Sir please upload class 11 and class 12 playlists , as it will be more organised and encourages the students to complete a chapter by watching your playlists rather than just learning a small chunk from a chapter by watching a single video . It will be more useful if the playlist have one shots as well
There is possibility that strong nucleophille can directly replace the weak nucleophille. But it is also possible that nucleophille can join the compound and then the weak nucleophille gets detached hence there are 2 type -SN1 and SN2
I guess there's a small mistake oh doesn't directly attack in sn1 first the h2O(weak nucleophile) attack on the carbocation and then it gets de-protonized to form oh but if we directly add oh we get a sn2 rxn and form a transition state 😀😀
i can't explain how this video is helpful to me i clearly understood the topic and i have one question here can i say that the inversion of configuration in sn2 mechanism is also 50% inversion as like one of the configuration in sn1 mechanism? pls answer this
Sir , in your Sn2 reaction explanation , you showed methyl chloride . It is not a primary alkyl halide , I think it should be ethyl chloride , sir please make amendments .
is this substituion different from those which occur in metals? like in metals also one strong metal displaces a weak metal from its molecule. Like sodium displaces Potassium in a displacement reaction
In sn1 reaction you took oh for nucleophiles as an example But can we also write H2o(water)as a nucleophiles. I feel confuse to take nucleophiles between oh and h2o. Please explain me someone
Element consists of single type of atom in non bonded state , say for example carbon element consists of carbon atom only . While ,a molecule consists of two or more different types of atom in bonded state, say for example NaCl is a ionic molecule consists of Na atoms and Cl atoms formed by ionic bond
because chloride has only partial negative charge rather than the complete negative charge of the hydroxide, the chloride only has a partial negative because its extremely electronegative compared to the carbon that it is bonded to thus attracting carbons electrons and gaining a small negative charge while inducing a small positive charge on the carbon atom itself. hope you understood.
Sir , in your Sn2 reaction explanation , you showed methyl chloride . It is not a primary alkyl halide , I think it should be ethyl chloride , sir please make amendments .
Sir , in your Sn2 reaction explanation , you showed methyl chloride . It is not a primary alkyl halide , I think it should be ethyl chloride , sir please make amendments .
No methyl chloride is primary alky halide as it is connected to a primary carbon which means halogen is attached to only one carbon thus it is primary alkyl halide
The only page which teaches chemistry better the the teachers pf jee and neet
Thankyou 😊
Thank you so much I got all information about SN1 and SN2 reaction once again thank you 🎉😊😊
Thank you, I finally understood this topic !! Can you do a video on the Elimination reaction E1 and E2?
Sir please upload class 11 and class 12 playlists , as it will be more organised and encourages the students to complete a chapter by watching your playlists rather than just learning a small chunk from a chapter by watching a single video .
It will be more useful if the playlist have one shots as well
Please make elimination video
Plz make on electrophilic reaction
But you only told that a strong nucleophile replaces a weak nucleophile then why in SN2 reaction it is not possible for replacement
Sn2 is strong and sn1 is weak
It replaces bro for ex CH³Cl+NaOH = CH³OH+ NaCl
Actually sn1 and sn2 reaction is takes place by replacement here note then5 point carefully that is rearranged
There is possibility that strong nucleophille can directly replace the weak nucleophille. But it is also possible that nucleophille can join the compound and then the weak nucleophille gets detached hence there are 2 type -SN1 and SN2
because in sn1 rxn the tert butyl bromide firstly ionises and made carbonation Then a nucleophile attacks on it.
I guess there's a small mistake oh doesn't directly attack in sn1 first the h2O(weak nucleophile) attack on the carbocation and then it gets de-protonized to form oh but if we directly add oh we get a sn2 rxn and form a transition state 😀😀
Please explain me
Wow, really I am big fan of your explanation 🎉🎉🎉🎉❤
Thanx bro for this video but pls make one video on electrophilic substitution❤
Jazakallah khair
Hats off to you sir.... Brilliant 👍The way you teaching is just amazing 👏students need teachers like you for bright future
i can't explain how this video is helpful to me i clearly understood the topic and i have one question here can i say that the inversion of configuration in sn2 mechanism is also 50% inversion as like one of the configuration in sn1 mechanism? pls answer this
fantastic teaching Sir i am fully impressed
Highly appreciate your efforts 👌🏻 😊
Your explanation is soo good
Understood it super well
😊😁thank you so much
Gud gud gud, nice lec and osm explanation, thnx sir for your efforts 🥰🥰🥰
Explained Way better then the teachers pretending to be teaching advanced level before teaching the base carefully
Thank you so much for your fabulous video
Salam Mr Najam thank you & best wishes from Algeria to you & your family.
✅
W salam!!!
love and respect!!!
❤️🤲
This is the best explanation i have heard❤
thank u u u u u u u . U deserve nobel prize not these professors who care too much about their titles and ego
What?
