If the world doesn't end, and youtube and the internet still exists in the future, then your videos will be helping people long after you're gone. You would've helped thousands, if not millions! You should be very proud of that! Thank you! P.S. Sup people from the future!
Thank you so much for your videos. I’ve just know you recently but really being addicted to all you said because they are perfectly capable to understand.
i loved this video :) this is the best video u ever puplished i mean to me this is what i m looking 4 i dont want mechanisms i want quick revisions where u summarize 10 reactions in 1 video cause in my college we are not asked for mechanisms only the end product or we have the products but we are asked for the reagents please we need more videos like this specially for furan and pyrrole and thiophene
QUESTION...........IF ANYONE knows the answer it is my HERO the organic chemistry teacher. Do you have a video on the mechanism of NH4Cl and formaldehyde?????????? How does the imine get reduced?????????????????????????????? If i protonate the imine to make an iminium ion then it is already positive........so how does the other hydrogen get on there. There are NO hydride anions in solution. I can not protonate twice...............ALSO GREAT VIDEO
Organic Chemistry - Video Lessons: www.video-tutor.net/organic-chemistry.html
If the world doesn't end, and youtube and the internet still exists in the future, then your videos will be helping people long after you're gone. You would've helped thousands, if not millions! You should be very proud of that! Thank you!
P.S.
Sup people from the future!
hi
Hai
What's up from me too,i'm prolly dead
"long after your gone" hahaha
FACTS.
Clear and simple summary that covered everything you need to know about Amines rxns at a college level. Thank you so much for your work. :)
I AM UR BIGGEST STUDENT FAN FROM PALESTINE
Hey. Hope you are okay
U ok?
Hope you're okay man. Free Palestine
Quit whining please..
Stop grabbing sympathy on an educational video
I wish you are ok.. pray for palestine
I THANK THIS TUTOR FOR THE BEST FREE COURSES ON RUclips
Perfect timing, just finished this chapter in class
Thank you for using actual reagents in your examples for some reason no one else does that !!
Am from Kenya and your videos have really helped me alot🥳
Thank you so much for your videos. I’ve just know you recently but really being addicted to all you said because they are perfectly capable to understand.
i have always loved your videos, you explain stuffs in an easy way you make things look easier than my lecturers . may God bless you.
ربنا يرزقه الاسلام والجنة يارب!
Been struggling with this until u came along. Thank you♥️
i loved this video :) this is the best video u ever puplished i mean to me this is what i m looking 4 i dont want mechanisms i want quick revisions where u summarize 10 reactions in 1 video cause in my college we are not asked for mechanisms only the end product or we have the products but we are asked for the reagents please we need more videos like this specially for furan and pyrrole and thiophene
I finished my quiz in 15 mins because of you! GOD SENT!
MAY GOD REWARD U
This is more entertaining than most movies hahaha
Saving lives since Chemistry 101- Organic Chemistry 407🎉😂❤
29:01 mechanism rx amine with hydrogen peroxide
Thank you Tutor 😎🧪
tq so much sir its quite helpfull
QUESTION...........IF ANYONE knows the answer it is my HERO the organic chemistry teacher. Do you have a video on the mechanism of NH4Cl and formaldehyde?????????? How does the imine get reduced?????????????????????????????? If i protonate the imine to make an iminium ion then it is already positive........so how does the other hydrogen get on there. There are NO hydride anions in solution. I can not protonate twice...............ALSO GREAT VIDEO
Thank you once again.
if you and dave will open a school ill send everyone and their mother to study there.
थैंक्यू सर 😊🙏
Thank you and thank you
class is very nice sir thank you ,please little louder
Great!
11:45 did you mean 2° Amine? ??
no it's primary cause the N makes a bond with 1 carbon
at 26:19 can you react the cyclohexylamine with 1. NaNO2,Hcl,0C 2. H3PO2, to get the cyclohexane?
Nope. Sandemeyer reaction is only limited to aromatic amine, and cyclohexylamine is not an an arylamine.
@@jonelpontica2628 Bro I graduated college years ago....
@@zaidsaud5563 haha
@@zaidsaud5563 and i am studying this in 12th grade
@@jonelpontica2628 ✌️
Wow.
Sir plz send a pdf file of all the rex if possible
or suggest any source
Why doesn't the N2H4 stay in a triple bond?
9:39 if you basically increase the ph of the sol. 😂
I had a chemistry joke I wanted to tell but it was too basic
@@ZackAG and i wanted to tell a sodium joke but Na
I am working on a reaction with TOFA and Different amines, every reaction turns to wax at room temperature, anyone have any suggestions?
C6h13n maybe?
EPO 593294A1
do I momresiz these ?
Yess!
i like ketones
Methamphetamine tutorial
I don’t get it
omg
3rd like
hehe 6th like
First comment
First replay
no 2nd comment
1st comment like
00 l
If Ben Shapiro was a chemistry teacher