Aromatic, Antiaromatic, or Nonaromatic Practice Session #1

[@aarushpandit8221]

The AMOUNT OF CLARITY is insane!!!!! Thank you so much ❤

[@KWARISIIMAREASPER]

After watching several videos without understanding,a planner compound, you have finally made it for me❤

[@mkhan8902]

Wow after watching a bunch of videos, your video made the most sense. Thank you!!

[@Emilia-we2dc]

wow thank you!! After the whole semester this finally makes sense before my final!!

[@umairshah5697]

Same situation

[@lucastavoulareas963]

Best video on aromaticity. Made me understand it 100%.

[@anushuajana1722]

at 12:23 it will be 3/2

[@josephine4854]

👍🏼

[@5nsport426]

5th compound n = 3/2

[@jasmineramirez615]

highly recommend this video!!! I can do my homework problems now. Thank you

[@NompumeleloKhumalo-d1q]

thank you so much, i understand everything now after watching this

[@noreensyed4877]

You are amazing !!! Final is on monday and you made this 10000 times easier. Thank u

[@cami9295]

Your explanation of the pi bond in the lone pairs 1 C away from a pi orbital just saved my exam grade lol

[@leehailey3479]

Thank you! I was super confused until I watched your videos.

[@inventopotter8582]

I was not able to understand what's the hybridisation of the charged carbon atoms but now I do thanks a lot

[@PSE-i99u]

I can't explain how good your lectures are.❤❤

[@mariatariq5780]

Wonderfully explained! Cleared my concepts about aromaticity👌

[@kevinbenitez7844]

From what I’ve understood, wouldn’t the second to last molecule be non-aromatic since a molecule would rather remain non-aromatic rather than switch to anti-aromatic ?

[@enoughnonymity]

that’s what i think too lol

[@michaeljosechavez]

You are literally one of the best organic chem teachers I've known

[@ChemComplete]

Thank you for the high compliment!

[@chandimchatterjee8444]

Very helpful.... But sir we can also consider that delocalised lone pair are sp2 and localised lone pair sp3 and stays in hybrid orbital... So whenever we see any lone pair participating in resonance we can say it is sp2..

[@bichumonlotha3130]

I find that It's unnecessary to have it subtracted by 2 and find the n value. Simply check if the pi electron value is 4n or 4n+2. If it's the former then it's Antiaromatic, if it's latter then Aromatic. But very very helpful. Thanks!

[@mekdesbelete8766]

very very amazing and clear explanation

[@shrutilipisetha8969]

Thank you so much for complete detailed information

[@PanPan-km5ip]

Big thanks for you, Sir.. Your videos help me a lot, especially for my lecture.. Once again thank you so much. :)

[@ChemComplete]

You are most welcome

[@صديقالشميري-ف6ش]

How know that aromatic is planar?

[@ThaPriusMen]

Great video, thanks a bunch. Quick question. My prof heavily emphasized planarity in his lecture on this topic. Any comments on planarity and it’s importance?

[@ChemComplete]

Hi Dominic, yes planarity is very important and required for aromaticity. The reason planar ring systems are so vital is that they allow for p-orbital overlap which leads to proper conjugation of pi electrons. When a ring fails to meet planar standards, it is classified as non-aromatic (not anti). An example of this is 1,3,5,7-Cyclooctatetraene. One would normally expect anti, but it is non-planar.

[@Hackersuncovered]

thanks so much! Hope you guys are able to push out more Orgo 2 videos haha

[@mizlolia]

Thank youuuuu ❤ I’m finally cleared

[@pasindudeepajith1226]

Great video!! on point❤

[@Alisha-pg9hu]

great explanation !!

[@pragyasingh7591]

thanks a lot for an easy explanation

[@ek3378]

thank you very much it was really helpful and clear

[@latanandb1]

it was really helpful .Keep up ur momentum bro.

[@mattt9868]

Thanks!

[@Czar_Char]

please how do i easily know that a ring structure is going to be conjugated?

[@lizbethjacome3787]

BEST VIDEO !

[@linayasmine9975]

very helpful thank you !

[@suhaibaziz4597]

Thank you

[@AbdulganiyulawalMustapha]

Thanks very u are d best

[@Newsome6277]

goated channel

[@ChemComplete]

Organic is bussin

[@mikaeladeniseresueno4666]

thank you for this!

[@ademmohammed644]

Thanks

[@kennethacheampong7]

Thanks 🎉

[@josephlaguerre5359]

4n+2=8 4n=6 6/4=n n=1.5

[@jadenkinnersley9342]

Makes Sense

[@AK-di4rv]

I find your videos very helpful, but your intro music is very loud and hard on the ears especially with headphones on. Can you please consider changing it for future videos? Thanks for all your effort man!

[@shelbygomez8023]

You are using the same 4n + 2 formula for both aromatic and anti aromatic

[@ChemComplete]

4n +2 = Pi electrons is the formula for determining aromaticity (aromatic or anti)

[@keyannasafforld2341]

thank youuuu so much

[@ChemComplete]

You're welcome!

[@sanahilal6179]

Thank you!

[@andreavacaflor3680]

AMAZING

[@souravkumar2522]

Nice video

[@Briankiptoon.metagulist]

Good am now getting something

[@rassimsimou1594]

Good

[@bekky834]

BLESS

[@souravkumar2522]

In furan how to jutch oxygen is sp2 hybridised ????

[@indrajitnayak2643]

How the nitrogen atom is SP2 hybridized in last compound.

[@mattt9868]

The lone pair is in resonance with the pi bonds. In order to participate in the delocalization of electrons, the nitrogen must keep a p-orbital for overlap purposes and therefore can only be sp2.

[@راقيةباخلاقي-ض5ل]

شكرآ

[@yt_mus1085]

i love u man

[@Lola14826]

Good one

[@saagarsingh7095]

good vid

[@PratikshaMurdeshwar-ik6ht]

4n=6 n=3/2

[@clementgyapong1700]

We need part two on the,same topic with different structures. You are a GOD

[@നിലപാട്-ഷ8ട]

Why pyridine is marked not aromatic???

[@ChemComplete]

Pyridine is aromatic, it was also marked as such in the video!

[@sienamarie8968]

awesome

[@SonFather-x1r]

Best

[@زيدالجبوري-ب2ل]

Value of n in thio pyrane not correct

[@Hornet_Nation]

Math was done wrong at 12:33

[@TogetherinParis]

algebra dude!

[@souravkumar2522]

In last question how nitrogen is sp2 hybridised here ??plz clear confusion

[@mattt9868]

The lone pair is in resonance with the pi bonds. In order to participate in the delocalization of electrons, the nitrogen must keep a p-orbital for overlap purposes and therefore can only be sp2.

[@_krissy_lauren]

you're great

[@rishiruns228]

Thanks for this 🙏

[@ChemComplete]

No problem 👍