We have seen two methods for converting a carboxylic acid and an amine into an am- ide. Suppose that you start instead with a dicarboxylic acid such as hexanedioic acid and a diamine such as 1,6-hexanediamine. Show how amide formation in this case can lead to a polymer (a macromolecule of molecular weight several thousands times that of the starting materials). HO H,N. NH, Nylon 66 + HO Hexanedioic acid 1,6-Hexanediamine (Adipic acid) (Hexamethylenediamine) the material produced in this reaction is the high- molecular-weight poiymer nylon 66, so named because it is synthesized from two 6-carbon starting materials.

We have seen two methods for converting a carboxylic acid and an amine into an am- ide. Suppose that you start instead with a dicarboxylic acid such as hexanedioic acid and a diamine such as 1,6-hexanediamine. Show how amide formation in this case can lead to a polymer (a macromolecule of molecular weight several thousands times that of the starting materials). HO H,N. NH, Nylon 66 + HO Hexanedioic acid 1,6-Hexanediamine (Adipic acid) (Hexamethylenediamine) the material produced in this reaction is the high- molecular-weight poiymer nylon 66, so named because it is synthesized from two 6-carbon starting materials.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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