My name is Joe Del Nano, and I created jOeCHEM joechem.io. I made jOeCHEM--my own guide through Organic Chemistry I and II--to help others learn the subject. There are videos for all topics with guided worksheets + solutions ALL FOR FREE.
Here on my KZread channel are all the video tutorials, and I've also organized the videos into playlists that mirror where they would typically fall into chapters in a given Organic Chemistry textbook. In the description of each video are links to my website, where all the guided worksheets + solutions are linked for each and every video.
I'm a firm believer that anyone can excel not only at Organic Chemistry, but any subject with a consistent focused effort. But no one achieves anything alone. I'm here to help you in your carbon conquest every step of the way.
So if you're new to jOeCHEM and looking to conquer carbon based chemistry, join the team. Let's go from Lewis Structures to DNA & Peptides and show Organic Chemistry who's boss.
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Thnx
U gained one subieess MAN!!!😭😭😭😭😭😭
Nice one
Teaching was good Thank you
Hint: When you draw an alpha you go down with your pen (so if its alpha the OH on the first C will go up) and for beta your pen will go up by writing the letter ☺ thank me later THIS WILL ONLY WORK FOR D SUGARS
Wow! I was kinda confused about this. THE EXPLENATION WAS AMAZING!!! BINGO BANGO BONGO I GOT IT NOW 😭😍
In class I've heard a saying that helped me memorize: HAAKTEAM (H - halogens, A - Anhydrides, A - Aldehydes, K - Ketons, T - Thioesters, E - Esters, A- Amids, M - Carboxylic acids. The last letter is kind of useless, but it helped me to know im missing one more)
Great video! Thank you Joe
thank you so much
i want to be in this guys gang
well explained, thank you! now I finally know how the first step of the Corey-Seebach reaction works
at 4:49, you said there was hydrogen, but is it not a carbon? or I guess methyl group?
ngl when i first saw this in our lecture notes, my first impression was also "what the hell is this" 🤣
you re making this so much easy for uss. You re the bestt!!!
You are the best!😅
such a great video, nobody else explained it this clear
great work!!!!!!!
The same explanation as they did in Breaking Bad. I won't ever forget about chirality now.
literally saved my life, thank you!!
Thank you for helping me understand the witting reaction
you are amazing gang
i love you gang thank you so much, you explained what my professor couldn't
THANK YOU SO MUCH!! I was very confused about this topic in my textbook and in lecture, and you made it so straightforward and simple.
Great job
Niceee explanation
saw this terminology everywhere without knowing what it means. thanks for explaining this, you saved me a lot of headache!
I hope to see you too Best Ochem teacher ever ecisted
Thank you for your efforts, and thank you for the translation into Arabic.
بارك الله فيك ❤️
We had studied this in pharmacy college
I was struggling so hard trying to understand this in my classes. Thank you so much for your easy explanation 🥲❤
THANK YOU SO MUCH JOEE
Thanks so much you are really wonder full Man! Keep it up with your profession l love you! highly educated teacher l hope you will solve my any academic problem
Thanksss
thank you for the clear explanation!!!
Thanks fr 🙏
Thanks brother ❤
Senin gözünün yağını yiyim ellerine ağzına diline sağlık dostum
Thank youu
thank you soooo much man, you're good at what you're doing, please keep posting videos !!!
But how do we know how the enol will be formed?
How would a cyklohexylbutanal react with KMnO4?
Thank you from Korea 🥳
keep going bro great explanation 😇
Thank you so much! Your explanation was so much better to understand.
I LOVE YOU
you are great thank you😍😍😍😍😍😍
Thank you soomuch ❤
absolute legend thank you jOeCHEM
4:15 Why couldn't an intramolecular step occur where the OH abstracts a proton from the positively charged oxygen? Is it because we're in an acidic environment which makes it more energetically favourable for it to abstract from H30+ instead?