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- a) Provide the complete mechanism for the following reaction. Meo CH;CH2NH2 CH;OH b) Design a synthesis for this primary amine starting from benzene. CH2CH,NH2 HO(d) Complete the following reaction (with mechanism) : Ph Ph + MeNH, NaBH4 EtOH, A ? 3Draw 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 ...
- Show Transcribed Text H₂, Pd/C, EtOH MeMgBr (excès) puis H3O+ Me₂CuLi, Et₂O puis H₂O+ Please draw the mechanism step by step ? ? ?Show a possible mechanism for the following reaction 1) EtMgBr (еxcess) 2) H20 Et OH Me •Me "Et w..Show the organic product formed when 4-methylpentanal is heated with sodium methoxide in methanol as solvent. Show the steps in the mechanism as reactant is converted to final product. show appropriate arrow pushing and any charges,and draw a box around the final product.
- * Your answer is incorrect. Which synthetic route(s) would complete the reaction shown? Br ? 1 SO II O III O I and II Oland III OH + enantiomer HO Synthesis I: 1. NaCCCH3; 2. Na/NH3(1):3. OsO4; 4. NaHSO₂, 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. H₂SO49. Draw the structure of product, substrate or condition in the following reactions (should clearly show the stereochemistry). Ме 12, KI, NaHCO3 OH a) Ме C3H13021 Ме BH3 "Me b) then H2O2, NaOH OH Ме Br2, H20 c)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 ELOH
- Monensin (1) is a potent antibiotic. JACS 1980, 102, 2118-2120. 1. Use arrows provided a pathway from (1) to (2) when we add a mild base sodium bicarbonate followed by iodine (I2). 2. What was a similar reaction between Br2 and an alkene? What did we name the intermediate?2. Show the organic product formed when methyl propanoate is reacted with lithium diisopropyl amide, then methyl ethanoate is slowly added to the mixture. The mixture is neutralized with aqueous acid to obtain a neutral product. (A) Show the steps in the mechanism as reactant is converted to final product. show appropriate arrow pushing and any charges. (B) Draw a box around the final product.Q17. Compound 1 can undergo an intramolecular reaction to give cyclic product 2. Using curly arrows, show the mechanism of this reaction – note that the mechanism involves more than one elemental step - and draw the structure of 2; chemical formula is provided as guidance. H,N. CsHgNO + CH;OH 2