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- Draw the starting structure that would lead to this polymer under radical conditions. Drawing A or Av AIBN (radical initiator) tt. CI oProvide the missing starting materials, reagents or produtsIntermidiates and reagents of the following two final products from a Acetylene Note: the final products are different reactions but use the same starting material.
- Which reagent(s) adds HBr to a double bond in a non-Markovnikov fashion via a radical mechanism? A. Br2 B. Br2, hv or light C. HBr D. HBr with CH3OOCH3Draw the starting structure that would lead to this polymer under radical conditions. Select to Draw A or Av AIBN (radical initiator) CH3 ofIf the reaction shown below obeys Markovnikov’s rule, which labeled carbon gets the H?
- 3D Draw the starting structure that would lead to this polymer under radical conditions. Drawing A or Av AIBN (radical initiator) tfQuestion 8: Draw the products formed when each diene is treated with 03 followed by CH3SCH3? a. b. C. d. Question 9: Draw the products formed when each alkyne is treated with 03 followed by H₂O.Draw the electron-pushing mechanism for the propagation steps of the allylic bromination reactions below. You may omit NBS in your mechanism, and use Br and Br2.