
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Transcribed Image Text:5. Write a curved arrow mechanism for the anionic polymerization
of the epoxide below.
요
NaOCH3
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- 2. Provide the product, arrow-pushing mechanism (only one) and polymer notation for the following polymerization. 304-00-- H₂N- -NH₂ DMFarrow_forward國 小 山 C A app.101edu.co YouTube Maps e ELEAD Login O AIMS :: Login O VINpoin Gmail sdp. -> Draw the starting structure that would lead to this polymer under radical conditions. Drawing A or Av AIBN (radical initiator)arrow_forward62. What starting material will generate the indicated product with the given reaction sequence? 1. NaOEt in ethanol 2. Do 3. H₂0, H₂O, heat (A) (C) ? Im ů OH HO 63. What is the (A) OEt (C) OH monomeric unit for this polyhydroxyalkanoate (PHA) biodegradable polyester? HO (B) OH CI HO OH Eto 0= (D) Eto O HOT OEt المهام الله (D) (B) HO OEt O OH you OH Parrow_forward
- 1. Use curved arrows to show the initiation and propagation steps in the radical addition of HBr to 2- methylpropene in the presence of peroxides. 2. Draw a mechanism for the formation of polystyrene in the presence of peroxides. (Show the chain initiation and at least 2 rounds of chain propagation.) styrene monomerarrow_forwardClass Ratieypation Q3. Draw polymer for med by polymeriz zation of anionic lots ofarrow_forwardD?arrow_forward
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