To anyone who hasn’t studied Organic Chemistry a bit, forewarning it’ll be bad at first, but it will get better. Mostly I mean reaction mechanisms here but in general. You’ll feel more satisfied and more motivated the more you go on.
You guys, seriously, LIVE SAVIOURS. My organic chemistry course is starting next week. Can you imagine my sheer relief at seeing this course on ur channel? Thanks!
omg you're such a good teacher. I've already had all my org chem classes and I still don't understand a lot of the basic stuff. My teachers actually didn't bother to teach us this :/
Thank you for the video. Have you ever considered creating a course oriented more towards mathematics? I am an avid fan of your videos, but often have to turn to other resources for mathematical help.
Math is definitely a tricky one for us. We've made a couple attempts - Statistics here on this channel & this summer we did Alegbra with ASU. But who knows, maybe down the line we'll try other math coures! -NS
I have a question: According to the reaction mechanism isn’t the reverse reaction also possible for all reactions Take benzyl chloride for example. We can draw a reaction mechanism for the given reaction C6H5CH2Cl + H2O = C6H5CH2OH + HCl But we can also do the same for the reverse reaction which is not possible in real life. So how do we know if the given reaction mechanism will actually happen?
When it comes to pee production, whales are world champs. A single fin whale is thought to produce around 1,000 liters (260 gallons) of urine each day - enough to fill a 10-by-6-foot kiddie pool.
@@Hambxne and i would like to add ... And all the water they get is from their food they can't drink sea water So it means if they starve they also are dehydrated Edit: some species of whales will not eat seasonally , they get the water from their fat stores/blubber When you burn fat you get energy Which gets converted to heat , co² , and water .
The acetylide salt + cyclohexanol reaction is probably occurring in aqueous solution, otherwise the salt wouldn't dissociate, right? So why doesn't the acetylide ion attack the protons in the H2O molecules instead? Is it because the carbonyl's δ+ carbon atom is somehow more electrophilic than the hydrogen atoms in the water? The bonds in water have an electronegativity difference of ~1.2, and the carbonyl double-bond has an electronegativity difference of ~1. So why is it that, in this reaction, water's protons are less attractive to the acetylide ions than the electrophilic carbon in cyclohexanone?
I understand that water is formally excluded from the first step in the reaction & that this is just a pedagogical proof of concept, but in a real situation, how would I be able to *predict* that the acetylide would attack the δ+ carbon atom instead of one of the *more* δ+ protons in H2O?
ok I just read on Wikipedia that the reaction is usually done in liquid ammonia, which is a nucleophile & so would not be attacked by the acetylide. I guess I answered my own question lol.
11:45 I loved the phrase "Don't panic" that makes me remember the cover of Hitchhiker guide to the galaxy book. Like if you read that awesome book. Nice content. Leave my like.
To the person that’s reading this: You’re very intelligent and adorable human! Stay healthy during quarantine My Dream is to have 70k. I been struggling to get there💚
A few misleading things in this video. First of all a lot of the structures are not great: molecular geometries were wrong for sulfuric acid and H3O+, and there’s the tendency to show square-planar-type structures for organic molecules - obviously people do this for the purpose of teaching, but then when you want to show a mechanism, e.g. an elimination, you need to introduce another method of representation for it to make sense. Speaking of which, the reversible hydration/dehydration would surely give the E alkene as the major alkene component, very quickly. As presented in the video, it makes it look like you would have a mixture of the Z alkene and the alcohol, which effectively would not be true. Also the reference to pKa was quite odd: why state that the protonated alcohol has a low pKa if it’s not going to be compared to H3O+ in the forward direction?
