Organic Chemistry - Video Lessons: www.video-tutor.net/organic-chemistry.html Access The Full 33 Minute Video: www.patreon.com/MathScienceTutor Direct Link to The Full Video: bit.ly/3yhQfS4
@@conquesotador Thanks, and I hope orgo starts going better! If you ever want to hear a pun, just reply to one of my comments (or leave a comment on one of my videos) with a specific topic. For instance, had you said “carbonyl”, I might have asked: A: What type of slender fish can make four bonds? A: A carbon-eel.
Iss the six membered ring substrate more reactive than the five membered ring diene in the Diels-Alder Reaction? BTW love your videos. Thank you for your efforts. It is much appreciated!!
Im curious to know, will the endo products always be the major products? I would figure the -COOH would be more stable in an equatorial position rather than an axial position due to the energy penalties. Or am I seeing it wrong?
Do your curved arrows always have to be in the counterclockwise direction? Naturally, I want to draw the arrows in the clockwise position and I think it would yield the same product but I just want to be sure.
9:39 why is the endo product the major product? This seems counterintuitive. Would there not be more strain when the CHO group is next to the longer bridge?
It's a bit dramaticaly drawn, it should be a normal tetrahedral angel. Becuase the -COH Group is relatively big, it is favourable to have it as far away from other Groups as possible. I hope it is obvious from the pictures that the endo Postition is stericaly much more favourable. Edit: This would be the Exo form: pasteboard.co/JI8id5B.jpg This would be the Endo form: pasteboard.co/JI8iHa2.jpg
His name is Julio Gonzalez. Considering he did a B.A. from UCLA, and is a staff member at Dept. of Biochem there, and has been uploading videos since 2015, I guess his age would be 25-35 in any case.
Organic Chemistry - Video Lessons: www.video-tutor.net/organic-chemistry.html
Access The Full 33 Minute Video: www.patreon.com/MathScienceTutor
Direct Link to The Full Video: bit.ly/3yhQfS4
Diene? More like dying, for more of this high-quality content! Thanks so much for making *so much* of it and then sharing.
Take my upvote and make some more puns pls im dying in orgo
@@conquesotador Thanks, and I hope orgo starts going better! If you ever want to hear a pun, just reply to one of my comments (or leave a comment on one of my videos) with a specific topic. For instance, had you said “carbonyl”, I might have asked:
A: What type of slender fish can make four bonds?
A: A carbon-eel.
@@PunmasterSTP Ok let me make this hard, Pthalimide!
@@ronin4923 I could make a lame pun about it, but I'm sure that would just be a source of a-moan-ia.
@@PunmasterSTP LOL made my day (night actually)
If I could, I'd pay my tuition fees to you, cause youre the real prof!!!
By now, I've come to expect brilliance from you, but I still can't help being baffled by how good you are at simplifying these topics.
You were literally my chemistry lecture😩🙏thank you so much..from Africa(Zambia)
i didnt know africa had organic chmistry lol
@@gartyqam no ur right there are no univerities in africa only mud huts...🤣
How does anyone go about making 2,491 videos from two minutes to an hour in length? It's amazing.
Passion, and a love for teaching.
For which I am so god damn thankful.
I've skipped class this whole semester and only watched your videos. Thanks for being the professor that my professor couldn't be:)
How’d you do?
Yeah, how did it end up going?
@Name lol fr
Felt this lol
Honestly thank you so much for these videos they make these concepts so much easier to understand, you're the ochem goat
Thank you bud ❤
my guy knows literally everything and he deserves the best in this world 🎉
Youre the lifesaver for me for 3 years
Your amazing!!! Every video watch, you make chemistry so easy to under stand. Thank you
he single-handedly saved my grade
was having a hard time getting the mechanism , thanks for the trick
Thank you so much for your contents and help!
can you bring a video about how to find relative molecular mass
Yah please bring
omg u came back!!! ily❤️
Are you a professor? You should be a professor, your amazing!
Thanks for this video! You save my life😭😭
You are the best!! 💫
this video is very informative for me thank you sir
Omg you’re the best
adore this channel!
THANK YOU SO MUCH! UR REALLY A LIFE SAVER!
thank you so much
Thank you so much .....
cry in happiness! Yes endo rule over the the exo. Point it down!
