There was a guy that was convicted of fraud for claiming his fuel reformer design used a mechanism that looked like this, to take hydrogen from water vapor, under high heat, and catalyze fuel vapors with the hydrogen that gets exchanged with metal in the pathway to the intake. Does that concept actually have merit, or was he taking part of this real chemistry and just using it to confuse people into thinking something impossible? Granted, a lot of his demonstrations were really cheeky, and would also lead people to believe he was trying to sell another "runs on water" scam, but if temperatures around that of 4-stroke engine exhaust can cause hydrogen to leave water and get stuck to a metal catalyst, it would seem like he was at least partially vindicated, if not wrong by not really grasping the entirety of the system and misapplying it.
In terms of the actual electro interactions between the double bonded carbons and hydrogens, do the two carbons Turn into radicals and that’s why the hydrogens interact with them?
What about when you have more than one double bond such as cyclohexatriene? how does the stereo-chemistry work for that? can't find an answer anywhere and I know my professor will be inclined to ask XD
Because the alkene coordinates (aligns) with the surface of the metal meaning there is only one side where the Hydrogens (on the metal) will interact with the alkene's double bond.
Final Exams and Video Playlists: www.video-tutor.net/
bruh my professor is awful at explaining things and watching your videos has helped me out so much
For anyone so inclined, the mechanism part starts at 8:58 or so.
Thanks
Thank you!!
ua-cam.com/video/6iw8mC51vqY/v-deo.html
Thank you!
@@sarfarazchempreparation4580 uyasphaphela
Chemistry was never like this ... without you
"chemically speaking" whenever I hear your voice...I know I'm saved
I feel that we're destined to be together.😵💫 chemistry is veeryy ez with your explanation 🥰 I got an "A" in my first test thanks to u❤️
the fact that this man has taught me chemistry 1-3 and organic chemistry is fucking beyond me. My professors are quite useless at this point.
He helped me in some advanced inorganic and biochem as well
You are my hero!
I was wondering how hydrogen atoms are absorbed on metal surfaces?
thank you thank you thank you. I need to get in the habit of watching these videos more during my courses cause they help so much !
Your always there for me.....😊 I love you bro. Keep it up👌🏼
Indian cold fusion "experts" could use this video lol. Great video comment to feed the alg
What does that mean?
@@kumarvikramaditya9636 it's been 2 months I don't remember nor do I care to rewatch the video to gain the context I'd need
There was a guy that was convicted of fraud for claiming his fuel reformer design used a mechanism that looked like this, to take hydrogen from water vapor, under high heat, and catalyze fuel vapors with the hydrogen that gets exchanged with metal in the pathway to the intake. Does that concept actually have merit, or was he taking part of this real chemistry and just using it to confuse people into thinking something impossible? Granted, a lot of his demonstrations were really cheeky, and would also lead people to believe he was trying to sell another "runs on water" scam, but if temperatures around that of 4-stroke engine exhaust can cause hydrogen to leave water and get stuck to a metal catalyst, it would seem like he was at least partially vindicated, if not wrong by not really grasping the entirety of the system and misapplying it.
Helpful video! Your voice is so relaxing 👌
Thank you so much (Sun 20 Dec 2020, 4:07 AM)
Is it protic or aprotic? Because I forget.
If our production isn't stereospecific, how can our product be pure?
@@mynamejeff124turtle2come on help me out…PROFESSOR
Is it Breaking Bad reference as Walter were rosting Victor?
@@LiubomyrLynyshyn yes!
How Ni /Pt / Pd work as catalyst!?? Can you please explain mechanism behind this !?!
It is very simple
@@abdulsalamkhuhro9637 than explain it ...
But I have no any channel sorry.
It’s all MO theory
In terms of the actual electro interactions between the double bonded carbons and hydrogens, do the two carbons Turn into radicals and that’s why the hydrogens interact with them?
You are my hero! Thank you so much!
Great video
Thank you!! So in hydrogenation we only get syn product??
Yes
Thank you so much, my problems are solved
I love your videos thank you so much!
What about when you have more than one double bond such as cyclohexatriene? how does the stereo-chemistry work for that? can't find an answer anywhere and I know my professor will be inclined to ask XD
It's probably too late now, but cyclohexatriene is actually benzene and will usually not hydrogenate unless under extreme conditions.
Your brilliant 💗
it was helpful really.....
thanks man!really really thanks!
1:36 cycloalkene -> cycloalkane
6:24
Sir please discribe how its hybridisation change from sp2 to sp3
You're amazing
Bro your the best
Thankyou for your efforts sir🙏🙏
Thank you sir
In cylcoalkene ozonolysis takes place ?how can we say that in this compound ozonolysis will not take place but hydrogenation will occur ?
Why is it always a Syn addition?
Because the alkene coordinates (aligns) with the surface of the metal meaning there is only one side where the Hydrogens (on the metal) will interact with the alkene's double bond.
ua-cam.com/video/FPh-G9wb1HA/v-deo.html watch this
Rate depends on
Thanx bud!
:)
wtf no mecanism
language please hindi
Learn English first
@@renuagarwal15 no need to be so rude