Frost Circles

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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

chlor-g
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you made this way more simple than my textbook - thank you so much!

yllkavaldez
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This is the first explanation that truly made sense! Thank you, I wish you were my professor.

dylanfrey
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Sir, how can you say that cyclopentadiene is antiaromatic??? It is not planar structure, , hence it should be

debrajmukherjee
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THANK YOU SO MUCH ! It finally clicked after your video <3 excellent explanation.

RachelHannah
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Sir cyclopenradiene is non aromatic but yes it dimerises at room temperature as it's unsatble

asishbauri
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Very nice teaching sir I am kanagaraj from dharapuram. Tamilnadu

dharaitamil
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Lmao that damn windows pop-up. Thanks for the vid

STOPPLSFR
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Thumb up. Great video. Thank you for making this!

PowerPickle
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Cyclopentadiene is non aromatic complete delocalization is not possible there., Please make correction.

manjun
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thank you sooo much for this video!!!!

kayth
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This video is false. the cyclopentadiene is NOT anti aromatic, in fact it’s nonaromatic because it lacks a ring of conjugation due to the sp3 hybridization on carbon 5.

jonathanbarz
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Thank you so much! It was a very clear explanation!

francinysebben