Aromatic electrophilc substitution reaction.
dd.) XS NBS CCM, A ee.) 1. fuming H2SO4 2. HNO3/H2SO4 3. Zn(Hg), HCI, A ff.)...
please include any enantiomers! 11 Br 1. Mg/THF 2. formaldehyde 3. NH4Cl(aq) kk.) 2 Na, EtOH, NH3 II.) CH3BF4 mm.) SO3H 2 Na, EtOH, NH3 nn.) NO₂ -NO₂ ii2SO.(conc) HNOs(conc) No 2 NO2 oo.) 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
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*
10 dd.) Br XS NBS CCL, A C Br ee. S0₂H 1. fuming H2SO4 2. HNO/H2SO4 3. Zn(Hg). HCI, A u ff.) OH HO ,Ph 1. H.CrO lacetone 2. PrMgl/Et20 3. H2O* gg.) HO3S. NH2 SQ3H -NH2 SO, H2SO4 303H hh.) OEt -CH₂-OH 1. LiAlH./Et20/ -78 °C 2. H2O il.) Ph Ph 1. Li/Et, 2. Ph Co 3. H,0 Pn
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...
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....
1. Predict the major product(s) for the following reactions. (18 points) NO2 HNO3 H2SO4 Na NH3 CH3CH OH 1. KMnO4 H20 Heat 2. H2O SO3 H2SO4 Pd(OAC) PPh3 NET 3 Cl2 AICI3
1)? 2) ? 3) ? 12? NO2 Choose from the following list of reagents. KMnO4, NaOH, heat Br2 Fuming H2SO4 H30+ H Excess NBS Zn, HCI HNO3, H2SO4 Zn(Hg), HCI, heat Enter the correct letter for each step of the reaction in the boxes below. (Reagents cannot be used more than once) Reagent 1: Reagent 2: Reagent 3:
1. Draw the product(s) of the following reactions HeCrO4 1. CH,COCVAICI 2. Zn (Hg)HCI 3. NBS (light) 1. KMnO4/H2SO4 og er CH3 NaNH2 NH3(0) 2. Show how you would synthesize the following compounds from toluene. OH O он Br