@@sachinranaiitb sir cld u plz upload a video on youtube of the imp ques to be done from the cengage books and what's the right way to read them. hope u won't disappoint us.
#respect...when other iitbombay guys are busy doing their own study and trying to make a good engineer......u r helping create lakhs of excellent engineers.
Shreyasi : Can u plz provide family wise compilation of reactions for P block? I would be really relieved....U inspire me everyday Bhaiya... Thank u so much :-)))
sir in the first que when we get nucleophiic benzene ring, why will it attack O2? doesnt O2 have free electrons around it..thus nucleophile would not prefer to attack it right?
Bhaiya in the video at time 8:52 you R doing pinnacole pinnacolon ,so according to migratory aptitude instead of methyde shift there should be hydride shift
Sir how does Grinard Reagent chooses between C=O and same come compound containing O as hetero atom ?which place will it attack.. I mean which bond is weaker?
videos bahut helpful h. :) continue making the same. if possible pls make a video on coordination compound,thermodynamics and probability before 10th may !
bhaiya pls try and upload a video on biomol.and polymers before Jee advanced 2017 as these two topics are very crucial wrt jee and it would be of a great help. . .and Bhaiya ur way of teaching chem is just fabulous . thanks a lotfor all these beautiful video s.....
Sir, I have been watching all your chemistry and maths videos .It would be a big help if you could explain physics also (EMI, fluid mechanics, modern physics,wave optics) The way you explain is just amazing. Thanks again
Sir at 15:33. H30+ is 2nd reagent right.So why are You taking it before the complete reaction of LiAlH4.i.e First the Compound should be attacked with 4 H- and Only then H3O+ should be considered right?.Please Clarify this.
He used the h+as the catalyst as we know every catalyst has to be removed after occurrence of any organic reaction he did me shift to remove h from oh attached to the carbon. If he didn't shifted the methyl and removed h+ from the adgecent carbon he will get an unstable reaction intermidiate.hope you found it useful
Very good video, keep it up. Could you suggest me more UA-cam channels like yours. Preparing for Jee mains through self study. Need to follow good channels like yours in
the way u represent these reaction ,,,,I swear no one can represent I ve seen u r the best bro. please what u think important about thermodynamics please upload
Dear sir..will you please provide videos on physics ,chemistry specified to state public service commissions...the questions that were asked in the particular examination is very static and factual..almost 80 percent.
Too late to answer but just for the sake of other people, the methyl shift takes place as carbcation is stable on the 1st carbon and then plus charge shifts to adjacent carbon and simultaneously O donates its lone pair, and then h+ gets removed. He shortened the mechanism just for sake of simplicity.
Sir lone pair of chlorine is in resonance with benzene so how can we use mg in presence of ether as u told that it is weak and it will not form grignard reagent
sir at 7:46 (approx ) in the example which you were discussing , there is an alcohol already formed . alcohol's hydrogen is acidic . will the second mole of grignard reagent choose to abtract the acidic hydrogen ?
sir cld u plz upload a video on youtube of the imp ques to be done from the cengage books and what's the right way to read them. hope u won't disappoint us.
sir but while shifting takes place methanide shift is lot slower than hydride shift due to the bulky nature of methyl group and moreover if you shift the hydrogen you get a even more stable carbocation with three extra hyperconjugative structures along with the resonance from oxygen . is my logic wrong ?
ahh. was waiting for it .
thanks brother 😀
Excellent videos.. Please keep up the good work 😀👍
+Shamanth M.M. thank you
@@sachinranaiitb sir cld u plz upload a video on youtube of the imp ques to be done from the cengage books and what's the right way to read them. hope u won't disappoint us.
@@sachinranaiitb bhaiya organic series suru kardo na
At 16:32 you can actually see the sweat, that he's wiped off by his hands, on his fingers! Thanks a lot for doing this for us!!
Don't know why UA-cam recommended me this video today.
But one should see and learn watching this that success doesn't come overnight!
🎉🎉🎉🎉
18:55 By taking PEN and PAPER
Wow!
Swag dekho londe ka!!!🔥🔥
#respect...when other iitbombay guys are busy doing their own study and trying to make a good engineer......u r helping create lakhs of excellent engineers.
I think one day u will get 7M subscriber instead of the +nt keep it up 😃...........making such amazing vedios 😮😁😁😁😁
+Sonika Sheoran thanks.
🙄🤣🤣
East or West Sachin sir is the best👍👍👍👍
Aldehyde ketone. .
Also Pleaseeeeeeeeeeeeeeeeeeeeeeeeeeeeee
Shreyasi : Can u plz provide family wise compilation of reactions for P block? I would be really relieved....U inspire me everyday Bhaiya... Thank u so much :-)))
sir in the first que when we get nucleophiic benzene ring, why will it attack O2? doesnt O2 have free electrons around it..thus nucleophile would not prefer to attack it right?
