Preview
|
Buy lesson
Buy lesson
(only $0.99) |
You Might Also Like
-
Chemistry: Precipitation Reactions -
Chemistry: Electron Shielding -
Chemistry: Second-Order Reactions -
Chemistry: First-Order Reactions -
Chemistry: Acid-Strong Base Reactions -
Chemistry: Organic Polymers -
Chemistry: Rates of Disintegration Reactions -
Chemistry: Reviewing Oxidation-Reduction Reactions -
Chemistry: Elimination Reactions -
Chemistry: Acids and Conjugate Base Reactions -
College Algebra: Solving for x in Log Equations -
College Algebra: Finding Log Function Values -
College Algebra: Exponential to Log Functions -
College Algebra: Using Exponent Properties -
College Algebra: Finding the Inverse of a Function -
College Algebra: Graphing Polynomial Functions -
College Algebra: Polynomial Zeros & Multiplicities -
College Algebra: Piecewise-Defined Functions -
College Algebra: Decoding the Circle Formula -
College Algebra: Rationalizing Denominators
-
Chemistry: Acids and Conjugate Base Reactions -
Chemistry: Elimination Reactions -
Chemistry: Reviewing Oxidation-Reduction Reactions -
Chemistry: Rates of Disintegration Reactions -
Chemistry: Organic Polymers -
Chemistry: Acid-Strong Base Reactions -
Chemistry: First-Order Reactions -
Chemistry: Second-Order Reactions -
Chemistry: Electron Shielding -
Chemistry: Precipitation Reactions
About this Lesson
- Type: Video Tutorial
- Length: 3:11
- Media: Video/mp4
- Use: Watch Online & Download
- Access Period: Unrestricted
- Download: MP4 (iPod compatible)
- Size: 34 MB
- Posted: 07/14/2009
This lesson is part of the following series:
Chemistry: Full Course (303 lessons, $198.00)
Chemistry: Organic Chemistry (8 lessons, $12.87)
Chemistry: Organic Polymers (2 lessons, $2.97)
This lesson was selected from a broader, comprehensive course, Chemistry, taught by Professor Harman, Professor Yee, and Professor Sammakia. This course and others are available from Thinkwell, Inc. The full course can be found at http://www.thinkwell.com/student/product/chemistry. The full course covers atoms, molecules and ions, stoichiometry, reactions in aqueous solutions, gases, thermochemistry, Modern Atomic Theory, electron configurations, periodicity, chemical bonding, molecular geometry, bonding theory, oxidation-reduction reactions, condensed phases, solution properties, kinetics, acids and bases, organic reactions, thermodynamics, nuclear chemistry, metals, nonmetals, biochemistry, organic chemistry, and more.
Dean Harman is a professor of chemistry at the University of Virginia, where he has been honored with several teaching awards. He heads Harman Research Group, which specializes in the novel organic transformations made possible by electron-rich metal centers such as Os(II), RE(I), AND W(0). He holds a Ph.D. from Stanford University.
Gordon Yee is an associate professor of chemistry at Virginia Tech in Blacksburg, VA. He received his Ph.D. from Stanford University and completed postdoctoral work at DuPont. A widely published author, Professor Yee studies molecule-based magnetism.
Tarek Sammakia is a Professor of Chemistry at the University of Colorado at Boulder where he teaches organic chemistry to undergraduate and graduate students. He received his Ph.D. from Yale University and carried out postdoctoral research at Harvard University. He has received several national awards for his work in synthetic and mechanistic organic chemistry.
About this Author
-
- Thinkwell
- 2174 lessons
- Joined:
11/13/2008
Founded in 1997, Thinkwell has succeeded in creating "next-generation" textbooks that help students learn and teachers teach. Capitalizing on the power of new technology, Thinkwell products prepare students more effectively for their coursework than any printed textbook can. Thinkwell has assembled a group of talented industry professionals who have shaped the company into the leading provider of technology-based textbooks. For more information about Thinkwell, please visit www.thinkwell.com or visit Thinkwell's Video Lesson Store at http://thinkwell.mindbites.com/.
Thinkwell lessons feature a star-studded cast of outstanding university professors: Edward Burger (Pre-Algebra through...
More..Recent Reviews
This lesson has not been reviewed.
Please purchase the lesson to review.
This lesson has not been reviewed.
Please purchase the lesson to review.
In this demonstration we are going to make nylon. What we have here are two solutions, one solution is a water solution of 1/6 hexamethylene diamene. This is the molecule that contains amines at the very end of six carbons, one on each carbon.
This is a solution of adipoyl chloride. Adipoyl chloride is a compound that contains two very reactive functionalities called acid chlorides, and they are also at the very end of the molecule. The adipoyl chloride solution is in hexanes. Hexanes is a hydrocarbon and it is lighter than water. What I am going to do, is I am going to pour that hexane solution of adipoyl chloride on top of the water solution and we are going to get two layers, but at the interface of the two layers, what is going to happen is, that the molecules are going to react to form a condensation polymer, and a condensation reaction to form a polymer. The polymer is actually a copolymer, because it consists of two different molecules. The hexane diamene and the adipoyl chloride.
Now the way the reaction works is that because it is copolymer, the end of the hexane diamene molecule reacts with one end of the adipoyl chloride molecule, and then the other end of the adipoyl chloride molecule reacts with another hexane diamene molecule and then the other end of that molecule reacts with the adipoyl chloride and that keeps happening on and on again, until we get this to be a polymer structure. And the key to doing this is the pouring of the two solutions very carefully so that I don't disturb the layers too much, because, like I said, the only place that the reaction can occur, is where the two reactive molecules can actually meet and that is at the interface between the two layers.
Okay, so I am going to pour these now and then I am going to pull out the polymer that is formed in the middle and I am going to roll it around. So now, at the interface you can see, is a molecule of nylon. Now you can tell, this is not exactly the same kind of nylon you get that you make your stockings from. The stocking nylons are made from a similar kind of compound, but they are not exactly made of this composition, and they are made in a much more careful, much more controlled way.
But, you can see that the only place the reaction is occurring is at the interface, and the trick to doing this right is to get it to go right up the middle, if possible. There we go. So as it rolls, you get nylon and the nylon is formed right at the interface between the two layers.
Now of course the thickness of the nylon and all these other properties that you can control are going to be controlled in a complicated process and, in fact, this has been engineered very carefully by the folks that make nylon to optimize this for the right thickness and the right properties that they are looking for in their materials. And over here we are just kind of doing this on the fly. And never the less it illustrates the principle of the synthesis of a copolymer.
And there you have it. I could pull this and dry it and it would be a nice strong string of nylon.
Organic Chemistry
Organic Polymers
CIA Demonstration: The Synthesis of Nylon Page [1 of 1]
Get it Now and Start Learning
Embed this video on your site
Copy and paste the following snippet:
Link to this page
Copy and paste the following snippet:

