Hi there! I figured I had to write a comment. Last year I had my OC exam. I wish I had found your channel earlier than the last days of preperation, but I’m very glad I found it after all. While all your videos I’ve watched have been exeedingly helpful, especially the one on Carboxylic Acid Derivatives stands out to me. It was the last topic of my couse, therefore I didn’t have time to revise it. Thus I had no idea of what was happening in the reactions. I found your 20-minute video on the topic (which is private by now for whatever reason) the afternoon before the exam. It single-handedly made me understand the concept of the reactions of carboxylic acid derivates and I was able to solve 4 of the 5 questions regarding this topic in the exam. Thank you so much for making these simple, yet very informative and helpful videos!
I spent like all morning reading and re-reading text about this and still could not understand it. I am understanding it so much easier now. You, kind sir, are a lifesaver and when I get into vet school, I'll just mail you a copy of my acceptance letter cuz you earned it!
it is so unfortunate as many long video has been removed and only available in premium version, I don't have money and i really2 wanted to watch the long version of the video
At 5:50, why didn’t use the Cl- as the weak base to deprotonate the water since we can reform the carbonyl double bond and have the Cl exit as a leaving group? This way we can see how we get HCl is formed as a byproduct.
Access The Full 42 Minute Video: www.patreon.com/MathScienceTutor
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Hi there!
I figured I had to write a comment.
Last year I had my OC exam. I wish I had found your channel earlier than the last days of preperation, but I’m very glad I found it after all. While all your videos I’ve watched have been exeedingly helpful, especially the one on Carboxylic Acid Derivatives stands out to me. It was the last topic of my couse, therefore I didn’t have time to revise it. Thus I had no idea of what was happening in the reactions. I found your 20-minute video on the topic (which is private by now for whatever reason) the afternoon before the exam. It single-handedly made me understand the concept of the reactions of carboxylic acid derivates and I was able to solve 4 of the 5 questions regarding this topic in the exam.
Thank you so much for making these simple, yet very informative and helpful videos!
I spent like all morning reading and re-reading text about this and still could not understand it. I am understanding it so much easier now. You, kind sir, are a lifesaver and when I get into vet school, I'll just mail you a copy of my acceptance letter cuz you earned it!
I have no idea what this means but ill watch it anyway
I had Ochem two years back. now, I am a CS student, still watching it for no reason at all.
Me when i see zoomer memes
😂
😂
This is perfect timing for me!! We just finished this!!! Awesomeness!!!!☺ Thank you!!!!😃
Nice
it is so unfortunate as many long video has been removed and only available in premium version, I don't have money and i really2 wanted to watch the long version of the video
Which video ⁉️
At 5:50, why didn’t use the Cl- as the weak base to deprotonate the water since we can reform the carbonyl double bond and have the Cl exit as a leaving group? This way we can see how we get HCl is formed as a byproduct.
HCl is a strong acid, having it as a byproduct is not favorable. We only need a catalytic amount of it 🫡
Please drop a video on Dicarboxylic acid
Tysm! This video helped me a lot👍
We gonna focus on 😄😁💜💜
Quick question are you following my syllable great Sir😀
you are really helping me :-) :-)
Can I ask a question? What is this used for?
synthesis of organic compounds
Pharma mostly
I have the 20$ Patreon membership, how can I access the 45 minute video?
Do you use a drawing pad
Ehm... please do u have a trick on how to write a summary well?..
ZEeeeeeeeeeeeereeeeeeeeeeeeeeeeeeeeeeeeeeeeee BESTTTTTT
Hi
❤❤❤
Why you monetized your content
Very bad
wow
Ok
🥺❤️
Plz use white background
Ehm... please do u have a trick on how to write a summary well?..