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Sn2 reactions | Substitution and elimination reactions | Organic chemistry | Khan Academy
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- Опубликовано: 24 ноя 2013
- Sn2 reactions. Created by Sal Khan.
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Organic Chemistry on Khan Academy: Carbon can form covalent bonds with itself and other elements to create a mind-boggling array of structures. In organic chemistry, we will learn about the reactions chemists use to synthesize crazy carbon based structures, as well as the analytical methods to characterize them. We will also think about how those reactions are occurring on a molecular level with reaction mechanisms. Simply put, organic chemistry is like building with molecular Legos. Let's make some beautiful organic molecules!
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I just don't understand why the lectures in the uni can't explain the concept in simple language. They have to make them confusing to trick the students. Love Khan!
5:50 when i explain to my crush lol
I love organic chem (and I'm a garbage truck driver!!) lol
I hope Khan can help you put your love to practical use. Perhaps you'll merge your knowledge of organic chemistry with your current occupation.
rhoadess
Yes I would certainly hope so, I was thinking about Sn2 reactions on the round today! There is one house that I always get alot of broken glassware to collect, he has a BMW with blacked out windows, he sometimes bungs me a bit of cash, he seems to be doing well in life, maybe I ask him about organic chemistry...
hello man its been 7 years, how you doing now?
@@pomi6320 got a PhD in pharmacology, now work in a research lab!
@@davidsweeney111 so happy for you mate, great how things can take a turn in life! Hope you the best in your upcoming future
There's a garbage truck outside!!!
5:26 I think he wants to say that Br is the leaving group :D
I am pharmacology student and I love the chemistry
This video is amazing
Does the stereo chemistry change?
Quick question: why did Sal draw the C-OH bond on the same side of the Br ion was at? Wouldn't there be steric tension that prevents the OH from entering on the same side of the Br?
shout out to all the 'pairs'
Why are there three videos of this with the SAME example??? All of your SN2 videos (that I've seen, so 3) are where the nucleophile and leaving group are in plane, can we see examples of when the nucleophile and leaving group aren't in plane? Also maybe just see different examples too?
thanks a lott👦
This is an awesome video...
but i couldn't understand the difference between sn1 and sn2 reaction. They seem to be the same. Could anyone please help me understand the difference?
There are many differences, and due to me being lazy, ill give you a couple or more. the first is that SN2's rate equation involves both the nucleophile itself and the the alkylhalide, whereas SN1's rate equation involves only the alkylhalide. SN2 is only one slow step, whereas SN1 occurs in two steps, one fast and one slow. SN2 requires a strong -ve nucleophile, vs the another nucleophile for SN1. Hope this helped even if a little bit.
saif alqahtani Haha don't you think there's a nicer way to say it?
Anyways, you're welcome.
Check out Fred Akins for Organic Chemistry. He's Great!
Feynman blood
I love you
too slow