![Noob To Max With DRAGON REWORK In Blox Fruits [FULL MOVIE]](http://i.ytimg.com/vi/LnBMOinoOvA/mqdefault.jpg)
Production values are exceptional. Huge respect to your awesome animators
Aw thank you! This made me smile :)
To anyone who hasn’t studied Organic Chemistry a bit, forewarning it’ll be bad at first, but it will get better. Mostly I mean reaction mechanisms here but in general. You’ll feel more satisfied and more motivated the more you go on.
this is where o-chem all went downhill for me 🥴
You guys, seriously, LIVE SAVIOURS. My organic chemistry course is starting next week. Can you imagine my sheer relief at seeing this course on ur channel? Thanks!
omg you're such a good teacher. I've already had all my org chem classes and I still don't understand a lot of the basic stuff. My teachers actually didn't bother to teach us this :/
So, so grateful for the people at Crash Course.
I lost track of what's happening 10 episodes ago. This isn't even my major. I don't know why I'm still watching 😂
Well this is major and i lost track too 😂
This channel is a savior when
It comes to reviewing for my exams.
I just can't take my eyes off of the background colors matching in yellow.. 😂
FINALLY, I GET IT
thank you ever so much that was a wonderful and clear explanation, and the visuals really helped
i love mechanisms , its so logical and fun
You are AMAZING! I'm taking Ochem 2 and this is such a helpful refresher for the small details
Just in time for my quiz later. Thank you.
Thank you for the video. Have you ever considered creating a course oriented more towards mathematics? I am an avid fan of your videos, but often have to turn to other resources for mathematical help.
Math is definitely a tricky one for us. We've made a couple attempts - Statistics here on this channel & this summer we did Alegbra with ASU. But who knows, maybe down the line we'll try other math coures!
-NS
I wonder what the mechanism is for "Turn the O2 into the O3, dawg".
Google the Chapman cycle!
Great teacher ❤
This is such an excellent educational tool.
It would be so great if after this classes we had some exercises...
If you download the app they have some "notecards" that I've actually found very helpful.
I have a question:
According to the reaction mechanism isn’t the reverse reaction also possible for all reactions
Take benzyl chloride for example. We can draw a reaction mechanism for the given reaction
C6H5CH2Cl + H2O = C6H5CH2OH + HCl
But we can also do the same for the reverse reaction which is not possible in real life.
So how do we know if the given reaction mechanism will actually happen?
Why doesn't the HSO4 negative charge attack the carbocation more readily than the water? Steric hinderance?
Random fact:
Blue whale tongues can weigh as much as an elephant.
When it comes to pee production, whales are world champs. A single fin whale is thought to produce around 1,000 liters (260 gallons) of urine each day - enough to fill a 10-by-6-foot kiddie pool.
@@Hambxne and i would like to add ...
And all the water they get is from their food they can't drink sea water
So it means if they starve they also are dehydrated
Edit: some species of whales will not eat seasonally , they get the water from their fat stores/blubber
When you burn fat you get energy
Which gets converted to heat , co² , and water .
Wow 🤩😲very informative video!!!!
Thanks now I get it
I got most of it but what happened to the HSO4? Why was it not added to the reaction
i love you crash course💚
Thanks for uploading new video.
just in time for my orgchem quiz this friday
Thank you Crash Course, you give me something new in this video. XD
Nice piece.
Great explanation of Reaction Mechanisms.
@@FlamingBasketballClub We publish short documentary-style films usually 3-minutes or less Monday - Friday!
The acetylide salt + cyclohexanol reaction is probably occurring in aqueous solution, otherwise the salt wouldn't dissociate, right? So why doesn't the acetylide ion attack the protons in the H2O molecules instead? Is it because the carbonyl's δ+ carbon atom is somehow more electrophilic than the hydrogen atoms in the water? The bonds in water have an electronegativity difference of ~1.2, and the carbonyl double-bond has an electronegativity difference of ~1. So why is it that, in this reaction, water's protons are less attractive to the acetylide ions than the electrophilic carbon in cyclohexanone?
I understand that water is formally excluded from the first step in the reaction & that this is just a pedagogical proof of concept, but in a real situation, how would I be able to *predict* that the acetylide would attack the δ+ carbon atom instead of one of the *more* δ+ protons in H2O?
ok I just read on Wikipedia that the reaction is usually done in liquid ammonia, which is a nucleophile & so would not be attacked by the acetylide. I guess I answered my own question lol.
