Polypropylene is used in making polymer banknotes and textiles.

  1. Give the structure of polypropylene.
  2. Is this an addition polymer or a condensation polymer?
  3. What conditions (cationic, anionic, free-radical) would be the most appropriate for polymerization of propylene? Explain your answer.

Short Answer

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(b) Polypropylene is an addition polymer since, no molecule is lost in the formation of polypropylene.

(c) Cationic polymerization would be the most appropriate for polymerization of propylene.

Step by step solution

01

Step-1. Explanation of part (a):

Polypropylene is formed from propylene monomer, and it is a type of polyolefin which is harder than polyethylene. It has low density and high heat resistance. It is a tough, rigid, and crystalline thermoplastic produced from propylene monomer. It is second most widely produced volume plastic after polyethylene.

Structure of polypropylene

02

Step-2. Explanation of part (b):

Addition polymers are produced from addition polymerization and no by-products are formed in the process. Molecular weight of the resulting polymer is an integral multiple of monomer’s molecular weight. Reaction results in high molecular weight polymers at once. Polypropylene is an addition polymer since during the polymerization process, no molecule is lost.

03

Step-3. Explanation of part (c):

Cationic polymerization would be most appropriate for the polymerization of propylene. During the polymerization process, tertiary carbocation forms which is stable and is the driving force for the mechanism and thus, cationic polymerization is the pathway which is followed. Propylene is a monomer in this mechanism and adds onto the growing chain of polymer to generate polypropylene. No molecule is lost in this mechanism and high molecular weight polymer results.

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Most popular questions from this chapter

Plywood and particle board are often glued with cheap, waterproof urea-formaldehyde resins. Two to three moles of formaldehyde are mixed with one mole of urea and a little ammonia as a basic catalyst. The reaction is allowed to proceed until the mixture becomes syrupy, and then it is applied to the wood surface. The wood surfaces are held together under heat and pressure, while polymerization continues and cross-linking takes place. Propose a mechanism for the base-catalyzed condensation of urea with formaldehyde to give a linear polymer, and then show how further condensation leads to cross-linking. (Hint: The carbonyl group lends acidity to the N - Hprotons of urea. A first condensation with formaldehyde leads to an imine, which is weakly electrophilic and reacts with another deprotonated urea.)

. Poly (trimethylene carbamate) is used in high-quality synthetic leather. It has the structure shown.

(a) What type of polymer is poly (trimethylene carbamate)?

(b) Is this a chain-growth polymer or a step-growth polymer?

(c) Draw the products that would be formed if the polymer were completely hydrolyzed under acidic or basic conditions.

Chain branching is not as common with anionic polymerization as it is with free-radical polymerization and cationic polymerization.

  1. Propose a mechanism for chain branching in the polymerization of acrylonitrile.
  2. Compare the relative stabilities of the intermediates in this mechanism with those you drew for chain branching in the cationic polymerization of styrene (Problem 26-6). Explain why chain branching is less common in this anionic polymerization.
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