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Thank you very much for the compliment! 😀

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Sir please reply

Tum mass spectrometry, organic spectroscopy, and aromaticity ke playlist dekh lo. Inn topics se maximum questions puchte h. All videos are of 5-20 min duration, you can finish all three in 1-2 days. Rest you can also solve free mock test in IIT JAM chemistry playlist. Hope this helps! All the best for the exam 😀

@ thank you sir

Thank you 😊

You're welcome 😊

Yes, you are right. They have just focused on Re and Si face concept and accordingly the absolute configuration is incorrect. It should be S but absolute configuration is R. I might make another video on this topic for better clarification and understanding with some other examples!

Ok nice 🙂

Thank you 😊

Thank you very much 😊

No, hydrazine is NH2-NH2

It is a good question. Molecule 3 is also chiral although it does not have an actual chiral centre. The overall molecule is chiral, as carbon joining two rings is sp3 hybridzed. It falls in category of other chiral molecules (without chiral centres) like allenes, cummulene, biphenyl. This type of molecule like c is called spirane.

Yes, by mistake I have written 0.05 instead of 0.005. Calculation is correct, you can also try for yourself

Thank you

Thank you very much for the appreciation 😊... I hope for the same!

Yes it is antiperiplanar. You have to rotate in such a way that both H and Br are in same plane and at 180 degrees (anti) to each other. You get E-alkene as the product. You try yourself, if you don't get. Mail at chemazonchemistry@gmail.com for solution. I will send you.

Kyuki upload nahi kia h. Will upload soon

@Chemazon yes sir😊😁

Yes sure. I use XP pen tablet and microsoft powerpoint for making slides

@@Chemazon thankyou sir you are very kind...i wish for your channel to reach each and neddy students apart from that you have very good knowledge in organic, physical,inorganic. Your concepts are crystal clear. Thankyou sir.👏👏👏

@girishverma2113 Thank you very much for the kind words. Keep studying hard, be successful, and reach greatest heights! 😊

Thank you so much 😊

Very happy to know that... You can watch playlists as well based on particular chapter or topic

Thanks

Thank you 😊

Thank you 😊

Thank you so much for kind words and appreciation 😊 Means a lot

Thanks, happy to know that 😊

Ok sure... I will make video on this topic!

@@Chemazon thanks alot sir

Yes you are right! If u consider planar structure then ans is both K and L and only K if chair form is visualized.

Thanks for the appreciation, happy to know that 😊

Anti-aromatic hai kyuki vo huckel's rule follow nahi karta

@@Chemazon ok , bhaiya mera ak doubt or hai- fulvene non aromatic hota hai ki anti aromatic , or agr non aromatic hota hai to q?

@Sanatani585 It is non-aromatic based on experimental studies and negligible anti-aromatic character. You can read more in this page: chemistry.stackexchange.com/questions/82175/how-to-explain-non-anti-aromaticity-in-fulvene-with-the-help-of-resonance-st

Thank you so much for your kind words 😊

Thanks 😊

Thank you so much for kind words ☺️

Glad it was helpful! 😊

Thanks 🙂

Thank you very much for the appreciation 😊

Yes you are right, Xe can form maximum of 8 sigma bonds to form XeF8, which then react with F- to form XeF8- and not neutral XeF8.

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You're welcome 😊

Thanks 😊

Thank you so much for your appreciation 😊

Thanks 🙂

@Chemazon thank you so much dear Sir ji for your warm response

Thank you so much for your appreciation 😊

Welcome 🙂

Thanks 😊

Thanks a lot! Wish you all the best for your academic career 😊

Yes you are right, I wrote extra methyl by mistake. It should be only one methyl group attached to S. Thanks for pointing out!

I duly appreciate your work👍

Thank you so much 😊

Welcome 🙂

You're welcome 😊

Thanks 😊

Sure... Thank you so much for appreciation 😊

Thanks