4. Show the mechanism for the following transformation. As always, be sure to show all intermediates and curved arrows. (Hint: The first step involves two copies of the ester.) a) NaOMe OMe OMe b) BzBr H,SO4. OMeHཉྫO ་།། Ph Ph H3O+ heat Η Ph
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- The answer choices for part b ["How would you convert the alkene to a epoxide?"] are: (a) Br2/NaNH2 in liq NH3; (b) mCPBA; (c) OsO4Thank you!Show how to accomplish the following alkylation. (a) Step 1 (i) Specify the reagent used in this step. (ii) Draw the structure of the intermediate formed in this step, compound A. (B) draw the structure of the reagent needed for this step. (C) specify the reagent used in step b C Show how to accomplish the following alkylation. [References] Step 1 Step 2 compound A Step 3 CO₂Et (a) Step 1 (i) Specify the reagent used in this step. (ii) Draw the structure of the intermediate formed in this step, compound A. 12) Complete the mechanisms for the following reactions. A) = H₂0 H₂ soa B) OH H₂SO4 Hint: Consider the methyl Shift mechanism. What if you did a similar Shift with the quatrinary carbon?
- Propose a mechanism for this isomerization.Select the major product from the reaction sequence shown. 1) MezNH, [TSOH], - H2O 2) 3) HO مال منه NMez .OH ? ka ta(ORGANIC CHEMISTRY) (mechanisms) please give a answer for the following mechanism. Provide a detailed stepwise mechanism for the following transformation.
- Alcohols react with sulfonyl chlorides to form sulfonate esters. Only the O-H bond of the alcohol is broken in the reaction, and so no inversion of configuration occurs. The resulting sulfonate esters are reactive in SN1 and SN2 reactions since the sulfonate group is a very weak base and is therefore a good leaving group.Draw curved arrows to show the movement of electrons in this step of the mechanism.Alcohols react with sulfonyl chlorides to form sulfonate esters. Only the O-H bond of the alcohol is broken in the reaction, and so no inversion of configuration occurs. The resulting sulfonate esters are reactive in SN1 and SN2 reactions since the sulfonate group is a very weak base and is therefore a good leaving group.Draw curved arrows to show the movement of electrons in this step of the mechanism.Show a stepwise mechanism by pushing arrows and drawing all intermediates. Draw a detailed mechanism for the addition of H2O to 2-methyl-2-pentene in the presence of H2SO4.
- Provide a stepwise mechanism to explain the formation of the products in the following reaction. Remember to show electron flow using the appropriate type of arrows please!!!! (draw it out) You do not need to include a termination step.Come up with a synthetic route to achieve the following transformation.Chemistry please answer both in detail as im confused. thank you! Write the necessary steps to perform the following transformation. (Hint: This is a two-step procedure, H₂C For the reaction in problem 5, draw a stepwise mechanism for the first reaction