Bhaiya you explain each and every step logically. Great work.👍❤️
Very helpful and excellent questions which are often not taken up at coachings . Thanks a lot Sir
thanks sir ,
pls do upload the videos of rest of the organic topics.👍
very very nice..... please if you can could add a video on biomolecules and polymer for JEE ADV
thanks a lot
i found it very helpful for preparation of JEE as all concepts are covered in very short time. Thank you☺
Bhaiya in the video at time 8:52 you R doing pinnacole pinnacolon ,so according to migratory aptitude instead of methyde shift there should be hydride shift
Good job bro it helped me in understanding
U deserve thousands of likes.... Keep uploading these videos... Thanks
Baiya apke ye sare lectures jisme apne hr chapter ke sare reagents cover kiye hai ye sare reagents sufficient hai kya
Bhaiya make a vedio on rotation. Basics like. About which axis torque = I alpha can be applued. COM or around axis
You sir, are a blessing in disguise for the ones preparing with self study. Huge thanks.
V . v. nice video..... wakai aap ek acche chemist h...
Sir how does Grinard Reagent chooses between C=O and same come compound containing O as hetero atom ?which place will it attack.. I mean which bond is weaker?
I will have to comment
One of the best revision videos
Awesome video
Thank you so much bhaiya 🙏🙏🙏🙏🙏🙏🙏🙏
videos bahut helpful h. :)
continue making the same.
if possible pls make a video on coordination compound,thermodynamics and probability before 10th may !
Very helpful video sir . Thank u😘 very much
bhaiya pls try and upload a video on biomol.and polymers before Jee advanced 2017 as these two topics are very crucial wrt jee and it would be of a great help. . .and Bhaiya ur way of teaching chem is just fabulous . thanks a lotfor all these beautiful video s.....
thank you very much sir.please upload more vidios on physical ,inorganic and organic as soon as possible because neet is no more far,
+Manisha Pati yes sure.
thank you sir
+Manisha Pati welcome
Amazing job! Keep it up bhaiya! Its damn useful for backlog covering students like me 😅
I really like these videos because my time does not waste here
Sir,
I have been watching all your chemistry and maths videos .It would be a big help if you could explain physics also (EMI, fluid mechanics, modern physics,wave optics)
The way you explain is just amazing.
Thanks again
Bhaiya how to know which hydrogen is most acidic please tell.....☝️🙏🙏
great job sir , keep making helpful video thanks a lot sir
Kahan college mila bhaiya aapko
Sir what a video its Amazing ....!!!!
Thank You Sir
Sir please can ypu upload more videos on short tricks in inorganic ? Thank you so much!
Sir at 15:33. H30+ is 2nd reagent right.So why are You taking it before the complete reaction of LiAlH4.i.e First the Compound should be attacked with 4 H- and Only then H3O+ should be considered right?.Please Clarify this.
great vedeo sir.please aldehyde ketones and acids ki go sari reaction Kara do
Nice very nice vedios by u thanks brother
Great work ..best explained ever...keep on doing it....thanks
Bhaiya at 8:31 why did you do methyl shift ?
It is already a 3° carbocation and after Me shift it turns into 2° carbocation.
??
He used the h+as the catalyst as we know every catalyst has to be removed after occurrence of any organic reaction he did me shift to remove h from oh attached to the carbon. If he didn't shifted the methyl and removed h+ from the adgecent carbon he will get an unstable reaction intermidiate.hope you found it useful
Bhaiya aise hi sabhi chapters ke videos bana dijiye.
excellent video sir
please upload a video on tricks on pnc and binomial thrm
very useful sir
could you make a video on stereo isomerism on octahedrl in complex compounds
thank you very much I was looking for the Right video on alcohol Revision. thank you ................................
How to know whick compound is electrophile and nucleophile
Superb bhayya..😊😊
is this revision lecture will help me to complete all the reactions dnd no need of other books for revision
Very good video, keep it up. Could you suggest me more UA-cam channels like yours. Preparing for Jee mains through self study. Need to follow good channels like yours in
abhi verma
Thank you, any other recommendations?
Hie. You really explain nicely but it would have been really very helpful if you could have made videos for neet aspirants too .
Most Awesome Course !!!!! Thank u ...... SIR !!!
Plzz phenols videos aur upload kijiye.... Sir....
the way u represent these reaction ,,,,I swear no one can represent I ve seen
u r the best bro.
please what u think important about thermodynamics please upload
+Subhrajeet Sahoo yes sure i shall.
OK thanks but quick
10 days for neet only😨😨😨
and rest of the organic part
Did u crack neet exam, how much u score?
Nice it is really helpfull to students
Dear sir..will you please provide videos on physics ,chemistry specified to state public service commissions...the questions that were asked in the particular examination is very static and factual..almost 80 percent.
You deserve more than likes amazing😚😚😚
Where will d grignard attack if both ketone and ester group is present..ppplzz say
deserve 100000++++++
+A J thanks.
You are a genius
At 8:10 tertiary carbocation is more stable, then why methyl shift will take place?
