Ms.leah, you dont know or understand how many students you have helped grasp organic chemistry, youre literally the OCHEM angel and we speak of you highly, youre a legend in my univeristy, thank you so so much for what you do!
Thank you so much, I am honored and humbled by your compliment. I struggled with organic chemistry in undergrad and strive to make videos that will prevent others from having to go through what I did. I hope it's working :)
@@Leah4sciI'm doing EV research using super resolution microscopy, so nothing related 😂 I am just really passionate about organic chemistry, and I'm hoping to pursue a PhD in the field soon!
Oh wow that sounds really intense and quite fascinating, I hope you go to work every day excited to play with the 'fun toys'. Wishing you the best with your PhD
this was so incredibly useful, your videos are carrying me and all my friends through orgo right now. thank you so so so so much! wish you were my teacher :')
Im absorbing the information! Even if it's a little ahead of my current knowledge. Cant thank you enough. Your explanations and descriptions just make sense! I LOVE CHEMISTRY!!!!
SN/E is definitely something to understand more than memorize for the DAT. Hope this video helped and be sure to check out my alkene and alkyne playlists for your upcoming studies. I'm actually preparing to publish an alkyne video next so keep an eye on your notifications.
SN2 cannot happen with a tertiary leaving group because there is too much hindrance blocking the attack. However, if the leaving group on a tertiary carbon is not attacked directly, and the beta carbon's H is accessible, and E2 is not only possible, but quite desirable due to creating a highly substituted and therefor stable pi bond. This is in accordance with Zaitsev's rule
Ms.leah, you dont know or understand how many students you have helped grasp organic chemistry, youre literally the OCHEM angel and we speak of you highly, youre a legend in my univeristy, thank you so so much for what you do!
Thank you so much, I am honored and humbled by your compliment.
I struggled with organic chemistry in undergrad and strive to make videos that will prevent others from having to go through what I did. I hope it's working :)
Thank you so much mam@@Leah4sci
I have graduated almost 5 years ago now, and I still watch these videos. They're so good for keeping your fundamental ochem sharp!
Oh wow that's amazing! What are you currently studying/doing that you're keeping sharp in orgo?
@@Leah4sciI'm doing EV research using super resolution microscopy, so nothing related 😂 I am just really passionate about organic chemistry, and I'm hoping to pursue a PhD in the field soon!
Oh wow that sounds really intense and quite fascinating, I hope you go to work every day excited to play with the 'fun toys'. Wishing you the best with your PhD
I needed this. We're currently in this section, and I'm so confused. Because of you, I have an A in O Chem! ❤
Love that this came at a perfect time for you and honored to be a part of your journey! YES to getting an A!
this was so incredibly useful, your videos are carrying me and all my friends through orgo right now. thank you so so so so much! wish you were my teacher :')
So glad I can help! If you need help as you close in on your finals reach out to me at leah4sci.com/contact for more resources.
U are my time saver and one of the best doubt solver thank you ma'am....❤
Glad to help
I have my Orgo I final tomorrow and I am currently at an 89. Shooting for an A. Wish me luck guys
So close! wishing you the best to get that A
@@Leah4sci I got an A on the Final, and an A overall! Thank you for your informative videos!
This channel is highly underrated.
Aww, thank you!
Ur helping me to get out from depression .
Thanku so so much❤
Luv u
I'm so happy to be a help for you during such a tough time. Sending hugs.
Leah4sci > The Organic chemistry tutor
Thank you, I appreciate it! The Organic Chemistry Tutor is pretty good :)
I agree
I love your videos so much you are such a blessing, it helps me so much in my learning process ! I always watch your videos
I'm so glad to hear that! And thanks so much for your kind words.
WOW!!! I have my midterm THIS THURSDAY on this, this just came out!
Glad this came at the perfect time for you! I have a full series on SN/E reactions here leah4sci.com/sne
Best of luck on your exam
Im absorbing the information! Even if it's a little ahead of my current knowledge. Cant thank you enough. Your explanations and descriptions just make sense! I LOVE CHEMISTRY!!!!
You're very welcome! Chemistry is an awesome subject
Thankyou mam , this helps me lot to understand deep and
faster solving for JEE Examination.❤
So glad to help!
Currently studying for the DAT. Perfect timing bc this was so confusing for me! Now off to learn alkene alkyne mechanisms 😂
SN/E is definitely something to understand more than memorize for the DAT. Hope this video helped and be sure to check out my alkene and alkyne playlists for your upcoming studies. I'm actually preparing to publish an alkyne video next so keep an eye on your notifications.
New content :0 I don't even need Ochem anymore and imma watch
Wow, glad you're still enjoying my videos even after finishing organic chemistry
perfect timing bc i have an exam on this in an hour 😂
Oh wow, hope you had enough time to practice a few examples so you can apply it on your exam
Well done
thank you!
In the second problem at the end, how can it be E2? The base is strong so it should be both E1 and SN1 at the same time
Strong bases will not allow a carbocation to form. Thus a strong base automatically rules out SN1 and E1 reactions
might as well give you my tuition
Sure! 😁 Leah4sci.com/join
best explanation
Glad you think so!
Simply amazing 😊😊😊
Thank you!
I’m confused
How can a tertiary carbon go with E2
When everyone say it’s not possible
I don’t understand
SN2 cannot happen with a tertiary leaving group because there is too much hindrance blocking the attack. However, if the leaving group on a tertiary carbon is not attacked directly, and the beta carbon's H is accessible, and E2 is not only possible, but quite desirable due to creating a highly substituted and therefor stable pi bond. This is in accordance with Zaitsev's rule
Hey, Liah!! Can u make a video on ring expansion? Thanks :)
(New sub)
Hey! Thanks for subscribing. I do have one on Ring Expansion via a hydride or methyl shift. To watch, visit my site at leah4sci.com/hydride-shift/
Perfect,
Thanks