Perfect timing on this one but wow it sounds like you want me to create a video for EVERYTHING on your exam. Actually I already have that and more here: leah4sci.com/join
I'm sorry, but I don't offer tutoring over social media. If you ever find you need help with questions like this again, I recommend joining the organic chemistry study hall. Details: leah4sci.com/join or contact me through my website leah4sci.com/contact/
I'm sorry, but I don't offer tutoring over social media. For help with questions like this and more, I recommend joining the organic chemistry study hall. Details: leah4sci.com/join or contact me through my website leah4sci.com/contact/
If you look at the completed energy diagram at the end of the video, you'll see a different structure drawn at each peak and valley of the curve. The transition state, specifically, is the highest energy 'version' of the molecule reacting. It is where any bonds breaking or forming are drawn as partial bonds. It shows the molecule in the midst of its change, and not as a stand-alone molecule able to be isolated.
I just have a little confusion... in sn1 the more stable carbocation I.e the 3° will have a higher reaction rate but why does it take more time to form the less stable 2° carbocation in the RDS ?? It's been bugging me fr a while now...but I can't seem to find any explanation fr this M I actually looking from the wrong perspective ?? Or is there like a slightly different E.P graph fr 2 ° carbocation following SN1
I'm sorry, but I don't offer tutoring over social media . For help with questions like this and more, I recommend joining the organic chemistry study hall. Details: leah4sci.com/join or contact me through my website leah4sci.com/contact/
@@Leah4sci such a nice diagram. I'll have to watch this again... One thing I wanted to ask is could you point me in the direction of stereo selectivity.... That is something I find simply mind bending. Not the isomers themselves... But then something like thalidomide... It didn't matter if you selected for the isomer as it would rearrange in the body! Ahhhhh!!!
Negativity doesn't always imply strong attacker. Cl- is actually a very weak base making it impossible to grab H for an elimination reaction. See my Nucleophile vs Base video for more on this leah4sci.com/acidbase
I'm a 18yr old IIT-JEE aspirant from India. The JEE(A) is the toughest test in India. The teacher who taught me Sn1 Sn2 E1 E2 Ei is a 62 year old lady teaching for over 3 decades and your explanation was way better than hers. Thanks, grateful 🙏
Love you, Leah. You’ve been a lifesaver for me in Orgo. I used your materials to prepare for my MCAT as well. :)
Awesome! Have you registered for the newsletter yet? If not, feel free to contact me through my website: leah4sci.com/contact
Thanks a lot
Love from India
you're welcome
concepts cleared ....thanks
love from India.
Glad it helped!
Don't know how to thank Ma'am
Just amazing
Masha Allah
Thank you very much for this lecture
You are so welcome!
😇♥️
Thank you, you explain so well!
You're very welcome!
It clear my all doubt ..thaks❤️
Glad to hear that!
Thank you so much, excellent explanation 🧠✨
You're very welcome.
Wow you taught it amazingly. Love from India🇮🇳
thanks so much
Thank you very much
You are welcome!
amazing teacher amazing narrator amazing explainer you r a gift from god to all of humanity
Aww thanks so much, I'm glad the video resonated with you.
Thank you very much. Your explanation is very clear🎉
Glad it was helpful!
ty for this awesome video, i was able to grasp everything super quickly!
You're welcome, I'm so glad it helped!
Thanks a lot one more time . Lots of blessings from India.
You're very welcome!
May God bless you! You are the best!
Wow, thank you!
Very well explained ❤
Thanks so much!
Thank you Ma'am! ❣
You're welcome 😊
So cute explanation ❤❤❤
Glad you think so!
Explained very clearly👍👍
Thank you! 🙂
Thanku...very much for beautiful explanation..😊😊
Love from india❤
You're so welcome!
Great and clear explanation.... Searching for this and rightly got here...thanks...please make more informative videos like this
Glad it was helpful!
Thank you, Leah!
You're very welcome!
thank you for the video
You're welcome!
