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)
Classes Of Functional Groups
Organic Chemistry deals mostly with carbon and hydrogens, also called hydrocarbons, but those groups which replace hydrogen and bonds with carbon to give a characteristic nature, unique of their own, to the hydrocarbon they are attached to, are called functional groups. All the compounds belonging to a functional group undergo reactions in a similar pattern and are known to have similar physical and chemical properties.
Characteristics Of Functional Groups
In organic chemistry, we encounter a number of special substituent groups which are attached to the hydrocarbon backbone. These groups impart certain characteristics to the molecule of which it is a part of and thus, become the highlight of that particular molecule.
IUPAC Nomenclature
In Chemistry, IUPAC stands for International Union of Pure and Applied Chemistry which suggested a systematic naming approach for the organic and inorganic compounds, as in the beginning stage of nomenclature one single chemical compound was named in many ways by which lead to confusion. The need for this approach aroused as the number of chemical compounds newly discovered were increasing (approximately 32 million compounds) and the basic concept of nomenclature i.e. the trivial nomenclature and the derived system of nomenclature failed to overcome the challenge. It is an important task to name a chemical compound systematically and unambiguously which reduces lots of confusion about the newly reported compounds.
![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)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F8431a8c5-6804-4c93-872c-b668a4efa765%2F125d8487-a4a8-4a83-8faa-cef2e6eb1a79%2F7bt13so_processed.jpeg&w=3840&q=75)
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