Amine Synthesis Reactions
Vložit
- čas přidán 11. 05. 2018
- This organic chemistry video tutorial provides a basic introduction into synthesis reactions of amines.
Here is a list of topics:
1. Conversion of Alkyl Halides to Primary Amines Using Ammonia
2. Azide Synthesis of Primary Amines
3. Synthesis of Primary Amines Using Reduction of Nitriles By LiAlH4
4. Exhaustive Methylation
5. Gabriel Synthesis Reaction
6. Reduction of Nitro Groups to Primary Amines
7. Reductive Amination of Ketones & Aldehydes to Secondary Amines
8. Imine and Enamine Formation Reactions
9. Acylation Reduction to Form Tertiary Amines
10. Hoffman Rearrangement Reaction
11. Curtius Rearrangement Reaction
12. Hoffman Elimination Reaction Mechanism
13. Cope Elimination Reaction Mechanism
14. Conjugate Addition of NH3 to alpha beta unsaturated ketones
Subscribe:
/ @theorganicchemistrytutor
Access to Premium Videos:
/ mathsciencetutor
/ mathsciencetutoring
New Organic Chemistry Playlist
• Organic Chemistry - Ho...
Final Exams and Video Playlists: www.video-tutor.net/
Full-Length Math & Science Videos: www.patreon.com/mathsciencetutor/collections
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
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.
Been struggling with this until u came along. Thank you♥️
Perfect timing, just finished this chapter in class
ربنا يرزقه الاسلام والجنة يارب!
I THANK THIS TUTOR FOR THE BEST FREE COURSES ON CZcams
Thank you for using actual reagents in your examples for some reason no one else does that !!
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
Am from Kenya and your videos have really helped me alot🥳
I finished my quiz in 15 mins because of you! GOD SENT!
tq so much sir its quite helpfull
MAY GOD REWARD U
Thank you once again.
Thank you Tutor 😎🧪
Thank you and thank you
थैंक्यू सर 😊🙏
Great!
Saving lives since Chemistry 101- Organic Chemistry 407🎉😂❤
Why doesn't the N2H4 stay in a triple bond?
29:01 mechanism rx amine with hydrogen peroxide
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 ✌️
class is very nice sir thank you ,please little louder
if you and dave will open a school ill send everyone and their mother to study there.
Sir plz send a pdf file of all the rex if possible
or suggest any source
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
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
11:45 did you mean 2° Amine? ??
no it's primary cause the N makes a bond with 1 carbon
do I momresiz these ?
Yess!
Wow.
i like ketones
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
omg
1st comment like
3rd like
hehe 6th like
I don’t get it
First comment
First replay
no 2nd comment
00 l
Methamphetamine tutorial
If Ben Shapiro was a chemistry teacher