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why do we take the base as methyl acetate only?

hi

i read this mechanism in 2 books, read this mechanism on a site for 2 hours before getting frustrated and crying, now i have tears because i watched this video twice and wrote the reaction in my words and I UNDERSTOOD!!! KEEP UP THE EXCELLENT WORK!!!!!!!!!!!!!!!!!!!!!!!!

Kindly use 🎤 voice is very slow

Are you alive.....if then pin me

thank you for this sir!! best for jee advanced!!

Thank you. You made reductive amination look very easy... I searched for the mechanism for so long. Have a nice day sir.

Great explanation sir!

Just amazinn!

Super

Thank you very much sir for the best video of explanation more than atp star😂😂

Thank you sir

almost no one makes mechanism explanations on youtube as detailed as this, thank you very much sir :)

Good lecture explanation. Thank you

What of the first example?

sir what is the full form of IPSO

Well explained. ❤

Thank u sir ❤

Thankyou!

Thankyou sir 👍

Thanks🎉

Thank you very much sir it helped a lot for iitjee

How oxygen form triple bond

Water is not mentioned so why you have taken H2o as nucleophile

Thanks a lot sir. Genuinely the explanation is soo simple and subtle...loved it

Excellent

Well done....all the points well explained...jazak Allah

won't that leaving BF3O- grabs the remaining proton on the other end of the dithiol to give a S- species? Because I think BF3O- is more basic than RS-?

Nicely explained!

Thank you so much... was searching for these conversions!!!🙏

please start posting again, this is probably the best advanced chemistry channel on youtube

Great sir.. 👌👌👍

thank you sm ❤️

Excellent content Sir

Thank You Sir 😊

This simple concept of 'Mg','Zn' no one covered in the vedio about this topic. Thank you sir to discuss about this topic.

This is wrong more substituted enolate (Thermodynamic enolate) is stable than less substituted enolate (kinetic enolate). Less substituted enolate will form only when bulky bases like LDA or LHMDS in THF at -78°c. Unless this condition always Thermodynamic enolate i.e more substituted enolate always form. For more details please go through Clayden Book page no 601

Excellent explanation Sir🙏

Thanks

Very nice explaining 👍

Sir kindly tell us about nucleophile effect means either it should be strong or weak in SNi

Why ester reduced to alcohol instead of aldehyde at -78 ?

Thanks Sir. But Fischer are wrongly shown. Please check

The best Thanks a lot.

Great explanation

شكرا كان شرحاً مفيداً بالنسبة لي😍

Make a video on how to calculate the double bond equivalent of 2-methylbut-1,3-diene and cyclo-1,3-diene

Why this channel is so underrated 🥺

thank u so much ......i just read clayden and cofused in chapter number 23 ....(chemoselectivity)but now it is just crystal clear.....thanks a lot sir

Nice explaination