Organic Chemistry, Binder Ready Version
Organic Chemistry, Binder Ready Version
2nd Edition
ISBN: 9781118454312
Author: David R. Klein
Publisher: WILEY
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Chapter 27, Problem 39PP
Interpretation Introduction

Interpretation:

Para-methoxystyrene undergoes cationic polymerization more rapidly than styrene need to be explained.

Concept introduction:

Polymerization is a reaction when monomer molecules are reacted to form a polymer chain.  Polymerization can occur via three ways,

  • Cationic polymerization
  • Radical polymerization
  • Anionic polymerization

Cationic polymerization is the polymerization of the monomer (vinyl) with strong electron donating groups.  In this method cationic initiator transfers charge to the monomer which becomes active and further propagates with another molecules.

Anionic polymerization is the polymerization of the monomer (vinyl) with strong electron-withdrawing groups (electronegative groups).  In this polymerization carbanion is the active species.

Radical polymerization is a type of polymerization where the reaction occurs by successive addition of free-radicals.

To explain: To explain why para-methoxystyrene undergoes cationic polymerization rapidly than styrene

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6. Consider the following exothermic reaction below. 2Cu2+(aq) +41 (aq)2Cul(s) + 12(aq) a. If Cul is added, there will be a shift left/shift right/no shift (circle one). b. If Cu2+ is added, there will be a shift left/shift right/no shift (circle one). c. If a solution of AgNO3 is added, there will be a shift left/shift right/no shift (circle one). d. If the solvent hexane (C6H14) is added, there will be a shift left/shift right/no shift (circle one). Hint: one of the reaction species is more soluble in hexane than in water. e. If the reaction is cooled, there will be a shift left/shift right/no shift (circle one). f. Which of the changes above will change the equilibrium constant, K?
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