SN1 Reactions

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Күн бұрын

In this video we'll go over the SN1 reactions, their mechanism, the stereochemistry of the products, and the reaction energy diagram.
00:00 Introduction -- What is SN1?
00:51 Mechanism of SN1
03:36 SN1 Reaction Energy Diagram
04:25 Another Example with Complete Mechanism and the Energy Diagram
07:40 Stereochemistry of SN1 Reactions
10:46 Concluding Thoughts
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Пікірлер: 22

@MadisonSanbower 24 күн бұрын

You single handily brought my OC grade from a 67 to a 91. what a man

@VictortheOrganicChemistryTutor 24 күн бұрын

That's awesome! Keep up the good work!

@me-bf7ip 8 ай бұрын

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!

@curtpiazza1688 10 ай бұрын

Excellent presentation! 🎉

@spurti 2 жыл бұрын

Hii could you make a video on molecular orbital theory???

@anderiabarzanji7354 Жыл бұрын

your videos are very good and explanation is very clear very good videos for exam review (wish me luck and pls make more videos

@VictortheOrganicChemistryTutor Жыл бұрын

Good luck 🍀

@EnglishByORCJA 4 ай бұрын

Why are Tosylate, mesylate and triflate good uncharged leaving groups? Kindly explain , Sir. Thank you, Sir!❤

@CassiusAchilles 11 ай бұрын

Excellent video. Assigning R and S to the products really shows the enantiomeric or diastereomeric products.

@jayakrishna5274 2 жыл бұрын

Sir plz do a video on addition reactions

@VictortheOrganicChemistryTutor 2 жыл бұрын

I'm planning to do a series in the future. I think I should get around those next month.

@narayanupadhyay9181 2 жыл бұрын

Sir can you make video thermodynamics please

@VictortheOrganicChemistryTutor 2 жыл бұрын

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.

@leslievillegas4367 3 ай бұрын

Just to make sure, if our carbocation is sp2 that would be our indicator that the product will result in wedges and dashes?

@VictortheOrganicChemistryTutor 3 ай бұрын

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.

@yasinmuhammad3892 Жыл бұрын

what happens to the hydrogen on the oxygen in the solvent at time stamp at 8.51?

@VictortheOrganicChemistryTutor Жыл бұрын

Nothing. Think carefully what exactly is the nucleophile in this reaction and where it's coming from.

@yasinmuhammad3892 Жыл бұрын

@@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?

@VictortheOrganicChemistryTutor Жыл бұрын

@@yasinmuhammad3892 The nucleophile is the acetate ion of potassium acetate, it's an ionic compound, there's no hydrogen there.

@c_mukhtorova9400 8 ай бұрын

Then what happened to the K in (OK)?

@betul1860 8 ай бұрын

@@c_mukhtorova9400K is spectator ion. It doesnt have an effect on mechanism