It is cool you give us also the MECHANISM of a anorganic redox reaction, it's not usualy seen, I actualy failed an internship for beeing unable to find JUST one Websource saying me how the mechanism for a certain redox react was. But alas, it was not the one shown in this video (I had to search the oxidation of Toluene to benzylic acid by KMnO4) but thank you anyways, for the ones needing this metal mechanism your video is suposedly their ONLY chance.
my professor loves making us learn upwards of 10 mechanisms for any given exam so he can ask a multiple choice question that presents four different scenarios which are PART of any of those mechanisms. We are supposed to pick the two incorrect ones lol. I had to learn mechanism patterns so fast
whats the advantage of the radical mechanism of the sandmeyer reaction in comparison to the cation-intermediate? sure, it would not explain the usage of copper. but is the radical intermediate maybe more stable than the cation-intermediate?
I think its because if the O minus took the H we get OH which is a terrible leaving group where as water is a very good leaving group. In order for the OH to be gone we are gonna need to convert it into something that is a very good leaving group or it wont work.
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keep up the good work proff, this is THE best chem channel I have ever visited. love from India
This Channel needs million views and millions subscribers for his hard work !!!!
Your Understanding of Chemistry is on a whole other level... Damn!!!😂🙇🏽♂
It is cool you give us also the MECHANISM of a anorganic redox reaction, it's not usualy seen, I actualy failed an internship for beeing unable to find JUST one Websource saying me how the mechanism for a certain redox react was. But alas, it was not the one shown in this video (I had to search the oxidation of Toluene to benzylic acid by KMnO4) but thank you anyways, for the ones needing this metal mechanism your video is suposedly their ONLY chance.
Phenomenal. Great research on this vid, and it’s a shame mechanisms are not taught in as much detail at most, if not all, educational institutions.
my professor loves making us learn upwards of 10 mechanisms for any given exam so he can ask a multiple choice question that presents four different scenarios which are PART of any of those mechanisms. We are supposed to pick the two incorrect ones lol. I had to learn mechanism patterns so fast
Thanks sir u r awesome...love uh...idont watch any one othrrs vedios.... live long sir..
Thank u bro !!!!!!!!!!!! U saved me(literally).
It's so perfectly congratulations Sir
thank you every much
Important question: Where is the OH- that we are supposed to add in the reduction of nitrobenzene to phenylamine
Wonderful lessons very elaborate
Can you perform this reaction if the molecule has an Ester?
Amazing!
Why does HCl not behave as a radical with the radical nitrogen?
great thank you a lot
Many thanks sir..so clear n brief...very good exp.
In n=o why does o positive doesnt attract nh2
Kindly learn to make the proper shape of benzene ring. Btw Nice explanation!
So how was your JEE?
whats the advantage of the radical mechanism of the sandmeyer reaction in comparison to the cation-intermediate? sure, it would not explain the usage of copper. but is the radical intermediate maybe more stable than the cation-intermediate?
Sandmeyer Reaction 22:56
in first step of mechanism ,why oxygen with negative charge does not abstracts h+??while reacting with nitric acid and sulphuric acid
I think its because if the O minus took the H we get OH which is a terrible leaving group where as water is a very good leaving group. In order for the OH to be gone we are gonna need to convert it into something that is a very good leaving group or it wont work.
Beacause O- is in resonance therefore it stable so the other oxygen bonded to h and n abstracts the H atom from HCl
Well sandmayer became samurai