It can't and it wouldn't make any difference as only one bond can be formed each side of the triple bond meaning to get stereoisomer you would have to have a carbon after the triple bond with a double bond.
Probably an extension of the fact that electrons in the same orbital must have opposite spins. Check out the Pauli Exclusion Principle if you want to explore further.
This is the third atomic bonding video I've watched, each explaining different things in a very helpful way. Thank you!
Happy to hear that!
thanks for such an easy explanation.This is what I was trying to understand.Now I got it!
So clear and clean. Thank you for actually putting forward the effort to show us - unlike my current professor.
Great Video, helped a lot
Great video. It would be better if you explain in theory on why the pi bond cannot rotate.
Wow better than many professors!! Thank you
omg thank you so much ive been searching everywhere for 24 minutes trying to find the answer and here it is!
I watched many videos and use chat gpt but i cant understant but you explain in the easy explanation thankyou
This man has got an impressive selection of molymods!
Great video and nice basic concepts
Great Video! Can you please make videos on concepts in Analytical and Physical Chemistry?
R R I probably already have. Check out this link to my index bit.ly/2hqSBeD Thanks for the comment by the way
thanks for this great explanation.
This finally makes sense to me, thank you!
🤩
Great video , thank u so much
does the p orbital have space around it for the electron pair because it is the anti bonding molecular orbital or is it not the anti bonding?
great explanation
Thanks ,now i have understood.
Excellent. Really glad to hear it
THAT WAS HELPFUL THANK YOU✨
Thank you so much sir...grateful to you😊
crystal clear thanks alot
Thank u sir .......nice explanation 😄😄
Nice Video Sir...
I got my point by watching your video..
Thank you very much this was so useful.
Yay!
thank you so much helped a lot
can only alkenes form stereoisomers (not alkanes)?
Alkanes can’t because the C-C sigma bond can rotate
is there a reason why there is free rotation in C-C?
Overlap is along the axis of the orbitals
There is deeper theory to this.
the pi bond when rotated cannot get past 90 degrees because it becomes orthogonal, thus it can’t rotate.
It was really good
Thanks - glad you approve :)
why triple bond can rotate freely(as i know they don't have cis-trans isomers)? they have two pi bonds!!!
It can't and it wouldn't make any difference as only one bond can be formed each side of the triple bond meaning to get stereoisomer you would have to have a carbon after the triple bond with a double bond.
@@leo_warren they can
thank u
vry well explained
but y does both the carbon atoms rotate in the opposite direction ?????? plss anyone reply, i wanna know the reason
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Probably an extension of the fact that electrons in the same orbital must have opposite spins. Check out the Pauli Exclusion Principle if you want to explore further.
👍👍
Thank you Sir 🙏
Most welcome
I am student to from now
I never viewed a video like this🙏
Glad you approve!