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18.-22. Starting with benzene, what is the major product of each reaction sequence?...
15.-19. Starting with benzene, match each sequence of reagents (separated by commas) to a major product....
15.-19. Starting with benzene, match each sequence of reagents (separated by commas) to a major product. Answers may be repeated. Assume any necessary workup. 15 AICI, Bro/FeBr Br 16. 6 /AlCI3, Zn/HC, HNO3/H2S04, H2/Pd, NaNO2/HCI/O C, CuBr b. /AlCl3, Br2/FeBr3, N2Ha/KOH/heat C. Br Br 18. /AlCl3, HS(CH2)2SH/H+, H2/Ni, H2S04, Br2/FeBr3, H2O/heat d. 19. /AICls, HNO:/H S04, H2/Pd, Bra/FeBr3, NaNO/HCI/o'C, H3PO2 e.not a.-d
DOME 4. What will be the best way to synthesize the following compound starting from benzene?...
DOME 4. What will be the best way to synthesize the following compound starting from benzene? the o ů na A. 1) CH3CH2CI, AICI3; 2) Cl2, FeCl3 B. 1) CH2=CH2, HF; 2) Cl2, FeCl3; ovods and to none C. 1) CH3CO-O-COCH3, AICI3; 2) Cl2, FeCl3; 3) Zn, HCI; D. 1) CH3CO-O-COCH3, AICI3; 2) Zn, HCI; 3) Cl2, FeCl3; E. none of the above EVE. none droedsw abruogo Oriollot to 8 Smund og tengsmont to 5. What set of reagents will...
could someone please answer these 3 questions? 2. What product would you expect from the following...
could someone please answer these 3
questions?
2. What product would you expect from the following reaction? ÇOCH B ÇOCH A oi CO2CH3 B ÇOCH E. CO2CH3 4. What will be the best way to synthesize the following compound starting from benzene? D CO2CH3 8 E A. 1) CH3CH2CI, AICI3; 2) Cl2, FeCl3 B. 1) CH2=CH2, HF; 2) Cl2, FeCl3; C. 1) CH3CO-O-COCH3, AICI3; 2) Cl2, FeCl3; 3) Zn, HCI; D. 1) CH3CO-O-COCH3, AICI; 2) Zn, HCI; 3) Cl2, FeCls;...
Please help with 21-25 and explain the answers! 21.-25. Starting with benzene, match each reaction sequence...
Please help with 21-25 and explain the answers!
21.-25. Starting with benzene, match each reaction sequence to a product on the right. Assume any necessary workup. Answers may be repeated. 21. Br/FeBr, a. b. C. , Br/FeBr, HS(CH),SH/HCI, H/Ni d. 25.Zn/HCI, HNO/H.SO, Br/FeBr, H/Pd, NaNO/HCl/cold, H,PO e. not a.-d.
Which of following is the best starting material for the reaction below? 1. (CH3)2NH ? 2....
Which of following is the best starting material for the reaction below? 1. (CH3)2NH ? 2. LIAIHA 3. H20 'N NK CN NH2 What is the major product in the following reaction? 1. DIBAL 2. H20 O H O OH OH СІ Which reaction sequence would accomplish this transformation? CN H2SO4/HNO3 Br2 NaNO2/HCI CuCN O Br2/FeBr3 H2SO4/HNO3 KF NaNO2/HCI O H2SO4/HNO3 Zn(Hg)/HCI NaNO2/HCI CuCN o H2SO4/HNO3 Zn(Hg/HCI NaNO2/HCI HBF4
1. What is the major product of the following sequence of reactions? a. 1. Li 1....
1. What is the major product of the following sequence of reactions? a. 1. Li 1. 2. Cu 2. H20 b. H2 (1 equiv. Pd(s) Which of the reaction conditions would accomplish this transformation? 2. A. 1 . CH3SH (excess), H' 2. Raney Ni B. . H2NNH2 2. HO, H2O/A Zn, HCI acetic acid / Δ None of these C. D.
please help in all sections asap!! Provide the reagents necessary to carry out the following conversion....
please help in all sections asap!!
Provide the reagents necessary to carry out the following conversion. ОСН Br Br NO2 Choose the correct reagents for step 1 fuming H2SO4 HNO3/H2S04 excess Br2/ FeBr3 dilute H2SO4 O Cl2/FeCly O CH3ONA Choose the correct reagents for step 2. Cl2/ FeCl3 HNO3/H2SO4 CH3ONA fuming H2SO4 excess Br2/ FeBr3 dilute H2SO4 Choose the correct reagents for step 3 CH3ONA HNO3/ H2SO4 O excess Br2/ FeBr3 Odilute H2S04 fuming H2SO C2/ FeCl Choose the correct...
Using the reagents listed below, propose a synthesis of the target compound starting from benzene. Assume...
