Trick to Compare any Free radical stability | IIT JEE & NEET | Vineet Khatri Sir | ATP STAR Kota

[@theflea2539]

I didn't studied goc in class 11th. Now whenever my teacher teaches something of class 11th related i just come here and clarify my all doubts. thank you sir . Agar IIT pahucha to aapko bhi equal share doonga baki teachers jitna .

[@atpstarkota]

Glad, There are many more lectures for your target year, so check out our channel and app.💯

[@prettypikachoo7633]

Pahucha kya bhai iit me

[@HarshitSingh-oh8gx]

@@prettypikachoo7633 sayad pahuch gya hoga

[@HarshitSingh-oh8gx]

@@prettypikachoo7633 bhai tu NEET ya JEE kiska aspirant hai

[@jethalalgada5359]

​@@HarshitSingh-oh8gx ha abhi tak to pahuch jana chahiye . bada admi ho gya humko bhul gya hoga shayad.. Koi na

[@rishimasinha3303]

Thank you sir for providing short and crisp videos in shortest time possible💕💕

[@akashkushwaha836]

Best teacher hai Atp me

[@shadabmalik5466]

Ally free radicle is more stable than benzyl due to loss of aromaticity

[@mental_block]

sir Aap great ho plz chemistry ki videos upload karte rahiye.I'm really dependent on you

[@sheshayiroy7386]

Made my confusions clear, A good one.

[@Deepanshu-qv8kg]

Kadak..........km time m topic clear ho gya 😅😅

[@JanardansinghYadav-nw9cx]

One of the best channel on youtube to clarify the concepts .

[@sanskarpatil574]

Thank you sir this videos are really helpful for me in lockdown 2020

[@AjayYadav-ds3wz]

Thanks you sir. We will need a teachers like you .

[@vinesbybharatyadav1789]

Best video lectures i ever seen

[@krishvika17]

Thank you sir 😊

[@NityanandMaurya-or2jj]

Thanks you sir ❤ AAP jitne smart dikhate ho utane hi smart padhate bhi ho ❤❤❤❤

[@dhruvbhargava5651]

Even a 3⁰ free radical is more stable than benzyl free radical! Also in the resonating structures of benzyl free radical there is disturbance in aromaticity that's why it is less stable as compared to allyl free radical!

[@mohamedjaasim8211]

In one word u r a legend

[@vaibhavjaiswal471]

Suppose there is an electron withdrawing group auch as CN attached to C atom with free radical. Will this be more stable by resonance than 6 alpha H carbon free radical?

[@atpstarkota]

Yes,you are talking about recent JEE Main Question 😊

[@vaibhavjaiswal471]

@@atpstarkota Thank you so much sir for such a swift reply☺️

[@bkshouharda6952]

Sir thermochemical calculations and data show that allylic radical is more stable than benzyllic radical by 2 kJ/mol.

[@asharanipippal2757]

Brahmakumar Shouharda Ghosh I will clear ur confusion , Benzylic radical is more stable than allylic . But on the basis of bond dissociation enthalpy allylic radical is more stable.

[@prathamsunkad9409]

sir can we say there is equal resonance in C so thats why it should be most stable 3:53

[@harshvardhan3907]

Thanks a lot

[@wow.organic]

@atpstarkota Allyl radical is more stable than benzyl radical. You taught wrong that benzyl radical is more stable than allyl radical .

[@AnishkaBansal-m8l]

Yes you are true

[@poojakumari9334]

Sir you can't explain the stability order between 3 degree free radical and benzyl free radical...??

[@vrunn]

F Cl Br I radicald mein kiski stability zyada hogi?

[@_baffledbrain_0454]

Ty so much sir ....really thankful😊😊😊🙏

[@SahilKumarSah12]

Thanks sir u are magical .....so easy ..

[@Divyanshi-jiit]

Does mesomeric effect also contribute to free radical stability

[@kushshah007]

thank you so much sir... The biggest deal of your videos that makes better than others is that it is short and quick point to point and with more examples....

