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thank you boss

CLODUDY BFDI

this was exactly what I was looking for! Thanks a lot.

The esercises were good for revision/study, explanation fast and clear. Well done!

I’m a bit confused on why the configuration went from trans to cis at 8:38 ?

Taught it to me when my professor didn't have time to. Thank you so much!

Nice explanation. All understood. Thank you.

Thank u so much man you are the best and a great teacher

It’s a good piece of explanation. Thanks a lot.

Thanks for video. In my opinion you missed one important thing, syn-addition/elimination

9:44 i got really confused in this part, you wrote that experimentally : primary = 64% and tertiary = 36% , after that you said that tertiary is 5x more likely to form during chlorination, how is that possible if the percentage of tertiary experimentally is less than the percentage of primary?

i know u stopped uploading but i gotta thank u for this my exam is next week and ur vids are really helping

what is the effect of -SH (Benzenethiol) on EAS?

Underrated

@4:15 isn't the Br at the para not the meta?

This is so well-organized it is very helpful to understand my orgo synthesis class Thank you sm!!!!!!

Sir but how does molecular orbital theory ignores resonance hybrid structures??

High quality organic chemistry videos

Loved it!

Hello! Can you explain about Oxidation of isopropyl alcohol to acetone (Nh4Cr2O7 Thank you!

Why does the arrow-pushing notation for electrons fall apart when dealing with transition metals?

Not bad, could have been a little more in depth with the mechanism but still great. Thanks

Can you give me some more natural cycloalkanes with its therapeutic uses

Thank you so much, I was so lost in lecture

Is this because you consider the HOMO of butadiene?

thank you

in kanjuruan stadium riot accident, 129 people killed because police shot tear gases near supporter tribune

Great Explanation. Thanks, Sir.

this is really helpful! thanks for the video

How to choose? More like “With this content, you can’t lose!”

Seems like it takes an enantiomer to get an enantiomer…

Diastereomers? More like “Definitely great knowledge for sure!”

I really didn’t expect to see this kind of story in an ochem video, but I’m so glad I ran across it!

Reactions of epoxides? More like “Really great information inside!” I’m very glad I found your videos; they’re great to use to review ochem.

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Plzz bring advance optical isomerism

Tear ⛽

Amazing!! Thanks 😊

such a great video!!

Second

first

This is so cool!! Thank you so MUCH!!!

im sad to see u dont have a lot of subscribes, ur videos are very helpful! good luck growing ur channel :)

Nicely done. Some of your videos are clearer and easier to understand than khan academy and crash course.

some love for the man who helped me reach my deadline <3

I believe there's a mistake towards that step that turns the diol into a carboxylic acid. We are using H2CrO4, yet you drew HCrO3. They accomplish the same thing here, mechanistically, I would assume, but this is a discrepancy.

good job

Nice video, I would like to ask, why does alkene always need a electron withdrawing group come along with to activate this reaction?

Nice explanation. Keep it up

Thank you!