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428,950 Views • Jan 29, 2007 • Click to toggle off description
Views : 428,950
Genre: Howto & Style
Date of upload: Jan 29, 2007 ^^
Rating : 4.852 (72/1,877 LTDR)
RYD date created : 2022-01-22T02:09:33.248779Z
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YouTube Comments - 112 Comments
Top Comments of this video!! :3
So that's how Spider-Man held all that webbing
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YES!! That's 3 minutes of my 10 minute presentation on Nylon done!
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man i was there 3 years ago when this was recorded. man that was a fun class
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Interesting! They way he explained it was engaging. Dude surely knows how to keep his students interested.
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My chemistry 30 teacher sent me here since we're in our organic chemistry unit. What a joy to watch!
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The cpmpound is easily hydrolyzed (reacted with water) or oxidized. If it is not fresh, no reaction happens because there is no sebacoyl chloride.
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This really brought back fond memories of High School chemistry. My teacher at the Bronx High School of Science(Class of '74) was Mrs. Frank and I remember sitting mesmerized by this demonstration.
That doesn't explain why I went on to major in Electrical Engineering....
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i loved this class. Was always fun going too.
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in germany i normally hate chemistry and physics..but this is some kind of special^^
i love these vids!
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why isnt he wearing safety goggles
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This may sound like a silly question, however I am attempting to recreate this experiment without making too much or too little nylon. Approximately how much of each liquid did you use?
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Thanks a lot for this video but I have a question. Is the synthetic nylon the same in composition to commercially made ones. If not, what test can I use to different them.
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is it strong?
And How can i spin this???
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thanks for sharing this, way cool
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It's amazing 👏
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Is it a real nylon? Does it have the strength of a nylon rope? I just wanted to know because I did not do the experiment you did.
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@sakuranohana1523 The organic solvent is n-hexane. A straight chain, not a cyclic molecule.
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what were the 2 chemicals he used? and can you make any other fiberous materials like this?
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@endospores Actually, he didn't use sebacoyl chloride in this reaction. Besides, it can't form an aqueous solution because it actually reacts with water. He said he used a di-acid, either adipic acid or sebacic acid.
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@nicolhaidi
10 years ago
that dude knows how to keep the students focused
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