Draw the full arrow-pushing mechanism for the completion steps of the synthesis of Corymine
Draw the full arrow-pushing mechanism for the completion steps of the synthesis of Corymine MeOC CO2Me...
1. Draw a detailed arrow pushing mechanism for the following 2. Provide a reasonable synthesis for the following 1. Draw a detailed arrow pushing mechanism for the following: (6 pts) pTSA + HS SH 2. Provide a reasonable synthesis for the following: (4 pts) or On
What is the full arrow pushing mechanism for the following transformation? Hint: Remember, show all steps to convert the starting material into the product. Do not skip steps for full credit. You have to show how ALL bonds are breaking and forming for this transformation to occur. What is the full arrow pushing mechanism for the following transformation? Hint: Remember, show all steps to convert the starting material into the product. Do not skip steps for full credit. You have...
Draw the full arrow-pushing mechanism for the reaction of t-pentanol with HCl.
1. Draw a detailed arrow pushing mechanism for the following: (5 pts) le mono e com OH + HO 2. Provide a reasonable synthesis for the following: (5 pts)
Draw the mechanism for the hydration reaction including arrow pushing and electrons H PO, HO
Draw the mechanism for the hydration reaction including arrow pushing and electrons H,SO HO
Show FULL arrow pushing mechanism for this reaction, and explain it step by step. Reagent used was c) K2CO3, MeOH, room temp., 1 h (quant.). (please disregard BOTH arrows on s11, as this only one step of a multi-step synthesis) Label all chiral centers on s12 and draw its enantiomer ОН OH C Y і 0 (97 : 3) Л s11 Л s12
Draw the full arrow-pushing mechanism of the reduction of (+)-D-camphor. Briefly address the expected stereochemical outcome of the reaction
3. Draw the arrow-pushing mechanism of the reaction, including all proton transfer steps. 4. Below is the structure of your product, benzocaine, with protons labelled A-E. The 'H NMR spectrum is provided on the next page. Describe the multiplicity (with J values) and integration you would expect to observe for each of the protons. Which peak would you expect to have a higher chemical shift, C or D? Draw resonance OSO structures of benzocaine to explain your reasoning. NH2E
8. (15 pts) Draw a complete arrow pushing mechanism(s) for the reaction below. Please draw every arrow, every bond broken or formed, and the resulting regiochemistry and/or stereochemistry if there is any. 1. N ܂ H I 2. H OH Н. H H