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@alarcon9793
7 жыл бұрын
so difficult to find a good explanation for the hoffman rearrangement, thank you so much!
@salvadeng
2 жыл бұрын
This man knows how to make things understandable. May God bless you!
@ernestcheng1399
5 жыл бұрын
You know these videos are great when you dont have sound and you still understand what is going on.
@vnm5740
5 жыл бұрын
26 minutes-totally worth it.tnx man.
@amitdeshmukh1113
3 жыл бұрын
26min 27 sec and a few Milli second which U tube doesn't cares about.
@NikitkaDreamer
2 жыл бұрын
i wanna cry all this time i ignored Hoffman degradation and only thought about other ways to create primary amines, because of bromine but if chlorine works too... damn
@LordBrainz
5 ай бұрын
Actually, hypochlorite works as well
@michaelmiller8051
Жыл бұрын
I would really loved this more if it were in a playlist with all the other reactions
@frodouardnambajimana4002
3 жыл бұрын
That's extremely fascinating
@prof.husseinalhendawi6151
5 жыл бұрын
It is really awesome. Thank you very much.
@philipsoglo4143
6 жыл бұрын
Great tutorial was really helpful thanks...
@efsunefsane1301
4 жыл бұрын
Can you make a video about beckmann rearrangement to generate an epsilon-Caprolactam ? I wish you can read this message. 😊
@andreaxshadow4911
4 жыл бұрын
Can NaOH give an hydrolysis resation with the amide, attacking the carbonyl group?
@neechan8348
5 жыл бұрын
your lecture is very helpful for me ,thanks, sir
@ayushanand5221
4 жыл бұрын
Simp
@羅孟軒
Жыл бұрын
so tricky! but you still nailed it!
@محمدالحربي-ي4ص3ح
5 жыл бұрын
thanks very much you are the best bro
@potumnn
3 жыл бұрын
could hofmann rearrangement work also with secondary amines? to give us R-NH-R' ??
@Yannickwhething
3 жыл бұрын
No, it`s not simply not possible. Try the mechanism with a secondary amid, you should fail at the abstraction of the "second H-atom"/ the formation of the isocyante
@ChemoSpecific
4 жыл бұрын
If we treat N-methyl acetamide with Br2/NaOH, will we get N-Methyl methylamine
@ChemoSpecific
4 жыл бұрын
@Raj Kumar Answer is No
@potumnn
3 жыл бұрын
@@ChemoSpecific should we obtain dimethylamide?
@ilimselyardm9698
3 жыл бұрын
At the 21:53 why do we giving the partial positive oxygens hydrogen to another water molecule instead of partial negative oxygen (above the carbon) btw thank you sir for this good explanation Allah may bless you
@iconicguy5717
2 жыл бұрын
H2O generally attaches H to form H3O+ rather than attacking the partially negative oxygen to form the unstable products. Also, there will be repulsion between the oxygen of intermediate and oxygen's (of water) lone pairs.
@sandy69402
10 ай бұрын
lmao u can't just randomly send a hydrogen atom through space like that except in cases like tautomerism or formation of zwitter ion
@ilimselyardm9698
10 ай бұрын
@@sandy69402 Thank you
@ilimselyardm9698
10 ай бұрын
@@iconicguy5717 Thank you
@monalisaarshnirvi2953
6 жыл бұрын
Thank you sir. Your video was of great help to me.(:
@ajithajith2314
6 жыл бұрын
Brother one doubt, please explain me difference between molecules and compounds.
@saniyamulani3206
4 жыл бұрын
When same atoms combined together it form molecules and when diff molecules comes together it form Compound
@saniyamulani3206
4 жыл бұрын
Same moles of atoms forms molecule
@saniyamulani3206
4 жыл бұрын
Diff molecule forms compound
@shaikrafiq9498
4 жыл бұрын
@@saniyamulani3206 yes
@leen-7777
5 жыл бұрын
And thank you so much but i deviced you to make it easier
@ajithajith2314
6 жыл бұрын
Very thanks bro.
@Arjun-yz4sx
7 жыл бұрын
why does alkyl rearrangement happens?
@miroslavkaspar2246
5 жыл бұрын
Its driven forward by CO2 formation, the CO2 leaves the reaction as a gas, thus forcing the reaction to competition.
@neechan8348
5 жыл бұрын
thanks .
@Rudra-mm1qf
5 жыл бұрын
thank you.
@garrydhesi906
6 жыл бұрын
Awesome
@praharshinisai4944
4 жыл бұрын
Thank u!!
@hrishikeshdeore5340
6 жыл бұрын
book name ?
@lebogangmakhosi7637
11 ай бұрын
wow
@ugh-ye3yc
10 ай бұрын
14:53
@ajithajith2314
6 жыл бұрын
Please reply me
@leen-7777
5 жыл бұрын
But your videos are toooooooo long please make them shorter
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