Organic Chemistry PDF Worksheets: www.video-tutor.net/orgo-chem.html Full-Length Exams & PDF Worksheets: www.patreon.com/MathScienceTutor/collections Direct Link to The Full Video: bit.ly/3itPNy2
Thanks for all of your videos. You are the reason I got an A in my organic chemistry course. You explain things better than my college professor who is the head of the chemistry department! Way to go!
This is actually more useful than my professor at uni!!! You explained it so well and made it so much more understandable. Thank you so much for saving me hours of going through my lecture notes!!!
i want to say i love you so much for all your videos. I have a terrible professor this semester for organic chem and was struggling until i found your videos. thank you so much.
Converting it to a lewis dot (i think that's what that is) before diving straight into the newman makes it SO SO SO much easier for my brain to see! Thank you so much for that method, it's foolproof for me!!! I never would have gotten it without that trick because I have trouble visualizing things. THANK YOU!!!!
Properly explained! Really enjoyed it 😀 We could also make Saw-Horse Projections and just condense it's structure by joining the front and back Carbon atoms to get Newman's!
@@pauludom you are looking it from a different perspective. If anyone wants to learn properly he/she will have to study it correctly to understand.otherwise there will be a confusion. Think it that way.
Can you please do more videos about H-NMR spectroscopy and C-NMR spectroscopy as well as gas and HLPC chromatography, I really need some exercises and questions about these topics as soon as possible because I am not able to find some unfortunately
In Which class does your teacher or professor teach this topic in your nation??? In India, In competitive approach it's Highschool 1st year i.e. class 11th Topic. . Thank you for wonderful explanation 😊.
It's simple. All you have to know is this law is only applied in symmetry questions like cylinrcal or spherical symmetries. It's much easier than coulomb's law.
i feel that is so saddening that i have to come to youtube to learn material thats gone over in class rather than actually learning the material in class
21:07 Why is comformation at the right corner more stable than the one at the left corner if they both have one gauche? How do I determine which one is the most stable of the two? I know that the most stable must be the one with the lowest potential energy but don't the two of them have the same potential energy? Or am I wrong? Do I have to do some steps to solve it? D:
I didn't get you, did he said that the right one is more stable than the left one? 20:58 he said, both the conformations are actually same with same potential energy, so you can choose either of them as they both are same but not the middle one
It's a shame that dislikes are no longer publicly visible, as that would've shown that this is an actually usefull and great explanation of the exact subject matter in a world of bad, slow, subject-irrelevant or otherwise lacking tutorials.
Hi, Any ideas for 18:12? My guess (without doing too much research yet) is that molecule 3 is the highest in energy relative to the other 2, given the numbers. Would you say that’s right, or do you suggest I do more research? Thanks, Rina
is it not possible to put an ethyl group directly behind a methyl group on the top? 16:30 cuz then there'd be another solution. And I'm also confused if a methyl and ethyl group can change their order just like this ... ? one time, the methyl group is on the right side of the ethyl group, the other time it's on the left side. The substituents should just rotate, not change their places, or is it agreeable? I would be glad if someone could explain!
How are low energy confirmations calculated, and if it can be done by hand, why can’t people find low confirmations of low energy of complex molecules? I understand it’s a calculation problem, but why is it hard to know what the low energy confirmations are with more complex molecules? Is it a random sample, and you just have to go through each confirmation to determine it’s angle and energy level?
Why is it near impossible to just determine only the finite number of low energy confirmations for complex molecules? And does the angle determine the energy level, or is the angle considered, but it’s matters where each atom is in Three-dimensional space?
