30 Annulenes | General Organic Chemistry-1 | JEE Main, IIT Advanced By NS Sir

[@closetoheart6120]

doing regularly .. doing questions from good level books. i am in drop year... thanku sir. intially in class 12 i was hating organic chemistry. but you sir made me love with subject.. thanku so much sir.

[@Itz_shaan]

Bro Aap abhi kaha ho ?

[@vishwajeetchoudhary8264]

What was your result ?

[@chirpchirp8585]

To anyone wondering, why he isn't replying back.. well that's because, notifications hi nhi aati 🤷

[@KavishSethi-qm3iy]

Exactly

[@VladimirPutinIITian]

@@chirpchirp8585 YEAHHHH

[@Saurabh67787]

Thank a lot sir for providing such great lecture

[@MohitTyagi]

Thanks and welcome

[@comedyadda7269]

Mughe nhi lagta kisi ne itna detail me goc padhai hogi Gabbar Singh tutorials sir ne bhi bahot badhiya padhaya ha But you both are best

[@THUNDER-kw3wq]

JEE ADV PLUS ULTIMATE PRO PLUS X lvl sikhaya sir aapne toh. Thank you for providing such awesome quality content for free

[@harshgupta7077]

Konsa iit ma ho aap

[@JEE-.2025]

​@@harshgupta7077tu konse iit me h?

[@PhantomRiderYT]

​@@JEE-.2025tu konse iit me hai??????

[@youthoobuser]

@@PhantomRiderYT tu konse iit me h?

[@shubhampandey3412]

​@@youthoobusertu kon se iit me hai?

[@shresthverma8541]

thank you mohit and neeraj sir for this level contnet...i will surely meet u sir after jee...thank yu for the best JEE content

[@quicksilver90-g8h]

Hua jee?

[@JEE-.2025]

​@@quicksilver90-g8hhua jee?

[@factoboy747]

thank you so much sir , for your hard work, please never stop your work because so many students need you !!!!!!

[@Abhinavmishraone]

Sir 99 % teacher jee advanced ka content nhi da pata Aap to advanced chemistry ka.content da raha hai Love you 💞 sir

[@akshatpandey8300]

No one on KZbin explained resonance and 3d structures... Ns sir supremacy🌞

[@VishalMaurya]

Sir , ye to advance ka bhi advance ho gaya. 😂

[@SONGOKU-tl3ht]

thank you sir for the awesome lectures

[@MohitTyagi]

Most welcome!

[@ShivamKumar-hq3gm]

Kya padhate ho sir ji ❤️❤️❤️

[@asishbauri7433]

Sir u teach very awesome

[@asishbauri7433]

In our coaching annulene 14 is called as weakly aromatic and u took this example this truly shows u are going to cover all the advanced level concepts so no one should ask whether it is of advanced level or not I can assure it's truly Advanced lectures taught from basic

[@MohitTyagi]

Thanks and welcome

[@Chinese...]

Kya squaric acid dianion , squaric acid ka resonating structure hota hai...?? Ya please mujhe squaric acid ke structure bata do koi..

[@akashawasthi3673]

4 resonating structure hote Hai sir ne kisi video mein Bataya h.. in this Playlist only

[@arunabhadhal3662]

Thank you sir

[@MohitTyagi]

Welcome

[@piyushgaming1015]

[8] ANNULENE mein conjugation hi nhi hai as wo non planar hai so why it is called annulene

[@KrishnaHero-rb2km]

Sir I couldn't understand this question 23:00 u have said that neutral resonating structures are more stable than charged resonating structures but here that is different why sir .

[@babygoat-go6jf]

squaric acid will not be polar right...?

[@alphaiitd1]

Thanks sir

[@shreyansh2729]

Sir in eg 29, lecture 13 of GOC -1 when you were comparing stability of resonating structures, then you told there stability of resonating structure with greater no. of covalent bonds is even greater than a resonating structure which was aromatic. And now in examples of polar aromatic compounds you are doing just opposite. Please explain.....

[@yatogami7393]

Lol no , aromaticity is above resonance even in priority order .

[@AAA-ix2hw]

@@yatogami7393 in eg 1 of polar aromatic compounds 1st structure has more pi bonds than second ( both are aromatic) then how the second structure is more stable

[@aditya8778]

@@AAA-ix2hw bro 1st structure is not aromatic the ring is not in complete conjugation

[@aditya8778]

@@AAA-ix2hw and that's why the 2nd structure is more Stable because it's aromatic ,even though the first structure has more pi bonds

[@akshatpandey8300]

Bro don't consider the three pie bonds in alternate fashion as ''aromatic"" The example you r talking abt is the exact resonating structure means the electrons are confined there just like the kekule structures they are not aromatic.. but the hybrid of benzene is...

[@Apoorv-hx4hg]

Don't skip this topic earlier it was not important but now days question are bien framed from this !

[@Ankit_sharma12.]

bhai sir advance level ka pdhate h kya?

[@Ankit_sharma12.]

baise m first time pdhunga to kya m basics samajh pauunga kya?

