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10 dd.) Br XS NBS CCL, A C Br ee. S0₂H 1. fuming H2SO4 2. HNO/H2SO4...
dd.) XS NBS CCM, A ee.) 1. fuming H2SO4 2. HNO3/H2SO4 3. Zn(Hg), HCI, A ff.) OH 1. H.Cros/acetone 2. PrMgl/Et20 3. H30* gg.) HORS. NH2 SO3 H2SO4 hh.) OE 1. LAIH/Et20/ -78 °C 2. H20 ii.) 1. Li/Et, 2. Ph Co 3. H30* jj.) Br 1. Mg/THE 2. formaldehyde 3. NHCl(aq) kk.) 2 Na, EtOH, NH3 II.) CH3BF4 mm.) SOUH 2 Na, EtOH, NH3 nn.) NO2 H2SO4(conc) HNO3(conc) NO2 00.) 1. SO3, H2SO4 2. NaOH/KOHA 3. H30*
Please include any enantiomers! 10 dd.) XS NBS Сclu, A ee.) Sogh 1. fuming H, SO 2. HNO3/H,804 3. Zn(Hg), HCI, A ff.) OH 1. H.CO/acctone 2. Prieto 3. H30 99.) HOGS NH SO3 H2SO4 hh.) OET 1. LAH/Et20/-78 °C 2. H20 ii.) CI 1. LIETO 2. Ph.co 3.5
a.) H H_Cro acetone b.) 1. XS KMnO,/KOH/HOIA 2.H30* c.) ni XS NaBH,, H,0 H OH d.) o 1. XS LAIH/THF/-78 °C 2. H20 H OH e.) NaNH / lig NH3 f.) Br 1. Mg/THE 2. CO2 3. H30 9.) Ph Ph cyclopropene HF CH h.) OH 1. PCCICH.CH 2. Pri 3. N,Cag) 1. LITHF 2.CO 3. NH.Ca) HNO, NH 1. HNO () 2. NaSCH CH.CH AICI, 3-chloro-2-methylpentane m.) 1.Pr.CI. AICI 2. NBS, CCH n.) OH XS H.COM acetone OH...
Ph cyclopropene HF CH h) OH 1. POCICH.Ch 2. Pri 3 NH4Cl ag) 1.) 1. Li/THE 2.CO 3.NH.CH HNO k.) NH 1. HNO (aq) 2. NaSCH CH.CH AICI, 3-chloro-2-methylpentane m.) 1.Pr.CI. AICI 2. NBS, CCU. n) -OH XS H.CO acetone он 0.) OH XS Bobbit's SiO, CH.CH -OH 1. Ch. AICI 2 NaOH, 30 C 4,000 psi 3. HCI 9.) SCH 2Na, ETOH, NH, r.) 1. LIETO 2. oxirane 3. H,00 1.2 PY-MOBI OMe 2. NHCl(aq) t.) 1. Cl/ Feer...
please include any enantiomers! a.) H H2Cr04 acetone b.) 1. XS KMnO4/KOH / H2O/A 2. H30* c.) XS NaBH4, H20 H OH d.) 1. XS LIAIH/THF/-78 °C 2. H20 OH H e.) NaNH / liq NH3 f.) Br 1. Mg/THE 2. CO2 3. H30* Ph Ph cyclopropene HF CHE h.) OH 1. PCC/CH2CH2 2. i-PrLi 3. NH4Cl(aq) i.) CI 1. LITHF 2. CO2 3. NHCl(aq) j.) Ph 1/HNO, Ph k.) NH2 1. HNO,(aq) 2. NaSCH2CH2CH3 1.) AICI: 3-chloro-2-methylpentane
provide the major product in the following reactions ОН TsCI O Et N NH2 1. CHg-Br (xs) 2. Ag2O, H20, A H-CI Et20
NO, 00) 1.80.H.SO 2 онкона 3.HO pp.) 2 Na NDIO 1.2.2,0 2 DO XS PCC HO CH ON OH XSHCIO NH إياها NINH w.) OH OH XS Bobbitt's SiO, CH2Cl2 ww.) OH 1. XS KMnONaOH(aq). A 2. H,O* HO 1. NaNO.HCI 2. H,PO (a) CHO NH yy.) NH 1. NaNO, HCl(conc) 2. D.PO 1. LITHF 2. D20 14 aaa) wo NaBHJEICH bbb.) су Cl2 FeBry HO НО. Feb COL) H 1 KM. NOW 2. Ho didd) cleum com) NO 1....
hh.) OEt 1. LIAIHJE!,0/-78 °C 2. H,0 1. LIELO 2. Ph.CO 3.H30 Br 1. Mg/THF 2. formaldehyde 3. NHCl(aq) kk.) 2 Na, EtOH, NH CH,BF mm.) SOH 2 Na, EtOH, NH, nn.) NOZ H2SO4(conc) HNO3(conc) NO 00.) 1. SO, H,SO 2. NaOH/KOHA 3. H,0*
please help! will give rating. thank you! L. 1.CH,Br 2. H,0 M. NaBH CH, OH 0. Brz P. Hz, Pd N. 1. KCN 2. LIAIHA 3. H2O ОН Q. NaOH, Bra B. 1, KCN 2. HCI 3. cat NaOH H2O S. NHA mild H+ I. NH3 NaBH3CN U. 1. CHgMgBr 2. H2O, H Determine the reagents necessary to carry out each of the following transformations. The reagent choices are listed in the text box above this question (reagents L-U). You...
833 17-10 The Friedel-Crafts Alkylation 1.2NaOH 100 °C 2. H,09 o Zn(Hg) dilute HCI NBS hy NO, Zn HCI C 17-10 The Friedel-Crafts Alkylation U 8. Predict the major product or products for the following reactions. Assume reagents are present in excess amounts unless otherwise indicated. Clearly depict any stereochemistry. "No Reaction is a possible answer. (4 points) each et :O 1 SO, H2SO4 CH2 CH3 сH,CH,CI AICI, NO2 Br FeBrz OH AICI 1 cq Bry FeBr