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Organopalladium Chemistry (Suzuki Reaction) 

Mandeep Singh (ChemoSpecific)
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23 сен 2024

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Комментарии : 26   
@abhinavprasad4093
@abhinavprasad4093 3 года назад
Best video I found on RU-vid. Thanks sir 🙏🙏🙏
@ChemoSpecific
@ChemoSpecific 3 года назад
Glad you liked it
@dattatraykhamgal6695
@dattatraykhamgal6695 3 года назад
This is the best Video on Suzuki coupling reaction👌👌👌
@ChemoSpecific
@ChemoSpecific 3 года назад
Thank you so much 😄
@allforminside7359
@allforminside7359 3 года назад
Best vedio .. highly content full and pricesly explained..pls make some more vedio on cladyen book ..
@sejalmahajan3630
@sejalmahajan3630 2 года назад
Very well executed 👍👍
@ChemoSpecific
@ChemoSpecific 2 года назад
Shukriya
@dattatraykhamgal6695
@dattatraykhamgal6695 3 года назад
Very well explained 👌👌👌 Really like the sentence Most widely used in Industry over other pd reaction.Yeah That's true👌👌👌
@ChemoSpecific
@ChemoSpecific 3 года назад
Exactly
@sujaltripathi3830
@sujaltripathi3830 2 года назад
U r grt ❤️
@R_SINGH_BISHT.
@R_SINGH_BISHT. 4 года назад
Thanku veer ji ...saare examples ache se clear krne kr diye with other useful explanation... please uplod more question net and gate
@samirmo7494
@samirmo7494 5 лет назад
Awesome video sir
@Tnpscremembertricks
@Tnpscremembertricks 2 года назад
Good morning.. Sir... Nice explanation what is the reference books for this topic please tell me sir...🙏🙏🙏
@ChemoSpecific
@ChemoSpecific 2 года назад
I think it's from Nantz and Zweifel book if I am not wrong
@HarshPatel-xn6du
@HarshPatel-xn6du 3 года назад
Sir ek hi doubt hai...pure mechanism me pd L2 ke sath me dono Ligand cis kab rahenge aur trans kab rahenge. Aur reductive elimination ke liye cis hona jaruri hai??
@ChemoSpecific
@ChemoSpecific 3 года назад
I will say let's not get into the isomerization part (experiments has shown trans to cis mechanism happens especially on sonoghashira coupling). Because at times, there may or may not be depending on the reaction. Just remember the general mechanism or shall I say Remember this (1) oxidative addition (for which Pd has to be in 0 oxidation state) (2) transmetallation (3) reductive elimination
@souviksarkar1784
@souviksarkar1784 5 лет назад
Why Pd is widely used in organometallic reaction??
@ChemoSpecific
@ChemoSpecific 5 лет назад
Palladium also has a relatively low activation barrier between the oxidation states of 0 and +2 corresponding to the stable d10 and d8 configurations. These oxidation states are important for oxidative insertion and reductive elimination. The lower the activation barrier of the transition from 0 to 2+ and back again, the more rapidly these reactions can take place. The faster and more favorable these reactions are the higher the turnover rate for the catalyst. That apart, There are a lot of other metals that can do much of what Pd does, but cost a lot more- Ir and Pt come to mind. In recent times there has been a push to use first row transition metals (especially nickel, since it's in the same family as Pd) for similar reactions, with some success.
@souviksarkar1784
@souviksarkar1784 5 лет назад
@@ChemoSpecific Thank you sir. Very nice explanation.
@MOHIT-vr3zn
@MOHIT-vr3zn 4 года назад
@@ChemoSpecific great sir
@MOHIT-vr3zn
@MOHIT-vr3zn 4 года назад
@@ChemoSpecific great sir
@spchge
@spchge 3 года назад
Is it possible that he switches from english to indian?
@jaggu3149
@jaggu3149 5 лет назад
Thank you
@p.pchemistrybyprofessorpra9482
Thanks sir
@PRIYASINGH-wu4ur
@PRIYASINGH-wu4ur 4 года назад
👍
@Chem_hub.official
@Chem_hub.official 4 года назад
Must watch suzuki coupling #Like#share#Subscribe ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-Sp2Taghp9yA.html
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