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h. and i. Starting with benzene how would you synthesize j.+k. Starting with benzene how would...
Practice Problem 22.68b Starting with benzene, show how you would prepare the following compound: NH2 NH2...
Practice Problem 22.68b Starting with benzene, show how you would prepare the following compound: NH2 NH2 cl 1) HNO3, H2SO4 2)? Compound A Cla 3)? 4) ? 5) H30* Choose from the following list of reagents: A B с D Fe, H3O+ CuCN LDA H30+ E F G H NaOH, heat NaOEt/EtOH H20 HCI, Zn[Hg), heat J K L CO2 NaNH2, NH3 [H] NaBH3CN NaNO2 HCI
17. Use ANY needed reagents to effect the following transformation. (30 points) starting material product List...
17. Use ANY needed reagents to effect the following transformation. (30 points) starting material product List of Reagents -N:C:N- KMnO4, H2SO4 8 00 (CH3),COCOCOC(CH3)3 Ag(NH3)2+, 120 Fe, HCI KMnO4, NaOH, H2O, cold AlCl3 Bra (excess), NaOH (excess), H20 Brz, Fe Br2, H20 Br2, H2O, H3O+ Br2, hy Br2, NaOH (excess), H2O Br2, P Buli CF3CO,H CH;=0 Formaldehyde оо CH3COCCH o CH_CC1, pyridine H2, Lindlar's catalyst H2.Pd/C H2, Pa/C, high pressure H, Raney-Ni HANNH HENNH, KOH, (HOCH2CH2)20, heat H2O H20, H2SO4,...
Synthesis of target compound starting from benzene. Assume all reactions are appropriately worked up and that...
Synthesis of target compound starting from benzene. Assume all
reactions are appropriately worked up and that mixtures of
constitutional isomers can be separated. May use a reagent more
than once if needed.
A. Cly/FeCl3 B. HNO3/H2SO4 C. CH3COCI/AICI: D. NaNO/HCI E. HC1/Cuci F. KCN/CuCN G. H3PO2 H. H2O/heat I. H2Cr04 J. 1)LiAlH42)H2O 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 -NH₂ CI
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
using the word bank below, propose a synthesis of the target compound starting from benzene. Using...
using the word bank below, propose a synthesis of the target
compound starting from benzene.
Using the reagents listed below, propose a sythesis of the target compound starting from benzene. wish to use them. You may assume that all reactions are appropriately worked up and that mixture NH2 A. Cl/FeCl3 B. HNO3/H_SO4 C. CHCOCI/AICI: D. NaNO_/HCI E. HC1/Cuci F KCN/CuCN G. H2PO2 H. H2O/heat I. H Cr04 J. 1)LiAlH4 2)H2O K. H /Ni L. 1) Mg 2)C02 3)H30+ M. CH3OH/H30+...
Starting with benzene as your only source of aromatic compounds, how would you synthesize the following...
Starting with benzene as your only source of aromatic compounds, how would you synthesize the following substances? Assume that you can separate ortho and para isomers if necessary. p-Chlorotoluene m-Bromonitrobenzene o-Bromobenzenesulfonic acid m-Chlorobenzenesulfonic acid Starting with either benzene, phenol, or toluene, how would you synthesize the following substances? Assume that ortho and para isomers can be separated 2-Bromo-4-methylphenol 1,3,5-Trinitrobenzene 2,4,6-Tribromoaniline 2-Chloro-4-nitrotoluene
Starting with Benzene, propose a synthesis for this reaction. CI CI OH A. Cl/FeCl3 B. HNO3...
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
Starting with benzene, how would you synthesize the following products? You can use any chemical you...
Starting with benzene, how would you synthesize the following
products? You can use any chemical you can find from chapter 7- 13,
or 16-18 to help you in your synthesis. (15 pts, 5 points
each)
3. Starting with benzene, how would you synthesize the following products? You can use any chemical you can find from chapter 7-13, or 16-18 to help you in your synthesis. (15 pts, 5 points each) OH o-bo
sbow how you woukd synthesize each of the following compounds from benzene (a) Show how you...
sbow how you woukd synthesize each of the following compounds from
benzene
(a) Show how you would synthesize each of the following compounds from benzene. Br (b) (c) (d) NHA Br. Br. (e) HN NH2
Problem #3 Show how you would synthesize ethyl benzoate in good yield starting from benzene. You...
