Видео

Thanks for helping us❤.

Really the best content on youtube for organic chemistry

Sir your way of teaching is excellent..❤ but you put videos in an irregular way.....no proper sequence followed....

What if its in the side this is the so important here

Watching this 11 years after but the stuff in it was super

Nice, thanks. But you did not change the position of Cl and methyl group when you flipped the compound.

this is literally the best fischer projection video i've watched and the ONLY one i've understood thank you so much.

thank you so so much for this . I can not thank you enough .you made this concept really really easy .

So so helpful and clear explanation, great video. Would the the conversion of OH to OTs be an SN2 mechanism then ?

It was helpful. Thank you, Sir.

This videos was very helpful. ❤

I found this video very helpful. ❤

It's very marvelous and interested

wouldn't cl and h be swapped to fulfill the r rotation on the fisher? if its drawn h-cl, doesn't it make the viral center have s rotation?

Really needed this today, thank you sir

THANK YOU THANK YOU THANK YOU ANDDDDD THANK YOU!!

Read your bible! (KJV, preferably) ♥‎‎ ‎

‌That was really great thanks a lot❤

thank you!!!

😊

thanks a lot for this amazing video also we learn this in high school in india haha

I searched a lot for this video and find it here. Thanks

Thanks, i really needed this video! I have sat in the auditorium listening to lectures, and spent a long time trying to figure this out. But in the end it took only ten minutes 😀 This is the way to teach things!

Omg most useful Ochem video I have so far seen :) great job, thank youuu

THANK YOU SO MUCH!! This makes sense!

great video

The wedge on the hydrogen is pointed the other way, does that make any difference or was it just drawn funny?

Only video that helped me tbh so much simpler than the other ways

sir please give me your whatsapp number because my organic chemistry is so poor so I can solve my query with your help🙏🏻.

I have got a paper tomorrow wish me luck 😅

Does Inorganic Chemistry also use Reagents as does Organic Chemistry?

Tysm ☺️

Really good job explaining it (even if that was 9yrs ago)! 👏 Explained it waaaaay better than my "Orgo I" professor!🧪👍 And one more thing, using cats explained the ideas in a crystal clear way. 👌

Wow this was very helpful, I now know how to assign s and r configuration 🙏

👏🏻

in the pka table water is shown as a poor leaving group, but right after it's shown as an example of a good leaving group (?) so which one is it then?

THANK YOU SO MUCH THIS HELPED ALOT!!😀

WHY ?C6H5OH DON'T REACT WITH SOCL2 ?

Turns out my toxic ex is a terrible leaving group... she never leaves me alone no matter how hard I try 🙄😂

Thank you so much

My teacher told that it is necessary to have heating condition for elimination reaction to take place otherwise reaction will proceed via SN2 mechanism could you clear my doubt please...

I LOVE YOUR WEBSITE, would be so lost without it omg.

THANK YOU 🙏🙏🙏

do you still do tutoring??? :) dying gr 11 chem student here

Why did I not just think of this?? Loll

This is so clear. Thank you

I could just imagine it in my head as a small CH3 group being able to fit beside the tertiary carbons, being small enough to fit like a puzzle piece; but TBuO being too big to fit between the 3* carbon and instead having to settle on the 1* carbon having nowhere else to go.

Many thanks!

God bless you, man. You saved me.

Thank you, thank you, thank you , thank you! You explained that better in ten minutes than my professor did in a whole lecture