HNO, H,SO AICI, H2SO4 Fuming H2SO4 HO/HASO, HgSO4 2) HO excess Excess BryFeBig Na(s) NHEID CHCHOH...
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
19. Which would be the reagent in the reaction shown? H₂ Na, NH3 Твн then H2O2, HO PtO2 HO, H2SO4 HgSO4 d But why?
CH, Bre, light CI 1 Brz, AIBr; A B AICI HNO, c CO, HCI; Cuci, AICI3 H2SO4 D CH3 HNO3, H2SO4 H F Br SO; H2SO4 G E CO2 I со, A= B= C= D= E= F= G= H= Which reaction sequence best accomplishes this transformation: NO2 SOZH OCH3 Br OCHZ You a) SO3 H2SO4 Pd(OAC)2 HNO, H2SO4 AICI (HO)2B OCH b) HNO3 H2SO4 SO3 H2SO4 Br2 AICI: Pd(OAc)2, base (HO),B. OCH3 c) Zn(Hg) HCI, H20 HNO3 H2SO4 SO, H2SO4...
(a) 2 1. -OH, H2O H 2.H307, heat (b) CI AICI: (c) SH HS H2SO4 (d) OH 1. Na Cr 07, H2SO4 2. SOCl2, pyridine 3. excess (CH2CH2)2NH excess (e) (f) Br2, H30*
predict all products
HO CHCHOH Sul СОН Na. Co -OH HI H,SO PCC mem он он Jones Nal NaOH NaOH, CH3OH -S2 ch - e-cly of c...d- S,2 thy s CH E1 КОН Ethanol
7. You think organic synthesis is a headache? Why not make some aspirin? Starting from phenol, how would synthesize the product with the given list of chemicals below. (5 pts) There is more than one way to do this. Do worry about specific solvent conditions only reagent conditions you List of reagents: HO Ethanol Methanol Actone HC H,SO, (fuming) H,SO HNO NaOH NH, NaNH Phenol Aspirin Jones Reagent mCPBA NHNH2 SOC LiAIH Zn Hg Pyridine TMSC NaBH Lindlars Catalyst Pd...
aromatic reactivity mechanisms not needed only products
Draw the product(s) of the following reactions HNO/H,SO AICI SOY/H2SO4 Bry/FeBry HNO/H,80 AICI Bry/FeBry
Draw the product(s) of the following reactions HNO,/H2SO а. Br b. AICI он So/H2SO C. Он Br/FeBr3 d. HNO3/H2SO4 Br e. OCH3 H3CO. f. AICI OCH3 но g. AICI NO3 Bro/FeBr3 h.
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...
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...