Problem #3 Show how you would synthesize ethyl benzoate in good yield starting from benzene. You may use any other reagent necessary
Practice Problem 22.68b Starting with benzene, show how you would prepare the following compound: NH2 NH2 cl 1) HNO3, H2SO4 2)? Compound A Cla 3)? 4) ? 5) H30* Choose from the following list of reagents: A B с D Fe, H3O+ CuCN LDA H30+ E F G H NaOH, heat NaOEt/EtOH H20 HCI, Zn[Hg), heat J K L CO2 NaNH2, NH3 [H] NaBH3CN NaNO2 HCI
17. Use ANY needed reagents to effect the following transformation. (30 points) starting material product List of Reagents -N:C:N- KMnO4, H2SO4 8 00 (CH3),COCOCOC(CH3)3 Ag(NH3)2+, 120 Fe, HCI KMnO4, NaOH, H2O, cold AlCl3 Bra (excess), NaOH (excess), H20 Brz, Fe Br2, H20 Br2, H2O, H3O+ Br2, hy Br2, NaOH (excess), H2O Br2, P Buli CF3CO,H CH;=0 Formaldehyde оо CH3COCCH o CH_CC1, pyridine H2, Lindlar's catalyst H2.Pd/C H2, Pa/C, high pressure H, Raney-Ni HANNH HENNH, KOH, (HOCH2CH2)20, heat H2O H20, H2SO4,...
Synthesis of target compound starting from benzene. Assume all
reactions are appropriately worked up and that mixtures of
constitutional isomers can be separated. May use a reagent more
than once if needed.
A. Cly/FeCl3 B. HNO3/H2SO4 C. CH3COCI/AICI: D. NaNO/HCI E. HC1/Cuci F. KCN/CuCN G. H3PO2 H. H2O/heat I. H2Cr04 J. 1)LiAlH42)H2O 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 -NH₂ CI
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
using the word bank below, propose a synthesis of the target
compound starting from benzene.
Using the reagents listed below, propose a sythesis of the target compound starting from benzene. wish to use them. You may assume that all reactions are appropriately worked up and that mixture NH2 A. Cl/FeCl3 B. HNO3/H_SO4 C. CHCOCI/AICI: D. NaNO_/HCI E. HC1/Cuci F KCN/CuCN G. H2PO2 H. H2O/heat I. H Cr04 J. 1)LiAlH4 2)H2O K. H /Ni L. 1) Mg 2)C02 3)H30+ M. CH3OH/H30+...
Starting with benzene as your only source of aromatic compounds, how would you synthesize the following substances? Assume that you can separate ortho and para isomers if necessary. p-Chlorotoluene m-Bromonitrobenzene o-Bromobenzenesulfonic acid m-Chlorobenzenesulfonic acid Starting with either benzene, phenol, or toluene, how would you synthesize the following substances? Assume that ortho and para isomers can be separated 2-Bromo-4-methylphenol 1,3,5-Trinitrobenzene 2,4,6-Tribromoaniline 2-Chloro-4-nitrotoluene
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
Starting with benzene, how would you synthesize the following
products? You can use any chemical you can find from chapter 7- 13,
or 16-18 to help you in your synthesis. (15 pts, 5 points
each)
3. Starting with benzene, how would you synthesize the following products? You can use any chemical you can find from chapter 7-13, or 16-18 to help you in your synthesis. (15 pts, 5 points each) OH o-bo
sbow how you woukd synthesize each of the following compounds from
benzene
(a) Show how you would synthesize each of the following compounds from benzene. Br (b) (c) (d) NHA Br. Br. (e) HN NH2
Problem #3 Show how you would synthesize ethyl benzoate in good yield starting from benzene. You may use any other reagent necessary
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