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
9. Draw the molecules formed after each step in the following sequence. 1) HNO3, H2SO4 2)...
9. Draw the molecules formed after each step in the following sequence. 1) HNO3, H2SO4 2) Cl2, FeCl3 3) Fe, HCI 4) NaNO2, H2SO4 5) H20, A
What is the major organic product of the following reaction sequence? Type its systematic IUPAC name...
What is the major organic product of the following reaction sequence? Type its systematic IUPAC name in the box below. 1) HNO3, H2SO4 2) Sn, HCI 3) NaNO2, HCI, O °C 4) CuCN 5) H2SO4, H20, heat
15.-19. Starting with benzene, match each sequence of reagents (separated by commas) to a major product. Answers may be repeated. Assume any necessary workup. 15 AICI, Bro/FeBr Br 16. 6 /AlCI3, Zn/HC, HNO3/H2S04, H2/Pd, NaNO2/HCI/O C, CuBr b. /AlCl3, Br2/FeBr3, N2Ha/KOH/heat C. Br Br 18. /AlCl3, HS(CH2)2SH/H+, H2/Ni, H2S04, Br2/FeBr3, H2O/heat d. 19. /AICls, HNO:/H S04, H2/Pd, Bra/FeBr3, NaNO/HCI/o'C, H3PO2 e.not a.-d
DOME 4. What will be the best way to synthesize the following compound starting from benzene? the o ů na A. 1) CH3CH2CI, AICI3; 2) Cl2, FeCl3 B. 1) CH2=CH2, HF; 2) Cl2, FeCl3; ovods and to none C. 1) CH3CO-O-COCH3, AICI3; 2) Cl2, FeCl3; 3) Zn, HCI; D. 1) CH3CO-O-COCH3, AICI3; 2) Zn, HCI; 3) Cl2, FeCl3; E. none of the above EVE. none droedsw abruogo Oriollot to 8 Smund og tengsmont to 5. What set of reagents will...
could someone please answer these 3
questions?
2. What product would you expect from the following reaction? ÇOCH B ÇOCH A oi CO2CH3 B ÇOCH E. CO2CH3 4. What will be the best way to synthesize the following compound starting from benzene? D CO2CH3 8 E A. 1) CH3CH2CI, AICI3; 2) Cl2, FeCl3 B. 1) CH2=CH2, HF; 2) Cl2, FeCl3; C. 1) CH3CO-O-COCH3, AICI3; 2) Cl2, FeCl3; 3) Zn, HCI; D. 1) CH3CO-O-COCH3, AICI; 2) Zn, HCI; 3) Cl2, FeCls;...
Please help with 21-25 and explain the answers!
21.-25. Starting with benzene, match each reaction sequence to a product on the right. Assume any necessary workup. Answers may be repeated. 21. Br/FeBr, a. b. C. , Br/FeBr, HS(CH),SH/HCI, H/Ni d. 25.Zn/HCI, HNO/H.SO, Br/FeBr, H/Pd, NaNO/HCl/cold, H,PO e. not a.-d.
Which of following is the best starting material for the reaction below? 1. (CH3)2NH ? 2. LIAIHA 3. H20 'N NK CN NH2 What is the major product in the following reaction? 1. DIBAL 2. H20 O H O OH OH СІ Which reaction sequence would accomplish this transformation? CN H2SO4/HNO3 Br2 NaNO2/HCI CuCN O Br2/FeBr3 H2SO4/HNO3 KF NaNO2/HCI O H2SO4/HNO3 Zn(Hg)/HCI NaNO2/HCI CuCN o H2SO4/HNO3 Zn(Hg/HCI NaNO2/HCI HBF4
1. What is the major product of the following sequence of reactions? a. 1. Li 1. 2. Cu 2. H20 b. H2 (1 equiv. Pd(s) Which of the reaction conditions would accomplish this transformation? 2. A. 1 . CH3SH (excess), H' 2. Raney Ni B. . H2NNH2 2. HO, H2O/A Zn, HCI acetic acid / Δ None of these C. D.
please help in all sections asap!!
Provide the reagents necessary to carry out the following conversion. ОСН Br Br NO2 Choose the correct reagents for step 1 fuming H2SO4 HNO3/H2S04 excess Br2/ FeBr3 dilute H2SO4 O Cl2/FeCly O CH3ONA Choose the correct reagents for step 2. Cl2/ FeCl3 HNO3/H2SO4 CH3ONA fuming H2SO4 excess Br2/ FeBr3 dilute H2SO4 Choose the correct reagents for step 3 CH3ONA HNO3/ H2SO4 O excess Br2/ FeBr3 Odilute H2S04 fuming H2SO C2/ FeCl Choose the correct...
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
9. Draw the molecules formed after each step in the following sequence. 1) HNO3, H2SO4 2) Cl2, FeCl3 3) Fe, HCI 4) NaNO2, H2SO4 5) H20, A
What is the major organic product of the following reaction sequence? Type its systematic IUPAC name in the box below. 1) HNO3, H2SO4 2) Sn, HCI 3) NaNO2, HCI, O °C 4) CuCN 5) H2SO4, H20, heat
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