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- Draw the organic product formed in the following reaction. H-N Job OEt OEt [1] NaOEt [2] CI [3] H₂O+, A NHAC HO "CH₂ edit structure ...The given reaction scheme is an example of which type of reaction? O || R₁-C-OH + R₂-OH Oxidation Fischer esterification Nucleophilic substitution Reduction Rearrangement reaction Acid O || R₁-C-O-R₂ Meeting in "General"(h) CHCO CI CH3CO2H, 50 °C Draw the major product(s) of the reaction.
- Q, - write a Mechanism that explains hint he stereochemisty (sed pmacal rearangemendy a) CotH6 fonn Hcl b) HeoH O wr,te he Mechanism fer OH CHBrg NAOH (Carbene)(j) Br HO- 25°C Draw the major product(s) of the reaction. Include all stereoisomers formed as part of the major product.4) For the following reaction map, provide the products, or reagents/ direction of the reaction arrow! MeO OMe MeO OH
- 3) Please draw the structures that correspond to omitted structure for each of the following synthetic sequences. HO Cro3 Cro3 (a) Product `OH Product H,0 HO PCC Cl РСС (b) Product (e) Product OH HO РСС NABHA (f) Starting Material (c) Product OH ELOHWhat is a major product of the sequence of reactions shown in the box? A) Br 이 ? Pd-cat, Base heat B) D)Identify the major product of the following reaction sequence. 1) [H*], H₂NNH2, (-H₂O) 2) KOH/H₂O, heat HO₂C HO₂C HO CO,H OH OH There is no reaction under these conditions or the correct product is not listed here.
- 5. Draw the major and minor products of the following reaction. (H3C),CCH,CH3 H2SO4 heat онWhich 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. H₂SO44) Draw the complete electron-pushing arrow mechanism for the following reductions. Explain, using resonance contributors, the regiochemistry that results in each case. ỌMe Na, MeOH ? NH3 CHO Na, MeOH ? NH3