These videos are excellent, what a lot of other chemistry channels lack is the small details so I always had questions on those, but you managed to answer all of them. Thank you so much!
With the exception of vinylic carbocations, they all are sp2 hybridized. It's not an "if" statement. And whenever we have a reaction that has a carbocation as an intermediate, you're *always* going to have some degree of racemization in your product. In most cases, we're going to get ~50/50% mixture of both possible stereoisomers.
I am going to be adding some aspects of thermodynamics when it's applicable towards the concepts I'm discussing, but I'm currently not planning any non-organic chemistry related videos in the near future.
@@VictortheOrganicChemistryTutor the oxygen portion I would think. But I guess what I'm asking is, did you exclude the H from that part of the drawing for a particular reason?
These videos are excellent, what a lot of other chemistry channels lack is the small details so I always had questions on those, but you managed to answer all of them. Thank you so much!
Agree
You single handily brought my OC grade from a 67 to a 91. what a man
That's awesome! Keep up the good work!
thank you victor for your best teaching. pray me to succeed in my senior exam😊❤
Best of luck!
Excellent presentation! 🎉
your videos are very good and explanation is very clear very good videos for exam review (wish me luck and pls make more videos
Good luck 🍀
Excellent video. Assigning R and S to the products really shows the enantiomeric or diastereomeric products.
Why are Tosylate, mesylate and triflate good uncharged leaving groups? Kindly explain , Sir. Thank you, Sir!❤
Just to make sure, if our carbocation is sp2 that would be our indicator that the product will result in wedges and dashes?
With the exception of vinylic carbocations, they all are sp2 hybridized. It's not an "if" statement. And whenever we have a reaction that has a carbocation as an intermediate, you're *always* going to have some degree of racemization in your product. In most cases, we're going to get ~50/50% mixture of both possible stereoisomers.
Hii could you make a video on molecular orbital theory???
Sir can you make video thermodynamics please
I am going to be adding some aspects of thermodynamics when it's applicable towards the concepts I'm discussing, but I'm currently not planning any non-organic chemistry related videos in the near future.
Sir plz do a video on addition reactions
I'm planning to do a series in the future. I think I should get around those next month.
what happens to the hydrogen on the oxygen in the solvent at time stamp at 8.51?
Nothing. Think carefully what exactly is the nucleophile in this reaction and where it's coming from.
@@VictortheOrganicChemistryTutor the oxygen portion I would think. But I guess what I'm asking is, did you exclude the H from that part of the drawing for a particular reason?
@@yasinmuhammad3892 The nucleophile is the acetate ion of potassium acetate, it's an ionic compound, there's no hydrogen there.
Then what happened to the K in (OK)?
@@c_mukhtorova9400K is spectator ion. It doesnt have an effect on mechanism
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