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Pentadiene is nonaromatic because of the SP^3 hybridized carbon, you should include a (+) if you want to say it's antiaromatic
Yes. Pentadiene is nonaromatic due to non conjugates system is created here due to sp3 carbon
Thanks, I was thinking the same thing, but I'm just in ochem 3 so I wasn't confident in that
Sir,how can you say that cyclopentadiene is antiaromatic??? It is not planar structure,,hence it should be nonaromatic!!!!!
oh dear - yes, you are absolutely right. Even if you discount the lack of planarity, it's not completely conjugated either, so of course it must be nonaromatic. That is my mistake - not sure what I was thinking when I said that. My apologies
you made this way more simple than my textbook - thank you so much!
This is the first explanation that truly made sense! Thank you, I wish you were my professor.
Thanks Dylan, glad it was helpful; this concept really isn't that complex, but at first glance it can be really daunting.
THANK YOU SO MUCH ! It finally clicked after your video
Wonderful, thank you so much!
Sir cyclopenradiene is non aromatic but yes it dimerises at room temperature as it's unsatble
Thumb up. Great video. Thank you for making this!
Lmao that damn windows pop-up. Thanks for the vid
Thanks for the video, Sir.
So helpful!!
Thank you!
great video!!
thank you sooo much for this video!!!!
Cyclopentadiene is non aromatic complete delocalization is not possible there., Please make correction.
Thank you so much! It was a very clear explanation!
I wasted 30 seconds of my life on ads
i love u man
Thank you sir
Thank you
Can you do this for polycyclic compounds?
Pentadiene is nonaromatic because of the SP^3 hybridized carbon, you should include a (+) if you want to say it's antiaromatic
Yes. Pentadiene is nonaromatic due to non conjugates system is created here due to sp3 carbon
Thanks, I was thinking the same thing, but I'm just in ochem 3 so I wasn't confident in that
Sir,how can you say that cyclopentadiene is antiaromatic??? It is not planar structure,,hence it should be nonaromatic!!!!!
oh dear - yes, you are absolutely right. Even if you discount the lack of planarity, it's not completely conjugated either, so of course it must be nonaromatic. That is my mistake - not sure what I was thinking when I said that. My apologies
you made this way more simple than my textbook - thank you so much!
This is the first explanation that truly made sense! Thank you, I wish you were my professor.
Thanks Dylan, glad it was helpful; this concept really isn't that complex, but at first glance it can be really daunting.
THANK YOU SO MUCH ! It finally clicked after your video
Wonderful, thank you so much!
Sir cyclopenradiene is non aromatic but yes it dimerises at room temperature as it's unsatble
Thumb up. Great video. Thank you for making this!
Lmao that damn windows pop-up. Thanks for the vid
Thanks for the video, Sir.
So helpful!!
Thank you!
great video!!
thank you sooo much for this video!!!!
Cyclopentadiene is non aromatic complete delocalization is not possible there., Please make correction.
Thank you so much! It was a very clear explanation!
I wasted 30 seconds of my life on ads
i love u man
Thank you sir
Thank you
Can you do this for polycyclic compounds?