4.1.3 X 10', n = 5:4.3. 4.2. Suggest reasonable mechanisms for each of the following reactions....
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...
please i need a guide on the stepwise mechanisms of the following reactions Scheme 4.2. (Continued) CH, OR 403 CH,OH, DTBP, 25°C C,H,OH, DTBP 40°C НСОН, ОТВР,0°C SECTION 78. n. 58% . 42% in 13% vet. CF.CH OH DTBP. 25°C I-BUOH, 20% H,0,25°C dioxane, 20% H 0,25°C CHCHCH, 49% inv. 6 CHSCHCH 15% inv. K-OCCHg. CH3COH, 50°C Et,NO,CCHE 50% acetone OCCH CH,CHCH 65% Осан, CH CH, * K-OCCH. Cg H₂CC₂Hs OPNB 5+2% inv. CH,CO2H, 23°C C.H.CCHS ACHẠCH 56 15 in....
thanks! On each the following IR spectra, circle and indicate the most important stretching signal from the following choices:N-H, O-H, CEN, CEO, C-O, Top, IR spectrum of Compound 18a: C14H1402 Bottom, IR Spectrum of Compound 18b: C3H120. write your answer on the corresponding square provided (2.5 pts each, 5 pts total) mar 2000 6 C-OR Characteristic IR Stretching Frequencies in cm broad N-H 0-H CEN (3000-3500) (2200-2400) 4000 3000 2000 (1150-1300) 요 RC-O (1600-1750) (1250-1350) (1050-1150) 1500 1000 500 'H-NMR...
Thanks! On each the following IR spectra, circle and indicate the most important stretching signal from the following choices:N-H, O-H, CEN, CEO, C-O, Top, IR spectrum of Compound 18a: C14H1402 Bottom, IR Spectrum of Compound 18b: C3H120. write your answer on the corresponding square provided (2.5 pts each, 5 pts total) mar 2000 6 18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of...