awesome explaination sir. sir last year few questions in chemistry jee mains was totallly unexpected can u give us the list of such short areas for which we did not prepare well
sir u said that the lone pair won't be donated as the ring becomes non aromatic but we can see that even by donating the pi electrons it forms a 3 membered ring and also the ring has lost its aromaticity. So the reason for which we didn't want the lone pair to be donated, eventually that had only happened even after dealing with the pi bond
They are acidic because after removing H , the minus charge is very well stabilised by resonance with double bonds and the ring is eventually becoming aromatic. So they are acidic. Hope it clears!
Sir now i am in 10 after 10 i m deciding to join sri chaitanya to prepare for iit jee.sir pls guide me whether my decision is right or shud i try some other coaching. Sir only u can help .sir pls reply
Sir, do pathway me apne pehla Wala naa hone ka reason aromaticity loose bola aur baad me jo dusra pathway banaya usme bhi aromaticity loose ho Raha hai + vo unstable 3member ring bhi ban rahi hai to sir phir dono pathway galat ho ja rahe hai .. to ye reaction kaise possible ho rahi hai
sir u said that the lone pair won't be donated as the ring becomes non aromatic but we can see that even by donating the pi electrons it forms a 3 membered ring and also the ring has lost its aromaticity. So the reason for which we didn't want the lone pair to be donated, eventually that had only happened even after dealing with the pi bond
Another good one!Please cover such type of different or exceptional cases of organic chemistry.Very helpful for advanced
How's life
Sir please upload Beckmann Rearrangement :)
Explained in detail....awesome
awesome explaination sir. sir last year few questions in chemistry jee mains was totallly unexpected can u give us the list of such short areas for which we did not prepare well
u are doing a great job sir............
Sir last eg mein sirf do pi bonds hi bane so who benzene ring kaise bana
thanks sir
Really well explained . Thank you sir!
Thanks a lot sir.
Sir where can I find more problems based on abnormal reimer tiemann reaction ?
dear sir, at 5:37, why t-Butoxide abstract hydrogen from that carbon ??? kindly reply sir.
because its acidic hydrogen
this helped in solving a particular MS chouhan question
thanks vineet sir.
Most welcome, Check out our channel and app, There are many more relevant lectures for your target year.🤗
Sir kaise differentiate kare ki kab RTR hoga aur kaise Abnormal RTR hoga. Please clarify...
Cyclopetadiene is the differentiator
Most helpful video ..sir ...hatsoff to the efforts ...thanku
Most welcome
Sir please don't mind apka first attempt me jee main kya rank tha?? Kyunki maine bhi is bar drop kiya h iit krn k liye.......
thank you so much sir you helped alot me in understanding this reaction I WAS GETTING CONFUSED WITH IT BUT NOW EVERYTHING IS CLEAR
On point!
another awesome video
sir u said that the lone pair won't be donated as the ring becomes non aromatic but we can see that even by donating the pi electrons it forms a 3 membered ring and also the ring has lost its aromaticity. So the reason for which we didn't want the lone pair to be donated, eventually that had only happened even after dealing with the pi bond
sir pleasr reply
thank you sir! super helpful :)
what is effect of - I group on phenol in reimer teman reaction and why....
Activating grp due to +M
Thnx a lot sir
very nice..
nice sir
At 1:16 you said that these H atoms are acidic bt did not explain why? Pls help!
because ring is becoming aromatic after their loss :)
Yup
They are acidic because after removing H , the minus charge is very well stabilised by resonance with double bonds and the ring is eventually becoming aromatic. So they are acidic. Hope it clears!
jaise do carbonyl ke bich me jo h hota h wo acidic hota he waise
uske bad resonance energy bad jaeygi
Sir how aldehyde group is being also produced as a product in this reaction???
Please explain!!!
How to identify whether the reaction is abnormal or not
with the normal rtr reaction there is always some chance abnormal rtr
6:52
Sir you r the most helpful person. In my life..👌👌👌
U teach really very good questions with beautiful explanation really fab work pls bring more videos in the same way n TQ so much
400k subs congrats
He is awesome!
Sir now i am in 10 after 10 i m deciding to join sri chaitanya to prepare for iit jee.sir pls guide me whether my decision is right or shud i try some other coaching. Sir only u can help .sir pls reply
aamir rizwan kha se ho?
Jyothi Swaroop M. mumbai
aamir rizwan there are better than sri chaitanya, pls consider
For example
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nice and very good concept
gr8 video ...
Sir, between Cl and F why is Cl removed and not Cl?
Cl is better leaving group
Sir, do pathway me apne pehla Wala naa hone ka reason aromaticity loose bola aur baad me jo dusra pathway banaya usme bhi aromaticity loose ho Raha hai + vo unstable 3member ring bhi ban rahi hai to sir phir dono pathway galat ho ja rahe hai .. to ye reaction kaise possible ho rahi hai
Same doubt😓...bhaiya do you know the reason now??
Awesome
nice
Thanks,keep watching & shower your love & support for more such lectures .🤞
always
carbene must be singlet.
sir u said that the lone pair won't be donated as the ring becomes non aromatic but we can see that even by donating the pi electrons it forms a 3 membered ring and also the ring has lost its aromaticity. So the reason for which we didn't want the lone pair to be donated, eventually that had only happened even after dealing with the pi bond
nice and very good concept