCI E. HC1/Cuci F KCN/CuCN G. H3PO2 H. H2O/heat I. H_CrO4 J. 1)LiAlHA 2)H2O K. H/Ni L. 1) Mg 2)CO2 3)H30+ M. CH2OH/H30+ N. (CH3)2SO4 NaOH O. CH3OH P. SOCI2 Q. HC1 R NaN3
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,...