Please make videos on physical chemistry chapter wise ,,it ll more helpfull for students,,,puc students
Your explanation is spellbound sir👏💐
Outstanding explanation
Thank you,Sir.
your teaching method is best, but time is short, try to teach long please
Thank you soo much for these vedios
great video helped me with my exams
i think that you made a mistake in the primary alkyl halide as it did not contain any alkyl group, while u were explaining SN2.
Ch3 is alkyl group
Your voice is stronger than the nucleophile 🤌💪💪😲
underrated channel for teaching ever....One of the best lecture I ever had👏👏
Life saviour
loved the explanation seriously
Thank you sir😌 for clearing my doubts.
Wow.. thankue so much sir.. amazingly explained
Sir , in your Sn2 reaction explanation , you showed methyl chloride . It is not a primary alkyl halide , I think it should be ethyl chloride , sir please make amendments .
Love your video ❤
Superb explaination😊
How can you know that this is a strong nucleophilic reaction?
Thank you a lot 💘🎉
Very helpful.Thank you so much.😊
Please make a whole playlist of this chapter
Literally amazing explained🤝❤️
Please make a video on distinguish tests and numericals tricks for physical chemistry class 12th
thank you so much sir... tomorrow is my exam 🎉😊
is this substituion different from those which occur in metals? like in metals also one strong metal displaces a weak metal from its molecule. Like sodium displaces Potassium in a displacement reaction
Thank you so much 🎉😊sir ji
Best lecture for us
Very very helpful video 👍👍👍👍👍👍👍👍👍👍👍👍👍
Thankyou...Elimination reactionn pleasee !!
Your explanation good
Sir please aromatic er full topic er class den,such as nitration sulphonation,halogenetion...
In sn1 reaction you took oh for nucleophiles as an example
But can we also write H2o(water)as a nucleophiles.
I feel confuse to take nucleophiles between oh and h2o.
Please explain me someone
Thank you so much sir
Plz stereochemistry of SN1 SN2 E1 E2
Sir please tell difference between element and molecule
please sir
Element consists of single type of atom in non bonded state , say for example carbon element consists of carbon atom only .
While ,a molecule consists of two or more different types of atom in bonded state, say for example NaCl is a ionic molecule consists of Na atoms and Cl atoms formed by ionic bond
Firstly
Secondly
Thirdly
Fourthly
Fifthly
Sixthly
Seventhly
😂 New numbering system
No doubt content is good❤
Outstanding sir
Stay blessed ❤
2:04 sn1 reaction
Nice and perfect 👍👍
Wow great ❤
Still watching this 100th time still can't exactly remember it😭
Tq
Plzz make videos for JEE I know it will be tough but can you do it?😢
Amezing 👍
Tq u so much sir
If carbocation is not formed in sn2 reaction then how nucleophile is attacks in back side
Thanks
Thanks sir
Plz sir we want biology so upload some vdo class 12
Sir from where you are
Sir Order of rxn ka tracks bataye sir??
Please uplod full chapter halogen derivative
Best explanation i have ever seen😮
Sir electrofilic substitution reaction send...
Why does hydroxide become more strong nucleophile than chloride?
because chloride has only partial negative charge rather than the complete negative charge of the hydroxide, the chloride only has a partial negative because its extremely electronegative compared to the carbon that it is bonded to thus attracting carbons electrons and gaining a small negative charge while inducing a small positive charge on the carbon atom itself. hope you understood.
Nice 🙏
thank you so much ...u help me lot sirrr😭😭😭😭😭😭👏🏻👏🏻👏🏻👏🏻
❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤Seriously I love your teaching ❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤
7:40
Bhai apne SN1, SN2 dono me hi strong Nu- (OH-) le liya
In Sn1 reaction you said 1 step is slow and then you also said that Sn1 reaction is faster in 3 > 2 > 1
becoz In SN1 reaction 1st step is Rate determinig step thats why this is slow and in tertiary halides it show overall fast reaction than 2nd nd 1st
@@kalpanadeshmukh-do6nh ooh okieee
Bros English at peak
5:04 sn2
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Sir please provide notes 🙏🙏🙏🙏
Where is nucleophilic video
Hmm
❤❤❤❤❤❤❤❤❤❤❤❤❤
op ❤❤
🙏🙏🥰
Please Hindi me v explain kiaaa kijiye..
Please make in Hindi or you can doubbed it too
Strong people always rule over weak people LMAO!
too much error in spelling
Please do full length videos
Sir , in your Sn2 reaction explanation , you showed methyl chloride . It is not a primary alkyl halide , I think it should be ethyl chloride , sir please make amendments .
Methyl chloride is a primary alkyl halide kiddo, check Google once and you will get it.
Thank you so much
7:42
Sir , in your Sn2 reaction explanation , you showed methyl chloride . It is not a primary alkyl halide , I think it should be ethyl chloride , sir please make amendments .
No methyl chloride is primary alky halide as it is connected to a primary carbon which means halogen is attached to only one carbon thus it is primary alkyl halide