e phone Propose mechanisms for the following reactions t h roug h radi o od osmans...
Meme ylic Acid Derivatives CHO CH,OCC", "(h) O TooCH, - 0 poCH, r the following reactions. CH,OCCI (CH),CHOH - Ph-C-OCH(CH3)2 21-51 P! 0 AH,0 NaOH > Ph-C-0- + CH OH
Mechanisms Propose a mechanism for the following reactions Synthesis Design a synthesis scheme for the following (CH) 110 2) DMS 1) EMBI 2) H0 C, H,0) (C,H,0) AIC, | | |Hºà CH3)2NH (-H,0)
4.2. Suggest reasonable mechanisms for each of the following reactions. The starting materials are racemic, unless otherwise stated. PhCH,CI + POCH3)3 — PhCH POCH3)2 + CH,CI сн. CH3 CH₂ OH BSCI CHA . CH₂ OH pyridine CH1 but e CH₂ CH₂ BSCI pyridine Bs BsO HC=CCH CH CH CI CF3CO H H percevonova co ,C=CCH2CH2CH2O2CF3 n nousemuannen NH2 TOH NaNO2, H20 NO2, H2 C H=0but (CH3), HCIOTY OH NaNO2, H20 NH, HClO (CH3), HOCH=0 Br CH₂ CH₃ CH₃ CH but...
What major Organic product is formed after the following sequence of reactions? 1) NaH, THF 2) Br Br B1 (C) (b) Br Bi a. a Considering both regiochemistry and stereochemistry, what is the major Organic product of the following reaction? о ні. CH-CH, НСІ Снон HC "CH; но CH, НО CH, HCO CH-CH; CH «CH-CH, OCH; CH CH3 ОН нс СІ H; Н;С (6) (c) H.CO CH, Kotic CH.CH НО CH; Но CH.CH Сн, НП). CH,CH; ОН нс Н.С осн;...
Propose mechanisms consistent with the following reactions 8-48 H.SO н.о Br HBr ъ) Он (а) ROOR Br СHBE, Вг Br Вг HЕr (d) NaOH осH CH, Cl Вr НС Br Br CH CH OH Cн CH, Он Н н'. Н,о Он Н "сн CH, CH,CH CH,CH Он н' (g) CH Oн осн, н CH—С-С (h) 2 н Н Н Н Propose mechanisms consistent with the following reactions 8-48 H.SO н.о Br HBr ъ) Он (а) ROOR Br СHBE, Вг Br...
tylphenylmethanol from benzaldehyde (Ph-CHO) (g) cyclopentylphenylm ctan-1-ol from 1-bromohexane (h) octan-1-olf ou would accomplish the following transformations. You may use any additional reagents you ne Show how you would ac A (b) SO3 CH.CH,CH; H OH (racemic) OH O о OH CI_cuci (e) CH, --C-CH2CH2-C-OCH,CH, → CH-CH-CH,CH, ---OCH,CH, O o OH OH ) CH-C-CH.CH-C-OCH,CH, - CH -CH-CH2CH.-CH, Show how you would synthesize the following: Prenylethanol by the addition of formaldehyde to a suitable Grignard reagent D 2-phenylethanol from a suitable...
Draw mechanisms and explain 21.12 Draw the correct structures for the following rxn sequences. 1. OCH CH 2. 1-bromo-propane A 1. OH 2. H+, quench B A, c diethyl malonate B CS HO HOY maller alle and 1. "OCH CH3 1. OH 2. H+, quench ethyl acetoacetate 3. H+, quench B = lors u cha Or OH OH ОН
answer the problem show work thanks CH3 H2O + 1. H-C-CH-CH-CH2 CH3 CH C 2, CHy-CH2-CH-CHOHPCC 25°C 50-55°C + HNO H2SO4 он H2CrO4 CH,CHCH acetone, 35°c Et O 2150113H20 5. CH3(CH2)2MgBr+ CH3(CH2)sC(CH2)sCH3 Nall CH2-CHCH2l H2SO4 140°C 6. CH3CH2CH2OH 7. CHCH CHOH 1) LiAIH(O-t-Bu)3,-78°C 2) H20 8. CH,C-CI HBr 9. CH2 CH-CH-CH2 40°C 10. H3C CIH2 Benzene 100℃ H3C 1. LiAIH/Et2O 11. CH,CH2CH,COH 2. H,0 12. + CH,CH,cCI AIC Benzene, 80°C 13. Br2 heat CH3 AlcI 15. 25°C conc. H2SO4 NaBH4...
g. Ph-C(O)-NH2 4 NaOH Br2 h. (HC)2CH-C(CHa)2 -> HO N(CH3)3 i. Ph-N2, CI- + CuCN --> H30* (cat) Na/ETOH j. cyclohexanone+ H2NOH Pd(OAc)2 (1 mole%) k. Ph-I + 4-O2N-C&H4-HC=CH2 Cul/Pd(PPH3)4) L. HO-CH2-CH2-CC-H +1-CH=CH-(CH2)4-CH3
1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c) ОН ОН (d) Br ОН ОН NH2 2) Draw the condensed and line structures for the following compounds (a) 3,4-dimethylhexanoic acid (b) Phenylacetic acid (c) 3,4-dinitrobenzoic acid (d) 2,2,3-triflurobutanoic acid (e) 3-hydroxybutanoic acid (1) o-hydroxybenzoic acid (g) a-aminopropionic acid 3) Name the following dicarboxylic acids (use both IUPAC and common names) Он (а) НО ОН НО. (b) он ОН ОН (d) ОН он ОН...