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Best of luck! Hydroboration is a hard reaction! I've also started weekly "Office Hours" and if you have specific questions, you can always submit them via a form on my website (middle of the home page).
I'm assuming you're referring to the "tricky example" here? They are non-superimposable non-mirror images. If you need the stereodescriptors, we have RR on the left and RS on the right.
@@VictortheOrganicChemistryTutor Thank you!! This means I got it right haha. You have helped me in my ochem 1 class this semester and I am ahead of the curve every time so far (hoping it stays that way.) Thank you for what you do!
plz explain how to identify fronntier orbitals and how to indicate what sort of interaction make sigma and pi bond bond type in it. Sometimes sigma bond is formed through pi type interaction due to ring strains. How to identify ring strain . Plz make video as soon as poossible. I am having mids
I’m not planning on making any in-depth videos on the MO theory this semester. Perhaps, next fall, but I have a lot of other priorities at the moment and the MO theory in organic chemistry is one of the topics that’s not covered in details in a typical course, so it’s not a priority.
actually i m asking it related to organic chemistry point of view , giving touch to frontier orbitals. etc.....but its ok @@VictortheOrganicChemistryTutor
You can support the channel by giving this video a like and leaving a comment below.
You can also make a donation here: www.organicchemistrytutor.com/donate/
Thank you so much for explaining mechanism so clearly that I am not afraid of it anymore!
8 hours before my exam, camping here and i cant believe how i understood everything, thank u 😢❤
Best of luck on the test, fingers crossed 🤞
found you right before my exam thanks victor lets hope this helps
Best of luck!
Hydroboration is a hard reaction! I've also started weekly "Office Hours" and if you have specific questions, you can always submit them via a form on my website (middle of the home page).
Thank you!
You're welcome!
Very helpful. Thank you
You're very welcome :)
For the last example, can you tell me why they're diastereomers? (Can I get the absolute configuration for it just to check myself lol). Thank you!!!
I'm assuming you're referring to the "tricky example" here? They are non-superimposable non-mirror images. If you need the stereodescriptors, we have RR on the left and RS on the right.
@@VictortheOrganicChemistryTutor Thank you!! This means I got it right haha. You have helped me in my ochem 1 class this semester and I am ahead of the curve every time so far (hoping it stays that way.) Thank you for what you do!
plz explain how to identify fronntier orbitals and how to indicate what sort of interaction make sigma and pi bond bond type in it. Sometimes sigma bond is formed through pi type interaction due to ring strains. How to identify ring strain . Plz make video as soon as poossible. I am having mids
I’m not planning on making any in-depth videos on the MO theory this semester. Perhaps, next fall, but I have a lot of other priorities at the moment and the MO theory in organic chemistry is one of the topics that’s not covered in details in a typical course, so it’s not a priority.
actually i m asking it related to organic chemistry point of view , giving touch to frontier orbitals. etc.....but its ok @@VictortheOrganicChemistryTutor
Please !!!!
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