Lol, the pause at 21:51 was funny. Reminds me that even Chad has to stop and format his thoughts. Thank you so much for the videos Chad!
@ChadsPrep2 жыл бұрын
You're welcome - glad you enjoy them!
@sharkbait99224 күн бұрын
Chad always saving the day
@ChadsPrep4 күн бұрын
Thanks!
@26d83 жыл бұрын
This a great video on this topic, covered all the reactions. Thank you so much.
@ChadsPrep3 жыл бұрын
Glad you enjoyed it, Samira!
@SonFather-x1r14 күн бұрын
Nice work Keep it up God bless you
@ChadsPrep13 күн бұрын
Thank you - to you also!
@ranamohamed1196 Жыл бұрын
شكرآ جزيلا♥️💓 ؛Thank you💝
@ChadsPrep Жыл бұрын
You're welcome :)
@natebergfeld37002 жыл бұрын
Me saying "Schiff base" until I figured it out LOL
@ChadsPrep2 жыл бұрын
👍 👍 👍
@jaimeirigoyenlopez58845 ай бұрын
hahaha I still have not figured it out
@fernandasiordia7933 жыл бұрын
Thank u,!!!!! 👩🏫
@ChadsPrep3 жыл бұрын
You are welcome, Fernanda!
@nilsnickname44554 ай бұрын
Hello Chad, I have a question according to the acid catalyzed 6 step mechanism of the imine formation. Why does the proton transfer not happen intramolecular? Why won't the quartenary ammonium ion give a proton direct to the geminal alkoxyd anion? Isn't it much faster and therefore more probable when molecules don't have to "find" each other?
@cardiacmyxoma40733 жыл бұрын
Thank you so much!
@ChadsPrep3 жыл бұрын
You're welcome!
@laura5878 Жыл бұрын
What's your fav functional group?
@ريحانةريحانة-م3غ10 ай бұрын
Hi Dactor Why only primary amines can be formation the imines!
@michaelowogowog8518 Жыл бұрын
hahaha i don't know what happened in 21:51 but it was funny specially in 1.5 speed
@ChadsPrep Жыл бұрын
Normal or 1.5x - either way, a silly moment for all to enjoy!
@nilsnickname44554 ай бұрын
Hello Chad, I guess, that your reaction mechanism isn't completey valid. You can't attack with the N-nucleophile before having protonated the carbonyl-oxygen atom. If you do so, the microscopic reversibility wouldn't be maintained. When you set up the reaction for the back reaction, i.e. for the imine hydrolysis, you will see, that it isn't possible to get a molecule with a positive charge on the nitrogen atom and a negative charge on the oxygene atom at the same time!
@zainaba72472 ай бұрын
THATS A SCHIFF BASE
@weewaa5923 жыл бұрын
Wouldn't an intramolecular reaction between the -ve charged O be more efficient to get rid of the nitrogens +ve charge by reacting with an excess hydrogen? @ 6:30 on the video, thanks.
@peybak3 жыл бұрын
That's a good observation but that the oxygen is too close to Nitrogen do that. My guess is that it could happen if N and O were beta to each other, or even farther on the same molecule.
@weewaa5923 жыл бұрын
@@peybak Thank you for the insight, sorry for the long response