Sir. I have one doubt at 10:43 minutes of this video? if the -ve charge formed near to the withdrawing group then the electron density of dienophile will diminish and if the +ve charge formed near to the electron donating group at diene will decrease the +ve charge density. So the ortho product formed first is not possible but meta product is feasible. if my perspective is not correct please correct me...
Dear Ganesh... thank you for watching many of my videos and deligently commenting on them. Regarding your query....first part of your assertion is correct. In fact that is what we want. Out of the two cycloadding partners, one should be electron rich and the other should be electron deficient to reduce the energy gap between HOMO and LUMO. That's the purpose of hooking up the electron pulling and pushing groups with the dienophile and the diene.
Sir, if any one watched ur video, really they get interest towards the subject. Such a wonderful teacher u r.
Thank you mam.
Thank you very much sir.
Great work
Give trb video sir.excellent teaching sir
Good teaching.. plz avoid back side noise
Excellence presentation skills Sir .......really a good mentor or teacher would reduced burden of students
Best video ever on pericyclic rxn👌👌👌
Thank you so much sir ... For ur clear explanation of this topic.... I was very confused with endo and exo... Now I some idea regarding this.....
Thanks sir unloading this please upload more question answer for iit jam 🙏
At mark 10:46, can you explain why negative charge to electron group and position charge to electron donating group? I thought the opposite is true?
Excellent sir
Thank you sir.
Can you explain the stereo chemistry of Cycloaddition reaction
Suprb sir.. Very useful..
Great explaination sirji...🌹
Thank you
Sir. I have one doubt at 10:43 minutes of this video? if the -ve charge formed near to the withdrawing group then the electron density of dienophile will diminish and if the +ve charge formed near to the electron donating group at diene will decrease the +ve charge density. So the ortho product formed first is not possible but meta product is feasible. if my perspective is not correct please correct me...
Dear Ganesh... thank you for watching many of my videos and deligently commenting on them. Regarding your query....first part of your assertion is correct. In fact that is what we want. Out of the two cycloadding partners, one should be electron rich and the other should be electron deficient to reduce the energy gap between HOMO and LUMO. That's the purpose of hooking up the electron pulling and pushing groups with the dienophile and the diene.
Sir stereochemistry .. thank you
2+2 addition is also diels alder reaction or not? Pls explain this doubt
No friend. It's not field alder
QUESTION R HARD... ...sir pls upload one separete video fr diels alder rxn
For JAM or CSIR or TRB?
@@chemistryvoice981 trb sir
Ok mam..sure
Why can’t the diene should be LuMo ?
Questions are hard sir, pl upload trb oriented rxns sir
Actually this video I uploaded for IITJAM. ....ok I'll make separate one for TRB. Thank you
@@chemistryvoice981 thank you sir