Thanks so much
Really like arrow pushing!
11:45 I loved the phrase "Don't panic" that makes me remember the cover of Hitchhiker guide to the galaxy book. Like if you read that awesome book. Nice content. Leave my like.
To the person that’s reading this:
You’re very intelligent and adorable human!
Stay healthy during quarantine
My Dream is to have 70k. I been struggling to get there💚
why is water still floating? i’ve never been able to grasp why it is still there
I really love organic a lot😘🥰😍
Hey are u from India? I'm from India! Love u guys!
A few misleading things in this video. First of all a lot of the structures are not great: molecular geometries were wrong for sulfuric acid and H3O+, and there’s the tendency to show square-planar-type structures for organic molecules - obviously people do this for the purpose of teaching, but then when you want to show a mechanism, e.g. an elimination, you need to introduce another method of representation for it to make sense. Speaking of which, the reversible hydration/dehydration would surely give the E alkene as the major alkene component, very quickly. As presented in the video, it makes it look like you would have a mixture of the Z alkene and the alcohol, which effectively would not be true. Also the reference to pKa was quite odd: why state that the protonated alcohol has a low pKa if it’s not going to be compared to H3O+ in the forward direction?
“The mind is not a vessel to be filled, but a fire to be kindled.”
― Plutarch
Ah, the things nightmares are made of
When can we expect more episodes?
why do you input an empty line before every line of your subtitles?
Corona:"I spread fast"
Me: "not faster than crash course views"😎
Mmmm, no there are many other channels get more views in less time
@@prem5176 yup
Wish I had this for orgo 1. I barely passed with a B but im stuck in orgo 2
Thanks
“Who else is reading comments and not watching in full screen?😂”
*(Hey CrashCourse thanks for commenting on my new video)❤️*
hello
Ikiooo[z,fromdwaaAaronaoll0cx.ca4y
I can't stop hearing her name again and again. Nice name.
I wish I found this channel sooner
Excellent presentation, thanks.
That warning sign was scary
They use my own professor's book for the videos so this really works for my class
Ohhhhhhhhhhhhh !!!!! 16th comment I love CrashCourse.
Soooo gooood! Can you show us elimination of N2 form amines (by HNO2) . I thinks that it s very interesting reaction. Good luck
cant understand a thing 😭😭
"Be less curious about people and more curious about ideas."
-- Marie Curie
Organic Chemistry explained by Marvel:
Chemistry: Nucleophilic War
Chemistry: Endgame
Idk if I’ve ever been this early
“Wonder is the seed of knowledge”
― Francis Bacon
Just stop...it's more like spamming now
Most people driving don't seem to know what a Yield sign means.
Yay, app!
can i get a shout out?
Diversity!!!! In your hosts we love to see it!!!
I hate school
in the next video,deboki di plz try to explain the diff. btw inductive ,electromeric,mesomeric n hyperconjugation....really it ll help me a lot...🙏
When will crash course Asian and African history come.
Wait
she looks like camilla cabello
👍👍👍👍👍👍👍👍👍👍
Hot Mic.
So, to the business of business.
I am an unreactive mechanism
Me watching their videos from 2013...
Organic reactions tend to proceed to give multiple products. Usually one of.the products is a polymeric material often called tar.
When did science look so damn good 🤤
When your organic chem teacher doesn't teach you properly!
27 seconds gang
Way over my simple mind.
I thought I was going to finally learn how to drive uggg...
Oy
You lost me at electrophilic additions of a protein to an alkaline.
I need to go back over my high school chemistry lol
Early birds post the first comments
Dope
Almost First
Can you guys please bring back Human Geography T_T
So tired of reaction videos.
The real life map analogy is so unnecessary. Can’t we just get to the point?
Sorry, you are what?
Focus on the problem rather focusing on theories in organic chemistry .we need much practice to familiar with OC.