19) write a detailed stepwise "electron push" reaction mechanism for the S1 reaction. You do not...
7. MECHANISM Using electron push arrows, provide a logical, detailed, stepwise mechanism for the following transformation. Be sure to show each step in the mechanism, including initiation, and propagation steps as well as at least one termination step. HBr → Br ROOR
Write the complete stepwise mechanism for the following reaction Show all intermediate structures and all electron flow with arrows. Draw the mechanism for the following reaction. Show stereochemistry for every step of the reaction.
b. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and include all intermediate structures OH HCl OCHz + CH3OH - 4,0
20. Write a detailed, stepwise mechanism for the following free-radical monobromination reaction. + Brz
8. Write a complete, stepwise reaction mechanism for the reaction shown. Indicate a electron flow with arrows and draw all intermediato structures (12 points) CH3OH (excess) HCI, heat OCH OCHa
predict the product for the following reaction and draw the
detailed stepwise mechanism for the following formation of the
product showing all intermediates at each step.
Br 1) xs NaNH2 2) H20
predict the product for the following reaction and draw the
detailed stepwise mechanism for the following formation of the
product showing all intermediates at each step.
Br 1) xs NaNH2 2) H20
Hydration of alkenes under aqueous acidic conditions. Draw the detailed stepwise mechanism for this reaction. Be sure to show all steps, intermediates, formal charges, and show the movement of electrons with curved arrows. You do not need to draw transition states. H2SO4 H20 ?? The hydration of alkynes can also occur under aqueous acidic conditions however, instead of forming the alcohol, a ketone is formed. Draw the detailed stepwise mechanism for the conversion of the alkyne to the ketone (one...
5. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate structures. (10 Points) CH3 Br2 -Br (or Cl2) "H| Br
Write a detailed mechanism for the reaction above, then draw curved arrows to detect electron reorganization for the step below. To make a bond to a specific carbon of a double bond, use the "hit box" nearest that carbon.