Chemist here, iirc I was taught in uni that triple bonds don't rotate. With that said, since they are linear and don't offer stereoselectivity, a rotation woudnt make the molecule act any different, except maybe its IR spectra.
3:10 can confirm too, I use them everyday too. I have been addicted to taking in atoms since birth! That sounds unhealthy but I promise its not... Though for some reason I can not stop myself from this addiction?
Since the carboxylic acid group is the highest priority, the 'undecanoic acid' part is right, the aldehyde group's carbon (-CHO) is not a part of the longest chain (it is bound to a carbon that is part of the longest chain, -C-CHO), so it will be formyl... The name will be: 8-formyl-5-(hydroxymethyl)undecanoic acid.
I really love your videos! It might not seem that impressive, sometimes, when you explain all the concepts, because they're understood easily. But that's exactly why you're amazing, you explain stuff in such a simple Vsauce way, step by step, so that basically anyone can understand complex stuff by the end of the video. I wish you the best of luck, and also, how in the hell do you make videos like this in such a short time? Like, I can get the animations, but all the investigation?? It's crazyy!
I did end up asking a couple other chem people about the triple bond thing and the general consensus is that it doesn't rotate - I think the donut thing was from a specific context (spectroscopy) where you're assuming delocalised electron density because the entire bond rotates freely
My brother in humanity, Try to learn morphing animations it will help your videos have a flowy feeling instead of static and harsh experience, and i appreciate your love and enthusiasm for Knowledge and Understanding. Keep it up ❤
Man, I love being a liberal arts major. Mostly philosophy courses. Weirdly enough, I love chemistry (and o-chem) a lot. Guess I am really messed up in the head, huh?
I want an explanation how he got "2-methal-butyronitrile" lol, students taking organic for the first time don't mess that up... Anyway, thank you for catching that, I must've missed it skipping forward.
I was wondering if the molecule you numbered was correct, but i can't seem to find sources for your friend's naming of said molecule. I am not that well-versed in organic chemistry, but i have some questions. I'm sure this is just an editing mistake, but you kept saying decanoic acid instead of undecanoic acid, which was shown on screen. Secondly, from what i could find, a ketone group is indicated by just "oxo"; no need for methyloxo. When naming the methyl substituent with a hydroxyl group, it should actually be hydroxymethyl, not methylhydroxy, even though i have seen it in simplified versions of IUPAC names. I'm pretty sure this isn't standard IUPAC naming, but as I said, I am not that knowledgeable on the subject.
Oh no not the chemistry interpretation of orbitals and atoms not have function oh no that doesnt seem right to me i mean physics is better wht this long nami g convention just add subscrpits like physics does when you need to name something
Waiting for that chemist who’ll confirm whether double Pi bonds can or can’t rotate…
Let me know when you find out
@ Oh I will
Why are you using "Double" and "π" at the same time? Double bonds already include π bonds.
@@LmaoDed-hahaDouble π bonds, not double bonds. Though I can see why that’s confusing, however it’s what MAKiT called them so I went with it lol.
Chemist here, iirc I was taught in uni that triple bonds don't rotate. With that said, since they are linear and don't offer stereoselectivity, a rotation woudnt make the molecule act any different, except maybe its IR spectra.
That is the biggest issue, because the three kinds of sources I was able to find were:
1. They do rotate
2. They don't rotate
3. It doesn't matter
Crazed man's rambling finally came to fruition
I’m taking AP chem this year and ur videos carried me through the quantum mechanics bit
3:10 can confirm too, I use them everyday too. I have been addicted to taking in atoms since birth! That sounds unhealthy but I promise its not... Though for some reason I can not stop myself from this addiction?
WRONG MAKIT! I clicked because the thumbnail was indeed interesting.
Since the carboxylic acid group is the highest priority, the 'undecanoic acid' part is right, the aldehyde group's carbon (-CHO) is not a part of the longest chain (it is bound to a carbon that is part of the longest chain, -C-CHO), so it will be formyl... The name will be: 8-formyl-5-(hydroxymethyl)undecanoic acid.
Just what i was searching for 👍
How you made a video in a week?
Desperation and complete lack of sanity
@@MAKiTHappen dudes its insane to me because usually with animations like this youtubers would take like 3 months at least
@@MAKiTHappen😅after seeing the server i can understand😂
voodoo magic
I don't know how you're explaining it better than when I was learning chemistry in highschool
"when I showed it to someone who knows a thing or two about organic chemistry" you mean Dr Flaym?