You think you can make linear algebra videos? Thank you for all you do!
This was such a godsend
excellent explanation
Awesome sir
you are first congrats!!!!
SIKE
You're really cool I am very grateful to you❤️🐞
Can u please do videos about reflection over y=mx and y=mx+b? thank you for all you do
thanks bro it helps a lot
Thank you hero 🙏
Thanks you
Sir you are a Genius can we see your face ...
Iss the six membered ring substrate more reactive than the five membered ring diene in the Diels-Alder Reaction?
BTW love your videos. Thank you for your efforts. It is much appreciated!!
Why is the endo position more favourable??
Im curious to know, will the endo products always be the major products? I would figure the -COOH would be more stable in an equatorial position rather than an axial position due to the energy penalties. Or am I seeing it wrong?
yo mama
@@annieharmer1636 ur a loser
Thank you very much sir
REALLY GOOD!
Is the endo product major due to steric hindrance?
hey thanks
thank you man💞
thank you so much!
Why you won't mention the example of 2,3-dimethyl butadiene and butenone😒😒😒🥺🥺
Thanks🤗
Do your curved arrows always have to be in the counterclockwise direction? Naturally, I want to draw the arrows in the clockwise position and I think it would yield the same product but I just want to be sure.
The only rules with curved arrows is that it has to go from negative charge to positive charge
Hi JG, are the first and second answers missing double bonds? Thanks
I'm pretty sure you're right. A pi bond is being formed.
@@slothgoth7134 yeah. i have an exam tomorrow so hopefully we're right! thank you!
can you tutoring of how the reaction to produce cyclohexyl chalcone derivative?
Top notch...!!
Missed you
In the trans example these two products are identical
thank u so muchhh
I've seen this topic be longer in duration, is it deleted?
It seems like he is putting his full length videos on patreon.
@@peybak its a free?
@@erwinaditya9824 no
Can u use red instead of blue?
9:39 why is the endo product the major product? This seems counterintuitive. Would there not be more strain when the CHO group is next to the longer bridge?
It's a bit dramaticaly drawn, it should be a normal tetrahedral angel.
Becuase the -COH Group is relatively big, it is favourable to have it as far away from other Groups as possible. I hope it is obvious from the pictures that the endo Postition is stericaly much more favourable.
Edit:
This would be the Exo form: pasteboard.co/JI8id5B.jpg
This would be the Endo form: pasteboard.co/JI8iHa2.jpg
@@kaikabuth7558 I see it now, the bigger ring actually gives more space despite having more atoms, thank you!
Here with 27 likes 👍
Serious question does anyone know how old he is
He's 102.
He’s pi
Maybe in 20's
His name is Julio Gonzalez. Considering he did a B.A. from UCLA, and is a staff member at Dept. of Biochem there, and has been uploading videos since 2015, I guess his age would be 25-35 in any case.
@@shishirmaharana4022 how come u know that?
Also tell the IUPAC names
What's endo and exo ?
Wonderfully
Is this reaction taught in orgo 2?
@@malcolmcollins4732 Thanks man
Chemistry god
*still here*
YES
Don’t mind that k just wanted to be first
My professor or the book didn’t tell us to draw that the bicycle that way. Thank you so much. This is easy now 💯💯😭😭🫡🫡🫡
so confused why the shape suddenly changed....
It doesn't matter.
I hope it's not too late 😭
@@monicamuchimba3973 lol in the long run it didn't matter 😂 I'm a pharmacist now that doesn't even remember this reaction
@@roo8258 in that case congratulations 🎉🤣🤣
@@monicamuchimba3973 thank you 😂
Noticeee meee pleaseee😱😵🥰
Thank you, my professor is useless.
thxxxxxxxxx :)
Wow
GG YOU FIRST
@@AbdullahKhan-nq9gj yup
for anyone watching
don't draw your arrows like he does
you will probably lose points if your professor is anything like mine
Alder is my name
First
your third
i meant 2nd
No, first, sort by newest first and scroll to the bottom.
EARLY!
Firstt
your 5th
your 5th
Thank you so much 🙌
Thank you so much!!
First
your 4th
i meant third