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Ch. 21 - Carboxylic Acid Derivatives
Wade - Organic Chemistry 9th Edition
Wade9th EditionOrganic ChemistryISBN: 9780135213728Not the one you use?Change textbook
Chapter 21, Problem 63b

The structures of four useful polymers are shown, together with some of their best-known products. In each case,
(i) Determine the kind of polymer (polyamide, polyester, etc.).
(ii) Draw the structures of the monomers that would be released by complete hydrolysis.
(iii) Suggest what monomers or stable derivatives of the monomers might be used to make these polymers.
(b)

Verified step by step guidance
1
Step 1: Analyze the polymer structure provided in the image. The repeating unit contains amide bonds (-CONH-) between segments of the polymer chain, indicating that this is a polyamide. Polyamides are formed through condensation reactions between amines and carboxylic acids.
Step 2: To determine the monomers released by complete hydrolysis, focus on breaking the amide bonds. Hydrolysis of the amide bonds will yield two types of monomers: a diamine and a dicarboxylic acid. Specifically, the hydrolysis will split the polymer at the -CONH- linkages.
Step 3: Draw the structures of the monomers. The diamine monomer will be hexamethylenediamine (H₂N-(CH₂)₆-NH₂), and the dicarboxylic acid monomer will be adipic acid (HOOC-(CH₂)₄-COOH). These are the building blocks released upon hydrolysis.
Step 4: Suggest the monomers or stable derivatives used to synthesize the polymer. The polymer can be synthesized by reacting hexamethylenediamine with adipic acid directly or using stable derivatives such as the diacid chloride of adipic acid (ClOC-(CH₂)₄-COCl) in a condensation polymerization reaction.
Step 5: Relate the polymer to its applications. The polymer shown is nylon-6,6, which is widely used in climbing ropes and violin strings due to its high tensile strength and durability. Understanding the structure-property relationship is key to appreciating its utility.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Types of Polymers

Polymers can be classified into various types based on their chemical structure and the nature of their monomers. Common types include polyamides, which are formed from the reaction of amines and carboxylic acids, and polyesters, which are made from diols and dicarboxylic acids. Understanding these classifications is essential for identifying the type of polymer presented in the question.
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Introduction to Polymers Concept 2

Hydrolysis of Polymers

Hydrolysis is a chemical process that involves the breakdown of polymers into their monomeric units through the addition of water. In the context of the question, complete hydrolysis of the polyamide structure will yield the corresponding amine and carboxylic acid monomers. This concept is crucial for determining the monomers released during hydrolysis.
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Introduction to Polymers Example 2

Monomer Structure and Derivatives

Monomers are the basic building blocks of polymers, and their structures dictate the properties of the resulting polymer. In addition to the original monomers, stable derivatives can also be used to synthesize polymers. Identifying these monomers and their derivatives is key to understanding how the polymers in the question can be synthesized and what alternatives exist for their production.
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Related Practice
Textbook Question

Macrolide antibiotics, including erythromycin and azithromycin (Zithromax®), contain a large ring lactone. One of the largest ever reported is Gargantulide A, the structure of which was determined by the research group of Prof. William Gerwick of the Scripps Institution of Oceanography (Organic Letters, 2015, 17, 1377–1380). Isolated from a Streptomyces bacterium, it kills pathogenic bacteria like MRSA and Clostridium difficile, but it proved too toxic to the test animals to continue further testing.

(a) Identify the lactone that makes this a macrolide structure.

(b) How many rings does this structure contain? How many atoms are in the largest ring?

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Textbook Question

The structures of four useful polymers are shown, together with some of their best-known products. In each case,

(i) Determine the kind of polymer (polyamide, polyester, etc.).

(ii) Draw the structures of the monomers that would be released by complete hydrolysis.

(iii) Suggest what monomers or stable derivatives of the monomers might be used to make these polymers.

(a)

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Textbook Question

The structures of four useful polymers are shown, together with some of their best-known products. In each case,

(i) determine the kind of polymer (polyamide, polyester, etc.).

(c)

(d)

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Textbook Question

In Section 21-16, we saw that Sevin insecticide is made by the reaction of 1-naphthol with methyl isocyanate. A Union Carbide plant in Bhopal, India, once used this process to make Sevin for use as an agricultural insecticide. On December 3,1984, either by accident or by sabotage, a valve was opened that admitted water to a large tank of methyl isocyanate. The pressure and temperature within the tank rose dramatically, and pressure-relief valves opened to keep the tank from bursting. A large quantity of methyl isocyanate rushed out through the pressure-relief valves, and the vapors flowed with the breeze into populated areas, killing about 2500 people and injuring many more.

(a) Write an equation for the reaction that took place in the tank. Explain why the pressure and temperature rose dramatically.

(b) Propose a mechanism for the reaction you wrote in part (a).

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Textbook Question

An unknown compound gives a mass spectrum with a weak molecular ion at m/z 113 and a prominent ion at m/z 68. Its NMR and IR spectra are shown here. Determine the structure, and show how it is consistent with the observed absorptions. Propose a favorable fragmentation to explain the prominent MS peak at m/z 68.

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Textbook Question

Explain this curious result. What does this reaction tell you about the relative reactivity of esters and ketones?

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