Thanx alot u explain so well
Happy to help!
thank you I actually have a test on this on Wednesday. Could you do one for Sn2 E1 and E2? and maybe chiral carbons and all of that stuff lol
Perfect timing on this one but wow it sounds like you want me to create a video for EVERYTHING on your exam. Actually I already have that and more here: leah4sci.com/join
Thank you very much leah🥰
You're so welcome
Tqq so much. Dear😊
You're welcome 😊
what is the energy profile diagram of acid catalysed dehydration of t-amyl alchohal ?
it undergo wiyh E1 mechanisms...
I'm sorry, but I don't offer tutoring over social media. If you ever find you need help with questions like this again, I recommend joining the organic chemistry study hall. Details: leah4sci.com/join or contact me through my website leah4sci.com/contact/
I am searching for this video. Thanks a lot mam
You're welcome 😊
Wonderful explanation. Thank you soooo much!!
You're very welcome!
GREAT THANK YOU
You are so welcome!
Thank you leah!
You're very welcome
Thank you so much ❤️😊
You're very welcome
In the energy profile diagram of solvolysis rxn , I got to know that there will be 3 peaks/humps , why so? Please reply🙏🏻
Every step has a transition state, that is the peak. If you study the reaction and know how many transitions you have, you'll easily find your peaks
thanks leah , very helpful
You're very welcome
THANKU🥰🥰🥰
You're so welcome!
Your explaination is clear thanks a lot mam🤗
You're very welcome 😊
Thanks Mam
You're welcome 😊
Hey Leah, do you mind showing some energy profiles leading to formation of alcohols from alkyl halides
I'm sorry, but I don't offer tutoring over social media. For help with questions like this and more, I recommend joining the organic chemistry study hall. Details: leah4sci.com/join or contact me through my website leah4sci.com/contact/
Why was the way the structure was drawn, changed only during TS?
If you look at the completed energy diagram at the end of the video, you'll see a different structure drawn at each peak and valley of the curve. The transition state, specifically, is the highest energy 'version' of the molecule reacting. It is where any bonds breaking or forming are drawn as partial bonds. It shows the molecule in the midst of its change, and not as a stand-alone molecule able to be isolated.
I just have a little confusion... in sn1 the more stable carbocation I.e the 3° will have a higher reaction rate but why does it take more time to form the less stable 2° carbocation in the RDS ?? It's been bugging me fr a while now...but I can't seem to find any explanation fr this
M I actually looking from the wrong perspective ?? Or is there like a slightly different E.P graph fr 2 ° carbocation following SN1
I'm sorry, but I don't offer tutoring over social media . For help with questions like this and more, I recommend joining the organic chemistry study hall. Details: leah4sci.com/join or contact me through my website leah4sci.com/contact/
Very Helpful vedeo
Awesome, glad I could help!
Thanks mam
Most welcome 😊
Cool thanks.
you're welcome
@@Leah4sci such a nice diagram. I'll have to watch this again... One thing I wanted to ask is could you point me in the direction of stereo selectivity.... That is something I find simply mind bending. Not the isomers themselves... But then something like thalidomide... It didn't matter if you selected for the isomer as it would rearrange in the body!
Ahhhhh!!!
Thx mam
You're so welcome!
Thanks you
You're very welcome
Since Cl- is negative, it is a strong attacker. Then it should be E2, why is it SN1?
Negativity doesn't always imply strong attacker. Cl- is actually a very weak base making it impossible to grab H for an elimination reaction. See my Nucleophile vs Base video for more on this leah4sci.com/acidbase
Potential Energy diagram Sn¹ mechanism
?
I'm a 18yr old IIT-JEE aspirant from India. The JEE(A) is the toughest test in India. The teacher who taught me Sn1 Sn2 E1 E2 Ei is a 62 year old lady teaching for over 3 decades and your explanation was way better than hers. Thanks, grateful 🙏
Wow, glad I could help!
so how's it going?
Carbocations cannot be isolated…..why she said it canbe isolated
I believe I said the carbocation intermediate can be isolated. That doesn't mean it's stable, but it's not as fleeting as the transition state.
@@Leah4sci ma'am wat i meant is carbocation is unstable n cannot be isolated.
@@saumyagaur3500 any reference for this?
Thanx alot u explain so well
You're welcome 😊