Flaym was busy becomming a literal dr, it was pharmamane
I really love your videos! It might not seem that impressive, sometimes, when you explain all the concepts, because they're understood easily. But that's exactly why you're amazing, you explain stuff in such a simple Vsauce way, step by step, so that basically anyone can understand complex stuff by the end of the video. I wish you the best of luck, and also, how in the hell do you make videos like this in such a short time? Like, I can get the animations, but all the investigation??
It's crazyy!
I don't quite know what to say, thank you so much for this comment I really appreciate it
The reason I clocked on this video because it's a MAKiT video.
clocked
I'm actually currently learning organic chemistry in school and I can confirm it's significantly more fun than electrochemistry.
Ah yes , my third Abitur Subject
Your animation is so amazing and your talking stylish so amazing and iconic bro
And he delivers again. Great work makit
I did end up asking a couple other chem people about the triple bond thing and the general consensus is that it doesn't rotate - I think the donut thing was from a specific context (spectroscopy) where you're assuming delocalised electron density because the entire bond rotates freely
Chemistry time
THANK YOU THANK YOU MAN🙏 you are single handedly going to save me from my finals
My brother in humanity, Try to learn morphing animations it will help your videos have a flowy feeling instead of static and harsh experience, and i appreciate your love and enthusiasm for Knowledge and Understanding.
Keep it up ❤
Man, I love being a liberal arts major. Mostly philosophy courses. Weirdly enough, I love chemistry (and o-chem) a lot. Guess I am really messed up in the head, huh?
gimme that epic science content daddyMAKiT
YAY ANOTHER MAKiT VIDEO YEAAAAAAAAAAH!
Organic chemistry my beloved
Great Video.
Fact
Makit, i think you're losing sanity from studying chemistry..
Honestly, relatable :]
Toughness.. i saw that beautiful word in your charity checkup the other day
As it is rules since I follow, I see MAKiT upload, I click and then I am gonna get confused and fascinated at the same time.
Great visuals
12:44 you messed up. The group is popping up way after THIS is said.
This is like a one shot speed up to 2x, a good ride if you know the concepts he talks abt,
That was a phenolmenal joke 😂😂😂
Alright fine, I’ll join your patreon.
16:19 The IUPAC name should be 2-formylbutanenitrile
I want an explanation how he got "2-methal-butyronitrile" lol, students taking organic for the first time don't mess that up... Anyway, thank you for catching that, I must've missed it skipping forward.
Chemistry, the study of exeptions
I think that if you add Nomenclature somewhere in the title, you can get a lot more views from students looking it up!
1:43 dude I didn't expect Makit with a long arm wtf
I found the thumbnail interesting!
Makit is cookin with the vids
I was wondering if the molecule you numbered was correct, but i can't seem to find sources for your friend's naming of said molecule. I am not that well-versed in organic chemistry, but i have some questions. I'm sure this is just an editing mistake, but you kept saying decanoic acid instead of undecanoic acid, which was shown on screen. Secondly, from what i could find, a ketone group is indicated by just "oxo"; no need for methyloxo. When naming the methyl substituent with a hydroxyl group, it should actually be hydroxymethyl, not methylhydroxy, even though i have seen it in simplified versions of IUPAC names. I'm pretty sure this isn't standard IUPAC naming, but as I said, I am not that knowledgeable on the subject.
oh hey, makit did it in time
Yo its so late why cant i be in a different time zone, I should be asleep and ready for school
Same
Who needs sleep when you have Makit
i like your funny words magic man
You deserve more
a casual nine year old watching stuff that is for university students
Time to learn chemistry ig
Keep going🎉🎉🎉
I WAS IN THE VIDEO MOM GET THE CAMERA
I still cant get over "sigma" being a thing used well before the meme yet it still making me laugh
Thoughness.
The lack of music in the chains section is off putting lol
Oh no not the chemistry interpretation of orbitals and atoms not have function oh no that doesnt seem right to me i mean physics is better wht this long nami g convention just add subscrpits like physics does when you need to name something
what is happening...
Wish you had more reach 😔
W vid
cool, thanks!
First hour gang where u at
4h ago
That intro music is now synonymous to your videos now ong
Makit, i think you're losing sanity from studying chemistry..
Honestly, relatable :]