Write the steps and reagent required to perform the following synthetic transformation 3. Page | 9...
all part of one question please answer neatly, Part B Write the steps and reagents required to perform the following synthetic transformation. You may need more than one step. Page 17 CH2-B1 + H₂N Protein CPMV chanism for the hydrolysis of the ester below in basic solution Pag КОН CH
4. pushing mechanism for the following synthetic transformation and write in the product. You Write an arrow should show relative stereochemistry in your intermediate steps. (20 pts) Br2 CH3 + enantiomer Et Syn or Anti addition? Syn or Ant Gircle: E or Z Write mechanism below:
What is the best choice of reagent(s) to perform the following transformation? * Could possible explain step by step * Thanks in advance 1. What is the best choice of reagent(s) to perform the following transformation? Br OH OH
Question 3 4 pts Provide the correct order of synthetic steps for the following transformation: Step 1 HE [ Choose] Step 2 [ Choose) Step 3 [Choose] Step 4 [ Choose] Step 5 [ Choose]
What reagent(s) would be required to accomplish the transformation shown? Please show all steps. What reagent(s) would be required to accomplish the transformation shown? HA 60 SES -các-CH, C-CHE O 1 . H2, PL H2, Lindlar's catalyst Na, liq. NH3, then H20
Provide a 6 step synthetic route for the following transformation. 6 Steps OEt
Write out the retrosynthesis, forward synthetic steps, reactants, and intermediates for the following synthetic scheme. Then pick one forward synthetic step and draw the mechanism associated with that step. 1. OH Write out the retrosynthesis, forward synthetic steps, reactants, and intermediates for the following synthetic scheme. 2. CH2CH3 Write out the retrosynthesis, forward synthetic steps, reactants, and intermediates for the following synthetic scheme. Then pick one forward synthetic step and draw the mechanism associated with that step. 1. OH Write...
Write out the retrosynthesis, forward synthetic steps, reactants, and intermediates for the following synthetic scheme. CH2CH3 O Write out the retrosynthesis, forward synthetic steps, reactants, and intermediates for the following synthetic scheme. CH2CH3 O
2 S 3 % 5 tab w page 9 7. How would you perform the following chemical transformation? OH
Propose synthetic routes (a series of reactions; not a mechanism) for the following transformations. Transformation (a) can be done in 2 steps. Transformation (b) can be done in 4 steps.