[@YSo_serious]

​@@Ankit_sharma12.Firstly read ncert than watch lectures from starting

[@Dev-i8r]

FOR MAINS OR ADVANCED

[@prakashsharma4376]

absolutely amazing

[@dr.heinzdoofenshmirtzz]

Isn't O in furan or N in pyrrol is sp3 hybridized then why it's electrons are in sp2 orbital and p orbital? Pls anyone clear my doubt

[@walkingserpent6295]

In furan oxygen has 2 lone pairs, only one pair participates in RESONANCE, hence calculated as 2 pi e-. Other lone pair contributes to determining the orbital of O. So two bonds and one lone pair = 3 , therefore, O is in sp² state.

[@peskyguy157]

One lone pair in unhhybridiazed p orbital perpendicular to plane participates in resonance so planner sp2 O and S atom

[@SLASH.27]

7:30 yeh wala case mere teacher mere ko 10th mein smha rhe the lekin kuch nhi smjh aaya tha lekin ab aa gya

[@asishbauri7433]

Sir will u teach reaction mechanism using some MOT concept of BMO and ABMO and other things

[@kingpatil2882]

Nope

[@laveshgupta6611]

Not in syllabus.

[@ashu-mb2zw]

According to the rules for comparing stability of different resonating structures of the same compound . It was told that no. Of π bonds if to be checked first and layer on aromaticity. Now here its the exact opposite. Why Anyone kindly clear my doubt

[@YSo_serious]

Sir said that π bonds should be checked first But he never said that aromaticity should be checked later If you're comparing 2 compounds then If one is aromatic and other is non aromatic then obviously aromatic would be more stable there is no point of counting pie electrons And if you're comparing 2 aromatic compounds then compare according to that rule

[@suparnagrawal6575]

It is for resonating structure not compounds to find which structure contributes more in a resonance hybrid of compound , aromatic compounds are always more stable than non aromatic and non aromatic than anti aromatic

[@cookiemonster69699]

4:36 8:38

[@Sachin-gh2kn]

Sir in ring strain theory you have told up to 5 member there is high strain means unstable but it is of 10 member it has low ring strain and it should be stable i am asking about 10 annulene(18:05)

[@VishalMaurya]

It is large in shape so it has low repulsion.

[@vikasgiri6458]

bhai there is not much difference in actual angle and ideal angle. second reason is that due to aromaticity it will be highly stable.

[@chandradeep-_-]

If it was to be planar than it would have a high angle strain

[@sanyammishrasm07]

Thank you sir🙏🏻

[@amlesh-kumar45]

How the lone pair of N in pyrol is unhybridised i think it is sp3 hybridised plz clear my doubt

[@saketkumar5457]

Wo lone pair conjugation mein hain and as sir told in Initial lectures of resonance such lone pairs are not counted in hybridization. ( as you can see in the 3d structure they are in same plane with other p orbitals overlapping in same plane => participating in resonance)

[@rishabhpandey216]

Thanks a lot sir

[@pranav3833]

To all students asking iit hua, konse clg mein ho aap, etc etc. Kya hasil ho raha hai tum logo puchke🙁

[@kalimudinansari7993]

bhai teri percentile kitni aayi..?

[@VladimirPutinIITian]

@@kalimudinansari7993 haa batao zara

[@Ashish0]

Konse IIT me h bhai

[@vedantmamidwar4673]

Sir wo carbon ke p-orbital me 1 electron hi kyu hai??

[@fazlurahman8490]

sir you said more multiple bond containing resonating structure are more stable. But in last examples you said aromatic are more stable. is these last examples are exceptions?

[@anonymousyt3547]

nahi aromatic ka characteristic hi wohi hai ki woh sabse jyada stable hai whether another compound is more resonating or not main game starts when we have to compare between two aromatic compounds (according to me)

[@sohamthakkar9080]

If we do ORM 1,2,3,4 ; then is it necessary to do hydrocarbons?

[@capitalistkarl1795]

Haan bro....named reactions hain us mein

[@unstoppablerunner1836]

Lecture 30

[@kaushxl]

3 apr 2023 6:43am

[@parveshprajapati7175]

But pata kaise chalega ki electron p-orbital me hai ya plan k perpendicular??? In pyridine/pirrol???

[@YSo_serious]

Bhai 2 lone pair h Teen p orbital hoti h 2px 2py 2pz Ek orbital mei 2 electron aa skte h Toh 2px mei maan lo hain 2 electrons Toh baaki ke do electrons pz ya py mei rhega Px plane par h toh obviously py perpendicular hoga Structure of atom and chemical bonding ke lecture dekho

[@gavthishivam8980]

Is this advance level contents

[@booksuniversehindi6497]

Yes

[@upendrajod3142]

Bruhh 💀

[@VladimirPutinIITian]

cool

[@saketkumar5457]

Piche ki sari chize hi gayi😅😅ab tak easy lag rha tha

[@nishchaykumar6942]

can anyone pls tell annulenes and uske baad wala portion adv ke liye hai?? time thoda tight hai toh fir i'll cover once exam centric syll ho jaye.

[@adarshsengar2455]

Thanks sir