The way u represent is tremendously beautiful, understandable, clear , easy language! Hope to see more basic chemistry vedios of you Chemistry lovers waiting
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
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 😀😀
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 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
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
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
underrated channel for teaching ever....One of the best lecture I ever had👏👏
The way u represent is tremendously beautiful, understandable, clear , easy language!
Hope to see more basic chemistry vedios of you
Chemistry lovers waiting
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?
One of the best..tutor I had ever found on RUclips..Great Man..🙏🏻🙏🏻🙏🏻🙏🏻🙏🏻
Wow, really I am big fan of your explanation 🎉🎉🎉🎉❤
Mr Najam my Favorite Teacher ☺️🥰 I love your Video So so so much. I'm from Ethiopia
😊people I love❤😊
Thank you sir for this video because i am see this video before 1 day of exam
Outstanding explanation in less time ❤❤❤
Your voice is rulling over my syllabus 😎
It is simply the best explanation of the concept ever seen ⭐⭐⭐⭐⭐
WOWW SIR! THANK YOU SO MUCH. I discovered this 2 days before the exam and was a savior. Thank u so much sir.
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
Amazing Concept Explanation
Sir please teach whole chemistry subject
Please make elimination video
Plz make on electrophilic reaction
All my concepts are cleared by watching this video 👍
Amazing Sir.... this video very helpful to me...Tqq Sir...🎉😊😊
Amazingly explained 👏 👌🏻
Highly appreciate your efforts 👌🏻 😊
Sir pls make one shots , it will be very useful during exam time and one shots are good for productive revision of a chapter .
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
Jazakallah khair
This is the best explanation i have heard❤
Your explanation is soo good
Tqsm
My 8 minutes r worth it 😃
Finally i found that video which makes easy sn1 and sn2 thx a lot
Thank you so much for your fabulous video
Hats off to you sir.... Brilliant 👍The way you teaching is just amazing 👏students need teachers like you for bright future
Gud gud gud, nice lec and osm explanation, thnx sir for your efforts 🥰🥰🥰
Your explanation is spellbound sir👏💐
Sir thanku so much, no words to thank you sir❤
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?
Salam Mr Najam thank you & best wishes from Algeria to you & your family.
✅
W salam!!!
love and respect!!!
❤️🤲
fantastic teaching Sir i am fully impressed
Thank you so much,
you've helped me a lot.
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.
Thank you soo much for these vedios
Wow.. thankue so much sir.. amazingly explained
Love your video ❤
Understood it super well
😊😁thank you so much
Life saviour
loved the explanation seriously
Thank you sir😌 for clearing my doubts.
Thanx sir! U saved ma precious time
Very very helpful video 👍👍👍👍👍👍👍👍👍👍👍👍👍
Explained Way better then the teachers pretending to be teaching advanced level before teaching the base carefully
Superb explaination😊
Very helpful.Thank you so much.😊
Thanx bro for this video but pls make one video on electrophilic substitution❤
Literally amazing explained🤝❤️
great video helped me with my exams
Outstanding explanation
Thank you,Sir.
I understand finally what nuclephile rxn mean
Thank you so much 🎉😊sir ji
Ironically explained 😮
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
Tq Sir For Nice Explanation
How can you know that this is a strong nucleophilic reaction?
Weak electronegative means strong nucleophile and vice versa
Thank you thank you sooo muchhhh😊
Masterpiece ❤❤
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
beautifully done
Please explain how sn1 is favoured by weak nucleophile,,,,I couldn't understand
Even I don't understand
Thank you a lot 💘🎉
Thanks bhaiya ❤
Best lecture for us
Mashallah ❤❤
love u uncle ❤
Wow great ❤
Your voice is stronger than the nucleophile 🤌💪💪😲
Thanq , Thanq so much ❤
Firstly
Secondly
Thirdly
Fourthly
Fifthly
Sixthly
Seventhly
😂 New numbering system
No doubt content is good❤
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
Please do full length videos
Nice and perfect 👍👍
well appricated
Tq bro 💗😢
Amezing 👍
Sir can we write as it is in the exam
Thanks 🙏 sir❤
good concept clarity
Thank you sir amazing video
2:04 sn1 reaction
Your explanation good
Outstanding sir
❤️u deserve more🫶🏻
thank you so much ...u help me lot sirrr😭😭😭😭😭😭👏🏻👏🏻👏🏻👏🏻
Excellent!
Best explanation i have ever seen😮
how do you determine a strong and weak nucleophile???
Bases tend to be strong and acids tend to be weak nucleophiles
Please make videos on physical chemistry chapter wise ,,it ll more helpfull for students,,,puc students
Thank you so much
Please make a video what type of qs came from it
Super super ❤
thank you so much sir... tomorrow is my exam 🎉😊
Excuse me sir, please put video for Electrophilic substitution reaction also
Good explaination
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
if there is no carbocation formed in sn2 then how the nucleophile attack the carbocation in sn2
your teaching method is best, but time is short, try to teach long please