4.5 Nylon 10,6 is made using adipic acid and decamethylene diamine. It's full name is poly(iminoadipoyliminodecamethylene), thus calling nylons by numbers is much easier. A. What is the repeat structure of nylon 10,6? B. If decamethylene diamine is reacted instead with isophthalic acid, a different nylon is made. Draw this new repeat structure. C. One of these two polymers is opaque and one is transparent. Which one would you expect to be opaque? Which transparent? Explain why. (Use the internet to look up chemical structures of the monomers; hint for part c: look up the difference between ortho, meta and para bonding in phenyl groups)

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter16: Aldehydes And Ketones
Section: Chapter Questions
Problem 16.71P
icon
Related questions
icon
Concept explainers
Question
4.5 Nylon 10,6 is made using adipic acid and decamethylene diamine. It's full name is
poly(iminoadipoyliminodecamethylene), thus calling nylons by numbers is much easier.
A. What is the repeat structure of nylon 10,6?
B. If decamethylene diamine is reacted instead with isophthalic acid, a different nylon is made. Draw this
new repeat structure.
C. One of these two polymers is opaque and one is transparent. Which one would you expect to be
opaque? Which transparent? Explain why.
(Use the internet to look up chemical structures of the monomers; hint for part c: look up the difference between
ortho, meta and para bonding in phenyl groups)
Transcribed Image Text:4.5 Nylon 10,6 is made using adipic acid and decamethylene diamine. It's full name is poly(iminoadipoyliminodecamethylene), thus calling nylons by numbers is much easier. A. What is the repeat structure of nylon 10,6? B. If decamethylene diamine is reacted instead with isophthalic acid, a different nylon is made. Draw this new repeat structure. C. One of these two polymers is opaque and one is transparent. Which one would you expect to be opaque? Which transparent? Explain why. (Use the internet to look up chemical structures of the monomers; hint for part c: look up the difference between ortho, meta and para bonding in phenyl groups)
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 4 steps with 4 images

Blurred answer
Knowledge Booster
Nomenclature of Organic Compounds
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9781305580350
Author:
William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:
Cengage Learning
Chemistry: An Atoms First Approach
Chemistry: An Atoms First Approach
Chemistry
ISBN:
9781305079243
Author:
Steven S. Zumdahl, Susan A. Zumdahl
Publisher:
Cengage Learning
Macroscale and Microscale Organic Experiments
Macroscale and Microscale Organic Experiments
Chemistry
ISBN:
9781305577190
Author:
Kenneth L. Williamson, Katherine M. Masters
Publisher:
Brooks Cole
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9781305080485
Author:
John E. McMurry
Publisher:
Cengage Learning
Introductory Chemistry For Today
Introductory Chemistry For Today
Chemistry
ISBN:
9781285644561
Author:
Seager
Publisher:
Cengage