Thank you so much sir.... I was really worried about this whole concept but you explained it thoroughly in such a easy way.... Forever grateful to you🙏
Meso tartaric acid is optically inactive. So can we say that the C2 and C3 of this molecule are both chirotopic and stereogenic because there exist a local chiral environment for both of the carbon atoms?
Sir how it is passible that in a chiral molecule every substituent is chiral because in case of Allen's not every point is chiral due to two changes group
Chirality is the property of a molecule as a whole..so every point/atom/substituent resides in a chiral environment in a chiral molecule and is called chirotopic.
I couldn't understand the concept of stereogenic centres but after watching this video I got it easily.....Thank you Sir
Thank you so much sir for explaining this topic so beautifully and in an easy manner..Forever grateful to you🙏
Thank you so much sir.... I was really worried about this whole concept but you explained it thoroughly in such a easy way.... Forever grateful to you🙏
4:56 inversion centre present so not optical active it's optical inactive because centre of symmetry are present
Thank you sir.
Meso tartaric acid is optically inactive. So can we say that the C2 and C3 of this molecule are both chirotopic and stereogenic because there exist a local chiral environment for both of the carbon atoms?
Thank you sir for this helpful discussion on chirotopicity and stereogenesity . It helps me very much
Really helpful for me.
Why have u done 180 rotation for finding stereogenic centre in fischer
because they may have homomeric relationship .... so we must check whether it is returning to the same molecule or not
Can u further explain about chirotopicity
Sir there is apossibility ,achirotopic /nonstereogenic
thankyou
Sir how it is passible that in a chiral molecule every substituent is chiral because in case of Allen's not every point is chiral due to two changes group
Chirality is the property of a molecule as a whole..so every point/atom/substituent resides in a chiral environment in a chiral molecule and is called chirotopic.
Thanks for making the life easy
Thank you sir ❤️🙏🏼
Thank you so much sir
Achorotopic/non stereogenic center is possible?
Yes it is possible...there are many examples...one example is propan-2-ol, where the C2 is achirotopic and also non-stereogenic
Iit teacher 💥💥
Thank u sir
Lec 6
chirotopic
copied from nptel