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)

Chemistry: Principles and Practice
3rd Edition
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Chapter22: Organic Chemistry And Biochemistry
Section: Chapter Questions
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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)
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