We need at least 10 more requests to produce the answer.
0 / 10 have requested this problem solution
The more requests, the faster the answer.
Write complete equations (using structures) to the following sequence of reactions and give the structures of...
Write complete equations (using structures) to the following sequence of reactions and give the structures of compounds A through I. Neatness counts B AICI, HNO H2SO4 Zn(Hg) HCI KMnO с (hot, coned.) D NH BIZ NH, hv (CH3),COK E Heat NaOCH Cyclopentadiene/Heat G H F
Write complete equations (using structures) to the following sequence of reactions and give the structures of compounds A through I. Neatness counts B AICI, HNO3 A H2SO4 Zn(Hg) HCI KMnO4 с (hot, concd.) D NH, Br₂ hv NH (CH),COK Heat Cyclopentadiene/Heat G H E | NaOCH F Write complete equations (use structures) for each of the following conversions. Include appropriate reagents.
Write complete equations (using structures) to the following sequence of reactions and give the structures of compounds A through 1. Neatness counts B AICI, D ΗΝΟ, H,SO Za(Hg) HCI KMnO с hot, concd.) Brz (CH),COK E Heat NaOCH, NH NH Cyclopentadiene/Heat G F Write complete equations (use structures) for each of the following conversions. Include appropriate reagents. Benzene -> A A-> Ac C->D C->E E->G G-> E-> F E-> 1 => React with (CH.CO),0, N(C2Hs)
Question 1: [14 points] Write complete equations to the following sequence of reactions and give the structures of compounds A through I. Neatness counts Cl HNO AICI H So Zn(Hg) HCI KMnO (hot, concd.) NH (excess) (CH3CO K HBr NaOCH, Write complete equations for each of the following conversions. Include appropriate reagents Benzene -> A This reaction is (circle one) Addition, substitution, oxidation, elimination, or none A -> B This reaction is (circle one) Addition, substitution, oxidation, elimination or none...
6. (10 points) Give the structures of compounds A through Hin the following series of reactions. Mgi AICI Zn(Hg) HCI с KMnO4 (Hot and conc.) 1. LIAIHA 2. H,0 E Br/hv NH2 (CH3),COK NH3 (excess) 1. m-CPBA H 2. CH3MgBr Br2 NaNH2 J (2 equiv)
HNO Cl AlCI H,so, Zn(Hg) HCl KMnO (hot, concd.) HBr (CH3)CO K+ NH3 (excess) NaOCH3 Write complete equations for each of the following conversions. Include appropriate reagents.
1. Provide the major organic product(s) for each of the following reactions: 1) HNOZ/H, SO 2) Sn/HCl(aq) 3) HO 1) (CH3)2CHCI/AICI: 2) NBS/hv 1) Cly/FeCl3 2) HNO,/H2SO4 1) CH3CH,COCI/AICI 2) H20 оооооооо 3) Zn(Hg)/HCl(aq) 1) SOZ/H,SO 2) Bry/FeBrz 1) (CH3)3CCI/AICI: 2) KMnO/HOIA 2) H30* 1) CH,COCIAICI: 2) H, 3) Bry/FeBry COH 1) SOCI_/pyridine 2) PhCH/AICI 3) H20 1. Br JFeBry 2. Mg/Eto 3. oxirane 4, HO* 1) Bry/FeBry 2) s09/H230 1) NBS/hv 2) PhoNa (1 CH3COCI / AIC وا (2...
Give the product structures throughout the scheme, from A to I. Follow the series of reactions. Show product of this nucleophilic aromatic substitution reaction. Provide how a Diels Alder reaction would perform on this compound. Thanks so much 1) (27 points) Give the structures of compounds A through I in the following series of reactions CHE Brz, light CI Brz, AIBry AICI CO, HCI; CUCI, AICI3 HNO, H2SO4 D HNO,, H2SO4 сн. Br H F SO, H2SO4 CO, CO, A-...
Study Pr 3 Predict the major products of the following reactions. (a) 2,4-dinitrochlorobenzene + NaOCH3 (c) nitrobenzene + fuming sulfuric acid (e) p-methylanisole + acetyl chloride AICI, (g) 1,2-dichloro-4-nitrobenzene NaNH2 (i) p-ethyibenzenesulfonic acid +steam/H (b) phenol + tert-butyl chloride + AICl, (d) nitrobenzene + acetyl chloride +AlC1 (f) p-methylanisole + Br2, light (h) p-nitrotoluene + Zn + dilute HCl j) p-ethylbenzenesulfonic acid + HNO3, H2S + hot, concd. KMnO Ph-C-NHPh + CH,CH,-C-CI, AICI3 indane Study Pr 3 Predict the major...
7. Complete the following transformations by drawing the structures of the organic products PhLi H,o heat H2-Pd/C HNo, H2O, acetic H2SO4 acid heat Br2, FeBr3 NaNO2 NH, H 2 heat HBF NaNO heat N NH, HCI H2o KNH2 N heat 7. Complete the following transformations by drawing the structures of the organic products PhLi H,o heat H2-Pd/C HNo, H2O, acetic H2SO4 acid heat Br2, FeBr3 NaNO2 NH, H 2 heat HBF NaNO heat N NH, HCI H2o KNH2 N heat