Chapter 26: Q7P (page 1328)
Draw the important resonance forms of the stabilized anion formed in the anionic polymerization of methyl acrylate.
Chapter 26: Q7P (page 1328)
Draw the important resonance forms of the stabilized anion formed in the anionic polymerization of methyl acrylate.
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Get started for free. (a) Draw the structure of gutta-percha, a natural rubber with all its double bonds in the trans configuration.
(b) Suggest why gutta-percha is not very elastic, even after it is vulcanized.
Compare the molecular structures of cotton and polypropylene, the two major components of thermal underwear. One of these gets wet easily and holds the water in contact with the skin. The other one does not get wet, but wicks the water away from the skin and feels relatively dry to the touch. Explain the difference in how these two fabrics respond to moisture.
(a) Nomex®, a strong fire-resistant fabric, is a polyamide made from meta-phthalic acid and meta-diaminobenzene. Draw the structure of Nomex.
(b) Kevlar®, made from terephthalic acid (para-phthalic acid) and para-diaminobenzene, is used in making tire cord and bulletproof vests. Draw the structure of Kevlar.
The mechanism given for cationic polymerization of isobutylene (Mechanism 26-2) shows that all the monomer molecules add with the same orientation, giving a polymer with methyl groups on alternate carbon atoms of the chain. Explain why no isobutylene molecules add with the opposite orientation.
Propose a mechanism for the reaction of phenyl isocyanate with methanol.
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