You taught me about chemical bonds, Acids, formal charges etc while studying in my home country. Now I am a 2nd Year Pharmacy student, still here. Thanks a lot. COOL!
Thank you for everything!! I got sick for a couple days and it was enough to make me fall behind during the hardest part of the course. I've been working every day to catch up and it's only possible because of your videos. You're an excellent teacher and thank you for sharing your videos for free. I might end up grabbing your premium course for the rest of the semester... I just wish I had started with your premium course from the beginning of the semester!!
Nice video Please also mention the effect of electron withdrawing grp such as phenyl carbonyl group that increase the rate of reaction As transition state becomes more stable
I’m doing my pre medical program and have come across your videos recently. Life changing videos u’ve got. Let’s get through this final stage together!!!!🙌
Hi Chad, thanks for all you do. Quick question, what is the difference between this orgo playlist and the other one (the first video of chapter 7 in this playlist is called "7.1a introduction to sn2 reaction". Thanks!
Hello Allan! The largest difference is the format. I'm using a whiteboard in these whereas I used powerpoint and a green screen in the old playlist. Many requested using a whiteboard. Outside of that there are some small differences in content here and there and I've broken up the material differently as well. For example here I cover SN2 reactions all in a single lesson that is close to 30 minutes long, whereas in the old playlist it is covered in two lessons totalling roughly 22 minutes. With writing everything out on the whiteboard the new playlist tends to be a little longer in duration as well. Hope this helps and Happy studying!
@@allan7720 Awesome! Be sure to begin by downloading the study guides before you begin a chapter and the Complete Reaction Summary. Then take full advantage of the quizzes, chapter tests, final exam rapid reviews, and practice final exams. Happy Studying!
Awesome Alyssa and I'm glad you're enjoying the Ultimate Bundle! It is truly amazing that technology makes it possible to deliver so much value for such a low price. I can't imagine what learning in a pandemic would have been like even 10 years ago. Happy Studying!
Sir we commonly say that a weak acid has a strong conjugate base .....as well as nucleophilic strength of a nucleophile is also decided by how much weak acid is using in the reaction ...... When we use KOH in the presence of water, major product is due to substitution reaction ......while KOH in the presence of Alcohol reaction shifts towards elimination reaction .....it means in water a good nucleophile is produced but in alcohol a good base is produced.....in both cases alcohol is slightly acidic than water ....is it the peculiar behavior or my concept about strength of base and nucleophile is wrong? Looking for your guidance thank u
@@ChadsPrep Thanks for answering! In the video you are telling "... And when you just double the volume of solvent, but kept the numbers of moles of these constant, you just cut their volumes in half." But thats wrong, because you don't cut their volumes in half when diluting, but you cut their concentrations in half.
