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- Reagent 3 list; commas separate the choices benzylamine,cyclohexlbromide, cyclohexylamine NaBH3CN catalytic H+, h30, NaOH Reagent 4 list; CH3(Ch2)2MgBr, cyclohexylamine NaBH3CN catalytic H+, Na2 Cr2 O7 H2O H2SO4,cyclohexabromide reagent 5 list; cyclohexylamine NaBH3CN catalytic H+,CH3(Ch2)2MgBr, cyclohexabromide, benzylamine6. Complete reaction scheme below indicating reagents, catalysts and conditions, and side product trigil bezinslog si6101fon 290b 1l (b Senines levirba 6 gaubong nasamots gniwollot ads to doinW 01 sniowl (6 CH3 40 CH3 Scansgowi (d Ege nodie) ( nsgyxo (b NO₂ 19m02 2i gniwollet sits to mainW II HOowing reactions proceeds via an SN1 or SN2 of the reaction: (b) S2 pro85 39 Br tort atubong auonsV HMPAnoitutitadua
- itagram video by Mrbioo N X D Time-ManiMo 2019 X E New ta Content Owt21Oine teaching and te O https://cvg.cengagenow.com/ilr/takeAssignment/takeCovalentActivity.dolocatorasigrment-take Draw the structure(s) of the major organic producti(s) of the following reaction. NH2 Trace of acetic acid ethanol • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right comer. Separate multiple products using the + sign from the drop-down menu. C P opy aateWhat is the best description of the product distribution from the reaction shown (- OTF=triflate, trifluoromethanesulfonate) Na OH,coo CH, COOHH,0 C D. DA mixture of compounds B and D OA mixture of compounds A and C OA mixture of compounds A and B OA mixture of compounds A and DAs far back as the 16th century, South American Incas chewed the leaves of the coca bush, Erythroxylon coca, to combat fatigue. Chemical studies of Erythroxylon coca by Friedrich Wöhler in 1862 resulted in the discovery of cocaine, C17H21NO4, as the active component. Basic hydrolysis of cocaine leads to methanol, benzoic acid, and another compound called ecgonine, C9H15NO3. Oxidation of ecgonine with CrO3 yields a keto acid that readily loses CO2 on heating, giving tropinone. (a) What is a likely structure for the keto acid? (b) What is a likely structure for ecgonine, neglecting stereochemistry? (c) What is a likely structure for cocaine, neglecting stereochemistry?
- Electrostatic potential maps of anisole and thioanisole are shown. Which do you think is the stronger acid, p-methoxybenzoic acid or p-(methylthio)benzoic acid? Explain.Draw the predicted major products of the following reactions. Ph OHC., (PhP);RhCI PHCN, A H,CCH, Grubbs I, CH,OCl, Rh(CO),CI CO R-0 B(OH)2 Pd(OAc)2 K3PO4 Pd(OAc)2 K3PO4Provide the major organic product of the reaction shown. NV L Draw the molecule on the canyas by choosing buttons from the Tools (for bonds), t [1] A OH 4' 1. NaH эсе 2. CH₂CH₂CH₂CH₂I H: 120 EXP. CONT L Marvin JS ? ** I U ZOS CI Br
- pt pt pt 1 pt C|Chec C Chee C I need 8 https://east.cengagenow.com/ilrn/takeAssignment/take CovalentActivity.do?locator-assignment-take b Answe F3 • You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. [References] Draw the structure of the one tertiary (30) alcohol with the molecular formula C5H120. Submit Answer F4 90-85 4+ F5 ¤- CHA 95 IF6 C Draw *+ a O. IF F7 C/C MOTION EYE C Draw F8 SONY Draw F9 C Home WEB k ak DISPLAY F10 F11 C-Draw C One Touch Web Access WithcThe following reaction should under go a(n) H₂C SN1 Br NaSPh DMF A/ reaction.NaOMe MeOH A B D E F What are the two starting materials? of