Added: 5 years ago
From: robertburkottawa
Views: 113,462
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  • Oooo D:

  • ...is he a wizard?

  • amazing !

  • Putrescine is diaminobutane, Bobby, not diaminopropane.

  • only if classes in my highschool were like this

  • Where's the SAFETY GLASSES???!!!!!!!

  • wow tat's really long nylon!!!!..

  • Do you make sutures and fishing line out of that??

  • The guy looks like bill Murray

  • He mentioned that a group of people are in the Guinness Book for making the longest thread of nylon. I can't find any info on this. Would anybody care to direct me to where I can find out more?

  • what would happen, if you put the liqids in a bottle and shake it?

  • @XTwina Since the reaction takes place at the border of the two liquids, agitation will cause the solution to react in the entire volume. The result is a mass of nylon that looks not unlike a phlegm ball from an elephant.

  • YES!! That's 3 minutes of my 10 minute presentation on Nylon done!

  • pulling the nylon out look like pulling the noodle out XD

  • real good man.

  • what were the 2 chemicals he used? and can you make any other fiberous materials like this?

  • man i was there 3 years ago when this was recorded. man that was a fun class

  • @atsusamuno your a piece of shit.

  • hey dude you cant get any u know y because u have a baby penis and i hope it falls off and satan eats for a snack

  • @sabram24 Man...!

  • Yes I know

  • Question!, how come my nylon came out like a big chunk of a solid

  • If you have the mixture of the diamine and dicarbonyl and just stir it up, they will just react all together, not at a nice thin layer like here

  • well, did you see how he poured the hexane diamine onto the side of the beaker? that caused the two substances to only touch in a small area. if there was a larger area, possibly pouring straight into the first chemical, rather than a tilted beaker, or if there was agitation, or stirring, then you would end up with a "glob" like product

  • we did this in high school

  • lol what h.s? this is orgo

  • palatine high school illinois

  • n C4H8(COOH)2 + n C6H12(NH2)2 --> Nylon + 2n H2O

  • how do you know that... *-*

  • @Jakub0071 at the end it's (2n-1) H2O since you have a string, not a whole ring

  • I understand the theory behind hexanediamine and decandiachloride and that it reacts in the boundary between Water and Hexan - but why does it have to be aquious Sodiumhydroxide and not just water?

  • It could be that the aqueous solution of sodium hydroxide acts as a catalyst for the reaction, while water might not have the same effect

  • the diamine is basic and will pick up protons for water with its lone pair, making the lone pair on the nitrogen less reactive

  • Thank you.

  • now why can my prof do cool stuff like that?

  • i loved this class. Was always fun going too.

  • Wow, that was interesting!

  • what solutions are needed?

  • we saw this experiment today in class.

  • are you an organic chemist

  • cool my biologie teacher did that experiment in class today lol very nice.

  • asking question .. so the hexamethylenediamine is in the cyclohexane solvent and the sebacoyl chloride is in the Aqueous Sodium Carbonate?

  • @sakuranohana1523 The organic solvent is n-hexane. A straight chain, not a cyclic molecule.

  • sweet... all those organic chem classes and i know what he's talking about...

  • Funny

  • Bob ... why did'nt you post these videos back in 2005-2006, I cud've done much better:(

  • 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....

  • we can do better, because we are chemical brothers XD

  • awesome reaction. looks like a big loogi!!

  • i counted 22 meters before he gave up

  • I got to do this in my organic chemistry lab

  • in germany i normally hate chemistry and physics..but this is some kind of special^^

    i love these vids!

  • If the sebacoyl chloride is not fresh the string will break easily right?

  • The cpmpound is easily hydrolyzed (reacted with water) or oxidized. If it is not fresh, no reaction happens because there is no sebacoyl chloride.

  • @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.

  • Guitar strings.

  • what is the use of nylon thease days

  • these are great . thanx

  • The mushroom cloud thing scared the living s### out of me when I was six, Now it is just a bad memory.

    Difunctional amide?

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