[@whyp5445]

These videos clear misconceptions to a large extent

[@neelamdhaniya5651]

very thankful vedio sir

[@adityaagrawal5407]

Dhanyawaad

[@janardan976]

Its very helpful and easily understandable

[@yatinnargotra2834]

greatly explained in a good speed thank u sir

[@rajarshibose5122]

this things are not written in many books so we usually confuse to understand mechanism properly

[@shivamagarwal2715]

there is 1 alpha hydrogen in c also, why hasn't that been considered wouldn't that make c more stable than b

[@diptanilroy5021]

No because resonance effect is more dominating than hyperconjugation

[@danishpk1803]

Sir you are genius

[@kumudpanchal5619]

Nicely explained

[@toukirjn555]

Keep it up sir....we are always with u

[@sheemasiddiqui9927]

great video thank you so much !

[@AnamikaPrajin]

Sir at 3:00 , There is no substituent or functional group attach to the ring then how does Inductive effect affect the third structure?

[@hikikomorir420]

Anamika Prajin the adjacent carbon to the radical in the ring would also provide inductive effect

[@mdrehanfazal8462]

thank you sir.

[@joydeepdas8018]

Bt sir does radical show inductive effect

[@karansingh-fd4ym]

what if a group such as F or O is attached the the benzene ring (the benzene ring is connected to a methyl free radical)? will we consider only inductive effect of the F or O or will we consider mesomeric effect too?

[@Sheetal-bn1td]

Sir 8th jan shift 1, question on free radical is quite confusing , they have reacted the primary free radical alkyl, not secondary free radicals,, according to NTA answer key, sir I'm very confused in this question, I'll be thankful if u cleared my doubt

[@mayaagarwal317]

Awesome!!!!!

[@RakeshMishra-lq2kk]

U are doing b tech in Bangalore, aren't you???

[@ppdudes6175]

Sir what is carbene and nitrene

[@rajarshibose5122]

free radical oxygen and carbon - which species is more unstable

[@kumudlikhar9554]

Well explained

[@furqanhaider2430]

Secondary free radical ma ksa inductive effects produced ho giya ... inductive effects to upto 3 carbon wla compund ma hota h n?? Plz sirconfrm me

[@Troughcrest6932]

well explained👍

[@RishabhJain-ip1vr]

Does -m stabilise radical

[@akshaysanthosh799]

thku sir its very helpful

[@rajarshibose5122]

so it is the reason of kolbe electrolysis first step

[@shivajideshmukh8931]

sir in 2nd last example how hyperconjunction occurs ?

[@nandinig7585]

Is stability of free radical and carbocation done in the same way?

[@mrkeshri4786]

Yes

[@rajarshibose5122]

which is right

[@gigachadkartik]

Sir, can we conclude that being electron deficient it will act as Carbo cation?

[@vanshamiit]

pata hai 6 saal late hu, but no we cannot do that

[@rajarshibose5122]

I am confused because the step of that reaction can happen due to the fact co2 is stable leaving group or free radical stability

[@ramniwasprajapat3382]

Thanx sir

[@manvendrasinghsingh9923]

thanks

[@rajarshibose5122]

sir thanks

[@rajarshibose5122]

the step in which o. becomes R.

[@sagarenterprise6970]

ty

[@sitikanthabaliarsingh8177]

@2:51 i don,t think there is any resonance in the second case , as there is no conjugation

[@jeeasprint8254]

Kahi bhi kuch bhi lag jata h kuch samajh nhi aa rha hai

[@mindyourbusiness46]

Sir, can you clear this doubt of mine. Which is more stable? 1) C6H5CH2ČH2 2) CH3CH2ČH2 Sir, Č refers to the Carbon with the electron.

[@AbhinavJha-s4b]

Seedhi baat no bakwas

[@rajarshibose5122]

because of electronegativity

[@rajarshibose5122]

but how.two facts are different

[@rajarshibose5122]

this things are not written in many books

[@thetrigger8086]

Roses are red Violets are blue The title is in English The video should be too

[@shivampawar4450]

ARE YOU BLIND ITS CLEARLY WRITTEN....""IN HINDI""

[@yourlordandsaviouryeesusbe2998]

You moron.