I’m so grateful that I found your channel, you are the best person to explain the organic chemistry in the entire universe, and you’ve made me loving it 💕thank you for everything
can you explain something that I didn't understand in my textbook? That the bond strength is inversely proportional to the carbon radical stability. I mean that the more stable the resulting radical, the weaker the bond. How??
It sounds like it's saying that the more stable radical intermediate is MORE able to be present as a radical in solution. Therefore, any resulting bond it forms will be weaker. As it was happy enough in its radical form. The converse of that would be a less stable radical intermediate that happily forms a new bond that is stronger and more likely to be present in solution.
Leah, the scrolling border around half way was very distracting, especially for us neurodivergent folk. I had get some tape to put on my computer to block it out. Please fix it to static for next stream 🙏
Thank you for letting me know, I have ADHD and hadn't considered it. I will change it up next time (or keep it up for a shorter amount of time). Thank you and I hope that with the tape on you were able to enjoy the lecture
Grab the Radical Reactions Practice Worksheet + Session Notes at Leah4sci.com/orgolive (+ heads up for upcoming sessions)
I've never clicked the Like button faster, thank you so much for your time, dedication and help!
I appreciate it so much! So glad you found this session helpful. Hoping to see you live on the next one (Monday)
I’m so grateful that I found your channel, you are the best person to explain the organic chemistry in the entire universe, and you’ve made me loving it 💕thank you for everything
Wow, thank you for your kind words! I'm so happy that I've been able to help you love orgo (it's my secret mission!)
thank you for this amazing video lesson!!
You're very welcome!
can you explain something that I didn't understand in my textbook? That the bond strength is inversely proportional to the carbon radical stability. I mean that the more stable the resulting radical, the weaker the bond. How??
It sounds like it's saying that the more stable radical intermediate is MORE able to be present as a radical in solution. Therefore, any resulting bond it forms will be weaker. As it was happy enough in its radical form. The converse of that would be a less stable radical intermediate that happily forms a new bond that is stronger and more likely to be present in solution.
Looking forward for more content like this ❤️
Look out for my weekly (weekend) poll to help me choose the upcoming Monday's topic
@@Leah4sci Will do 👍
Leah, the scrolling border around half way was very distracting, especially for us neurodivergent folk. I had get some tape to put on my computer to block it out. Please fix it to static for next stream 🙏
Thank you for letting me know, I have ADHD and hadn't considered it. I will change it up next time (or keep it up for a shorter amount of time). Thank you and I hope that with the tape on you were able to enjoy the lecture
Thanks! I finally became a member. Happy to finally have sent you some $$ after the years i've been in chemistry in and out.@@Leah4sci
Yep
:)
I’d say “radical hydrohalogenation”..
Good point, adding HX is a hydrohalogenation reaction