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- Show Transcribed Text H₂, Pd/C, EtOH MeMgBr (excès) puis H3O+ Me₂CuLi, Et₂O puis H₂O+ Please draw the mechanism step by step ? ? ?2) Formulate the products for all reaction steps of the sequence. Br sformation. Br 1) E107 2) E107 OEt 3) OH" 4) H30* 5) AT irs, andIdentify the reagents necessary for all three methods. ? OH ajay O CH3CH₂ONa ? ? 1) NaOH; 2) CH3CH₂OH CH3CH₂OH, H₂SO4 1) NaOH; 2) CH3CH₂Br OCH3CH₂Br, H₂SO4 □1) SOCI₂; 2) CH3CH₂OH, pyridine OEt
- Draw the missing products and/or reagents in the following multistep synthesis. Select to Draw esc Br ! 1 NaOCH₁, CH₂OH F1 heat @ 2 F2 M 31 #3 Select to Draw F3 040 6 80 $ 4 OH a F4 atv % LO 5 0 F5 Q NAO A 6 c F6 & 7 34790 « F7 A B C E D * 8 B DII F8 1. Hg(OAc)₂, H₂O 2. NaBH4, NaOH RCO₂H 1 OsO4 (catalytic) NMO Bra H₂O 1. BH-THF 2 H₂O₂, NaOH ( 9 CA Done ¯ F9 F10 0 F11 F12Othesis. teps neceossary to synthesize this compound by yl halide; after that you can add any organic or Dound. →1-hexanol )Consider the following compounds: B = HOCH2CH2CH2CH3 CH3 HC C = CH3CH2CH2OCH2CH2CH3 D = a) Which one(s) could be reduced with NaBH4? b) Which one(s) would give a positive Tollens silver mirror test? c) Which one(s) could be oxidized with CrO3? d) Which one(s) would react with 1 or 2 equivalents CH3M9B to make a npound butyl ethyl ether larger alcohol?ph 19. Predict the major organic product that would be prepared from the following reactions through an SN1 mechanism and indicate stereochemistry where appropriate. For each example, draw a complete stepwise mechanism that represents the SN1 mechanism that forms a neutral organic product. Br ed bluodigoplun H₂O OH teal of sidste (1) 10m 2919 01 bazu group and richu Tuoy slab bnc noise Ly? 10 S2 as ograbay of visill storn i wolad uoloss dues erized ban noi3691 dose to tubong ainegi 1091103 ! web en woled solot
- Which is the best reaction sequence to synthesize m-bromobenzenesulfonic acid from benzene? Br ex OH 1) CH3CI, AIC13, 2) Br2, AlBr3 1) ethene, HF, 2) Br2, FeBr3 1) Br2, FeBr3, 2) H2504 1) Br2, FeBr3, 2) CH3COCI, AICI3 1) H2SO4, heat 2) Br2, FeBr3 3 complete total synthesis of Delta9 THC (all the steps of the mechanism)resource from Cengage Learning - Google Chrome ssignment/takeCovalentActivity.do?locator=assignment-take e by the Aldol Condensation (References) OH base + H,0 heat H. H3C H. The aldol reaction is a carbonyl condensation reaction between two carbonyl partners and involves a combination of nucleophilic addition and a-substitution steps. One partner is converted into an enolate ion nucleophile and adds to the electrophilic carbonyl group of the second partner. In the classic aldol reaction, the carbonyl partners are aldehydes or ketones, although aldehydes are more reactive. The product is a B-hydroxy carbonyl compound. In the mixed aldol reaction, the best results are obtained when one of the partners does not have an a-hydrogen. It cannot form an enolate anion and can therefore not undergo self-reaction. The enolizable aldehyde is added slowly to a basic solution of the first aldehyde so that the mixed product is preferentially formed. Under reaction conditions slightly more vigorous…
- Which synthetic route(s) would complete the reaction shown? Br || ||| I and II O I and III ? HO OH + enantiomer Synthesis I: 1. NaCCCH3; 2. Na/NH3(I) ;3. OsO4; 4. NaHSO3, H₂O Synthesis II: 2. NaCCCH3; 2. H2, Lindlar's catalyst; 3. MCPBA; 4. aq. H₂SO4 Synthesis III: 1. NaCCCH3; 2. H₂, Pt; 3. MCPBA; 4. aq. H₂SO4tempt.php?attempt3D1101388&cmid%3D371560 Draw a detailed mechanism showing the formation of all products, be sure to draw all intermediate and show the movement of electros by arrows. F. -Br -OCH3 -OCH3 Heat A - BI aEluestron #5 write out these steps : Friedel-c7ofts acylation, @brominotion, areduction Product storting mo terial