Draw the missing organic structures in the following multistep synthesis. Show all structures at physiological pH (pH = 7.4). Ignore any inorganic byproducts formed. H2 N. Select to Draw CF3CO2H CH2Cl2 Q I BnOH Select to Draw I H2SO4 I H2O I он- I > BOC-Ala DCC Select to Draw I I I
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- ↓ Draw the missing products or reagents in the following multistep synthesis. Ignore any inorganic byproducts. app.101edu.co I Select to Draw 3 equivalents NaNHa heat Q Cl2 (1 equiv) hv 1 equivalent Cl2 Select to Draw (CH3)3COK heat Select to DrawPh, S- H,O Ph. R. 'N 'N' H. The final step in the Edman degradation is the acid-catalyzed rearrengement of the ATZ derivative to the PTH derivative. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions Ph Ph 0-H :A N- H-A Hö --R -R H. H.Please don't provide handwritten solution...
- 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. H₂SO4Synthesis of Nefidipine from benzaldehyde and alkene derivative . Preferably use structures1