its really simple..if u have to flip it to get the mnemonic form...then perform the addition of OH and the final product also must be flipped in such a way u did before doing the rxn, in order to get the correct spatial arrangement. If u flip it 2 times before the rxn to get the mnemonic form , then to arrive at the product with apt stereochemistry ,u have to flip the dihydroxylated product same two times . I think its as simple as that. U explained very well. Good going Thank u.
Very very well explained sir.especially the reason fr why 2 OH groups of similar stereochemistry cannot be written on same side was a good one.small things also matters alot,as a student we should know each and every reason,and we r lucky enough to learn it from you.thanku you sir
Exactly when we have to rotate or when we have to flip the molecule or it will depend on only conditions we provide or to get trans Rl or Rm acc.to that we have to manage
great sir ,very nice explanation ,you solve my tension ,thank you.sir plese teach us that part of perturbation theory of quantum because now time is very less.
hello sir here in this pending example large group is topp right side, so whether we have to it twice to make it correct form. can you please tell me stereochemistry of the final pdt if we are using DHQ2
sir what about asymmetric amino hydroxylation reaction ? The stereochemistry is same like assymetric dihydroxylation but still how do we know which one is major and minor product on which side amino group going to be attack ?
Gate chemistry I understand you are going through a hectic schedule......but the thing is your videos are really helpful for the aspirants like us....... that's why you get so much requests sir.... anyway hope you will cover the topic soon....🙂
its really simple..if u have to flip it to get the mnemonic form...then perform the addition of OH and the final product also must be flipped in such a way u did before doing the rxn, in order to get the correct spatial arrangement. If u flip it 2 times before the rxn to get the mnemonic form , then to arrive at the product with apt stereochemistry ,u have to flip the dihydroxylated product same two times . I think its as simple as that. U explained very well.
Good going
Thank u.
Sir u are just awesome ...Sir mujhe to bahut ache se smjh m aa gai thanku so much sir jiii🙂☺️
Very very well explained sir.especially the reason fr why 2 OH groups of similar stereochemistry cannot be written on same side was a good one.small things also matters alot,as a student we should know each and every reason,and we r lucky enough to learn it from you.thanku you sir
Explained really well, that concept regarding R & S Notatm of the 2 -OH group was really helpful as it was a hidden one, tq :-)
Exactly when we have to rotate or when we have to flip the molecule or it will depend on only conditions we provide or to get trans Rl or Rm acc.to that we have to manage
superb explanation sir.sir plzz make video on asymetric aldol reactn and tanabe sugano diagram
Nice sir and old do a video on new synthetic reactions remaining sir if u have time
great sir ,very nice explanation ,you solve my tension ,thank you.sir plese teach us that part of perturbation theory of quantum because now time is very less.
How do you get anti addition in one step? Doesn't the alkene need to be cis in that case?
superb sir...thanx
Thanks bro its truly required
Which book is good for Sharpless reactions
Thanku sir for such a wonderful explanation,sir by the way where ate study PhD,how many marks you got in msc, if you tell me I am thankful to you.
zimmerman traxler any video?
hello sir here in this pending example large group is topp right side, so whether we have to it twice to make it correct form. can you please tell me stereochemistry of the final pdt if we are using DHQ2
OK thank you sir..
Sir is it a name reaction??
In which playlist you have added this reactions???
Sir which book should be refer for net Jrf chemistry...
Sirji it is not mention in Question is alpha-AD mix or Beta-AD mix ? then how we predict reagent in exam
pls help on that.....it is imp
Nice topic
Sir , my organic chemistry base is weak..but you can make understood so easyly..So Thank u very much..
sir what about asymmetric amino hydroxylation reaction ? The stereochemistry is same like assymetric dihydroxylation but still how do we know which one is major and minor product on which side amino group going to be attack ?
wow that's great ..Thank you sir
chiral reagent and chiral auxiliaries are the most difficult topic in this
Good explanation sir..
Wel come
Sir plz suggest me basic books for inorganic chemistry
Thank you
Thanks sir u are awesome
Thank u sir suggest ne how I crack csir
sir plz do videos on pericyclic chemistry.....
Gate chemistry I understand you are going through a hectic schedule......but the thing is your videos are really helpful for the aspirants like us....... that's why you get so much requests sir.... anyway hope you will cover the topic soon....🙂