Your Sharpless Epoxidation method was absolutely awesome and I used it to get the same answers as my professor, who does the left habded rule! Thank you thank you thank you
Sir, in ur last video on Sharpless epoxidation d mnemonics you given was completely opposite than u discussed here ...priority of groups, observed carbon were also different...this seems to be easy to grasp
Please make a vdo on thermogavimetric analysis portion of analytical part .....please ....i want to get a complete idea to clear all the problem on csir net
The carbon to which u gave priority no. 2 is attached by a double bond. So it should be assumed that our central carbon is attached to 2 carbons. So i think it should be given priority no. 1
Sir, explanation is very good but this video is contrary to your previous video on Sharpless epoxidation.so I bocome confused which is right.plz tell which we should follow.
Sir, there's one more separate video of yours on sharpless epoxidation. And I guess, it was different what u taught there in that and in this video. Please correct if I'm wrong.
@@gatechemistry yes..just saw. You're literally doing a priceless job sir. Thank you so much. Sir, I'm scoring like 70-80 marks in mock tests. If at all I fail this time. Should I look to join some coaching institute or do more practice??
In case if OH is on upper side, then also we have to consider the face as it is or we have to arrange the molecule in such way that the OH COMES down and then assign the faces?
Sir u had told that(+)DET is Si face on a video which u had posted a while ago on asymmetric epoxidation. But is it Si face or Ri face sir? Here on this u have told as Ri face
Sir plz make video for organo lithiums.. chiral auxiliary and retro synthesis and analytical chemistry they all are scoring as you tell us in organic strategy video
But sir in ur earlier video of sharpless epoxidation, u told that +DET attacks from si face and - DET from Re face.... And also there u have given preference to double bonded carbon and not to alcoholic carbon.... Plz tell which one is correct
In shi epoxidation the stereochemistry is always R,R means above the plane or below the plane
Your Sharpless Epoxidation method was absolutely awesome and I used it to get the same answers as my professor, who does the left habded rule! Thank you thank you thank you
sir plz explain streochemistry of epoxide
Sir, in ur last video on Sharpless epoxidation d mnemonics you given was completely opposite than u discussed here ...priority of groups, observed carbon were also different...this seems to be easy to grasp
What will be the stereochemisty of trans alkene with jacobsen? Will it react?
Thank u so much sir❤️🙏
Please make a vdo on thermogavimetric analysis portion of analytical part .....please ....i want to get a complete idea to clear all the problem on csir net
stereochemistry of epoxides...
Sir please explain stereochemistry of epoxide .
YES SIR THANK YOU
The carbon to which u gave priority no. 2 is attached by a double bond. So it should be assumed that our central carbon is attached to 2 carbons. So i think it should be given priority no. 1
If alkyl group is present in place of hydrogen then to which carbon we give first priority
Is there any reference to this + DET attacks from Re face and - DET attacks from Si face....pleased
Sir, explanation is very good but this video is contrary to your previous video on Sharpless epoxidation.so I bocome confused which is right.plz tell which we should follow.
Sir please discuss question no. 100 of June 2015(set-A)
Unusual Sharpless reaction
Yes that seems some difference..
Sir, there's one more separate video of yours on sharpless epoxidation. And I guess, it was different what u taught there in that and in this video. Please correct if I'm wrong.
@@gatechemistry yes..just saw.
You're literally doing a priceless job sir. Thank you so much.
Sir, I'm scoring like 70-80 marks in mock tests. If at all I fail this time. Should I look to join some coaching institute or do more practice??
Make a short video on stereochemistry
Please upload video for nomenclature epoxides
in previous video you gave priority to double bonded C and here priority to C attached to O....?
sir plz make a video on sigmatropic rearrangement
Thank you sir.... God bless you....
And also on statistical thermodynamics crash course
In case if OH is on upper side, then also we have to consider the face as it is or we have to arrange the molecule in such way that the OH COMES down and then assign the faces?
Yes I want about r/s of epoxide
Sir u had told that(+)DET is Si face on a video which u had posted a while ago on asymmetric epoxidation. But is it Si face or Ri face sir? Here on this u have told as Ri face
Sir plz make video for organo lithiums.. chiral auxiliary and retro synthesis and analytical chemistry they all are scoring as you tell us in organic strategy video
It's visible to me.... thank u sir
After Epoxidation of allylic alcohol the epoxide ring is opened by hydroxy group or not
Sir plz explain stereochemistry of epoxide and also explain shi epoxidation with some examples
Sir explain the sterio chemistry of epoxides
make a vdo on quantum mechanics previous yr qs solution....pls
Sanchari Pramanik its on unacedemy
Stereochemistry of epoxide. Pls explain....
But sir in ur earlier video of sharpless epoxidation, u told that +DET attacks from si face and - DET from Re face.... And also there u have given preference to double bonded carbon and not to alcoholic carbon.... Plz tell which one is correct
Gate chemistry yes sir.... Got it... Thnx a lot for replying
Sir plz discuss stereochemistry of epoxide
Very nice explanation
thanku sir for awsome explanation
Sir but in earlier vdo which was already done on epxidation u said that +for Si face and - for Re face.pls check that sir..I am in little confusion
i think jacobsen me large or small group se mistake kr diya .....
Sir u say that + sing attack Re-face in this video but another video u say that - sign aatack Si- face why??
nice thank u....
nice thanks sir
Sir not visiable