Mg, ether 1-bromobutane. (D) KOH, H2O (A) Na (B) CH CH Br (C) (i) CH30CH2 3...
1) + NaOH J) PCC OH CHCI K) H CH OH L) 1. Mg, ether Br 2. 3. H2O M) OH I Na Cr2O7 H2SO4
For each reacuon ere s only as an aid for you. 1) KOH, H-O, heat Diethyl malonate B 1) Ph3P, ether 2) nBuLi, ether CIH1204 2) H, H2O, heat C1SH2406 CHH1202 NaOEt, EtOH Br OCH2CH3 3) PHCHO NH/heat Note: The C-13 NMRS for Structures C, D, and E each show 7 resonances LIAIH D E C1HNO ether C1H1SN Br 1) SOCI2, pyridine F 2) CH3OH 1) CH2COCI,AICI3 1) Mg(s), Et20 H 2) diisopropyl amine, pH 4.5, NaBH3CN 2) CO2 (s)...
Practice Set-lll SET-II 1) C.HNH 1. 2) LIAIH, in ether ? 3) H2O) 1) NaOC Hs ; then CeHsCH CH-Br 2. HCO2C2H5 2) H20 ? & heat H CO2C2H5 3) SOcl, ; then AICI3 & heat 1) Mg in ether 3. ? CHa-CI 2) (CH) CH-CN H2C 3) H3O CH3 1) NaOC,Hs; then CHs-I 2) H3O& heat 4. ? O-CaHs )CHCHO & NaOH; heat SET-III Stage Two Stage Three Stage One Practice Set-lll SET-II 1) C.HNH 1. 2) LIAIH, in...
V. Roadmap problems 1) CH30'Na B H2CrO xs CH3OH A CH3O Na D OH 1) NaOH, H2O E 2) HCl, H20 3) heat Br F H2O, acetone 2) H20, НCI H* Br осн, 1) Сн,оNa" A CH3ONa 1) NaOH, H,О C 2) HCI, НО 3) heat Насо 2) H20, HCI 1) CH3CH2MgBr ether Br EtO Na 1) NaOH, H2O B 2) HC, Hао 3) heat H* C A D OEt E, major product heat 2) H,о" 1) O3 2) (CH3)2S...
1) + NaOH J) OH PCC CH,C1, K) H СН,ОН L) 1. Mg, ether -Br o 2. 3. H,0 M) OH Na Cr 0 H2SO4 4. Propose Mechanism (Show your work) (14 pts) A) CH,CH,CH,OH CHỊCH CHỊCHCHỊCOH
(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*
20) 20) Which of the following syntheses gives 3-methyl-1-hexanol? O Mg 1) A) 2-bromopentane diethyl ether 2) Mg B) 2-bromohexane - diethyl ether 1) HC=0 2) H C) 3-bromopentane Mg diethyl ether 1) CH2CH=0 2) H Mg D) 1-bromobutane diethyl ether 1) CH3CCH; 2) D)D А) А В) В c) C 21) Identify the reagent needed to carry out the following conversion. 21) 0 CHOH CHOH ?, CH CH B) PCC/CH2Cl2 D) K2Cr2O7, H2SO4/H20 A) Os04 C) HIO4
what is reagent 2? A NaOH G Heated KOH Reagent 1 Reagent 2 Product 1 B HgSo. / H2SO4 H Br/ hv с 1.) Na NH2/ heat 2.) H2O LDA OH C1 D Br E к Cl2 Reagent 3 1.) Sia BH home Product 2 CI F NBS/hv 2) HẠO, NaOH
Ter que ethanol/Na/A Nasc NaOE romos 5eq NooH + 5eq Br. mated dilut en KOH, H2O, A Cyclohexanone + N-propyl-1-propanamide then heat the product above + ethanoul bromide then H2SO4
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