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Polyaramid is a term applied to polyamides containing aromatic groups. These polymers were originally made for use as tire cords but have since found many other uses.

  1. Kevlar is used in bulletproof vests and many high strength composites. The structure of Kevlar is


Which monomers are used to make Kevlar?

b. Nomex is a polyamide used in fire-resistant clothing. It is a copolymer of:

Draw the structure of nomex polymers How do the structures of Kevlar and Nomex differ?

Short Answer

Expert verified
  1. The monomers used to make kevlar are 1,4-benzene-dicarboxylic acid and 1,4-diaminobenzene
  2. Kevlar is a para-aramid while Nomex is a meta-aramid

Step by step solution

01

To find Which monomers are used to make Kevlar

First, to be able to identify the monomers that make up Kevlar, we must observe its overall structure and pinpoint which monomers are used in its structure.

Observe the C=O bonds and N-H bonds that are present in kevlar; these are from the monomers used which are 1,4-benzene-dicarboxylic acid and 1,4-diaminobenzene.

Hence The monomers used to make kevlar are 1,4-benzene-dicarboxylic acid and 1,4-diaminobenzene

02

Monomers are used to make Kevlar

The difference between Kevlar and Nomex lies in their structure, Kevlar is a para-aramid while Nomex is a meta aramid

Hence Kevlar is a para-aramid while Nomex is a meta-aramid

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Most popular questions from this chapter

Answer the following questions regarding the formation of polymers.

a. What structural features must be present in a monomer in order to form a homopolymer polyester?

b. What structural features must be present in the monomers in order to form a copolymer polyamide? (Hint: Nylon is an example of a polyamide. When the monomers link together to form nylon, an amide functional group results from each linkage.)

c. What structural features must be present in a monomer that can form both an additional polymer and a condensation polymer?

In 1994 chemists at Texas A\&M University reported the synthesis of a non-naturally occurring amino acid:

a. To which naturally occurring amino acid is this compound most similar?

b. A tetrapeptide, phe-met-arg-phe-is synthesized in the brains of rats addicted to morphine and heroin. (Theindicates that the peptide ends ininstead of.) The TAMU

scientists synthesized a similar tetrapeptide, with the synthetic amino acid above replacing one of the original amino acids. Draw a structure for the tetrapeptide containing the synthetic amino acid.

c. Indicate the chiral carbon atoms in the synthetic amino acid.

d. Draw the geometric isomers for this synthetic amino acid. (Hint: Refer to Exercise 25.)

Why are cyclopropane and cyclobutene so reactive?

Draw a structural formula for each of the following.

a. 3-methylpentanoic acid

b. ethyl methanoate

c. methyl benzoate

d. 3-chloro-2,4-dimethylhexanoic acid

Why is it preferable to produce chloroethane by the reaction of HCl(g) with ethene than by the reaction of Cl2(g) with ethane?

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