Too late to answer but just for the sake of other people, the methyl shift takes place as carbcation is stable on the 1st carbon and then plus charge shifts to adjacent carbon and simultaneously O donates its lone pair, and then h+ gets removed. He shortened the mechanism just for sake of simplicity.
But the 2 degree. Carbo action was more stable then why wont shift decrease its stabilty
Also why dint the h shift ?
@@jasjappansingh2170 because stability due to lone pair is more than anything else
@@meetshah6538 but instead of methyl shift, hydride shift could have taken place according to migratory shift order
Your videos are always contradicting to Expectations vs Reality. You hope of getting 100 likes and end up getting more than 1000 likes😁
Bhaiya phenols and ethers ke liye bhi banao na plz
what is that under mg ( under arrow mark)? i cant understand > is it h2o?
pls upload such revision videos....for the rest topics also for aldehydes and ketones n all!
Rohit Sahu yes I shall be uploading
sir plz if possible can u explain bouvealt blanc reduction of amide...plz
What about other rxns of alcohols in ncert. Are they not imp for JEE adv. You mentioned all rxns so asked
your writing speed is so fast brother...😀 the way u explaining concept is great.
+Moin mansoori thank you.
SIR APKE NOTES KI BOOK MILEGI KYA
thanks sir..plzz amines ka ek video
+Barsha Acharya sure.
yes i need it too and thanks a lot for other for other videos your are really doing a great job bro keep it up!
please upload videos on EMI and Magnetism asap its very urgent
in your 3rd point which reagent you have used along with mg ?
Ether Et2O
bro at 8:45 in that reaction why there cant be hydride shift
Same doubt
Very helpful, thank you very much
Plzz upload videos on phenols and their preparations plzz
Hey love your videos !
They really help a lot...
Could you please upload a video on aldehydes and ketones
Really need it. Thank you!😊
Sir plzzz make the video of nulecophile and electrophile
Will be thankful to you forever
8:40 , the carbocation was already 3degree
Then why rearrangement take place??
Plz explain.
Pinacol pinacolin Rearrangement Bro🙂
ua-cam.com/channels/EpHagvc6KZtOXsqq0agUuA.html
Sir lone pair of chlorine is in resonance with benzene so how can we use mg in presence of ether as u told that it is weak and it will not form grignard reagent
Sir you got 115/120 math marks in mains can you upload videos on maths for mains and advance
sir I m NEET aspirant I found these to be smwat tough ACC to NEET
is it so???
u r providing these videos ACC to jee??
+sanjeev mital nothing's tough in the world.
Jo aata hai voh aasan hota hai, jo nahi aata hai voh hamesha hard.
Sachin Rana - IIT Bombay Hats off to you sir..
sir at 7:46 (approx ) in the example which you were discussing , there is an alcohol already formed . alcohol's hydrogen is acidic . will the second mole of grignard reagent choose to abtract the acidic hydrogen ?
+ganesh nagarajan that's awesome thinking. But since we get the protic solvent later; we need to proceed with the reaction.
how sir . we first hyrdolyse it and then put in the next mole right . so when an alcohol is formed doesnt acid base reaxn favour over substituition ??
At 7:41 won’t the second R- try to snatch H+ from 2 degree alcohol formed, as R- is a strong negative charge.
Nice video sir
sir cld u plz upload a video on youtube of the imp ques to be done from the cengage books and what's the right way to read them. hope u won't disappoint us.
these questions are very hard.. is such questions asked for neet??
Plz upload for ether n phenol toooo
Bro is this sufficient for theory.
sir at 8:50 (approx) , wont hydride shift take place as in pinacol pinacolone rearrangement ? isn't hydride shift easier than methanide shift?
+ganesh nagarajan no. The group which is more releasing has a higher chance of shift.
sir but while shifting takes place methanide shift is lot slower than hydride shift due to the bulky nature of methyl group and moreover if you shift the hydrogen you get a even more stable carbocation with three extra hyperconjugative structures along with the resonance from oxygen . is my logic wrong ?
@@ganeshnagarajan5488 you are absolutely right bro
. .
VERY GOOD VIDEO OF ALCHOLS
pllzz answer me soon that is this revision lecture is enough for the neet student and covers all the rections
+Parshvi Nahar yes to a certain level it is enough. You can check out my notes.
sir at 8:19 according to migratory shift order hydride shift should occur or is it the way you did?
yeah i think its wrong
hats off bro 😍😍🙌
Sir I have a doubt that when to attack H- on Oxygen atom in ester part
bhai aapke concept aur unko batane ka style dono kafi diffrent aur bahut mazedar hai....bhai plz solution ka vdo upload kar digiyae na plz...
+akroor singh Kovid thank you
lv u sir
very interesting lecture
how mg/et2o broke the resonance stablize bonds
At 8:10 the tertiary carbonation I s more stable the why methyl shift😕
Backbonding
Thanku bhaiya
Brother at 8:35 why did you perform a methyl shift even though H- ion ( hydride ion) is also present?
it should be an Hydride shift right?
plz reply