I appreciate the work you put into these videos, unfortunately i still suck at organic lol.

Hey Professor Dave! Thanks so much for all your help with Orgo 1 and 2 this year! Your concept videos were awesome. Wouldn't have been able to get though it successfully without your help!

Only part of organic chemistry that dare I call, “fun”

This is like a top down approach, you start from the finished product, and derive its components.

Professor Dave finds lots of " medicinal" compounds in nature.

Whenever I need a little brush up of any concept ,your videos help me out Good job pro

thank u sir...really appreciated ur vid....its goin to help me in my xms...

Have you ever considered doing meet and greets in CA professor Dave? Love your videos!!

love it so much, so helpfull thank you from Indonesia

this is really helpful,thanks as I did not understand this in wikipedia and quora thanks!!😁😁👍👍

You're the best...understood

Your videos help a lot..Thank you so much.

very beautiful….. do you have other videos like this? With much more complex molecules?

Can you do an excercise to obtain a heterocycle compound? Thanks for your content

And also, why do we need to use PCC if the grignard reagent already kicks out the double bond with the O--thus making it OH??

Hi there genius! Please help me solve a query in organic chemistry.... Please... "RUTIN" or "Rutoside" is a bioflavonoid with the formula C27-H30-O16, it is found in plants like Buckwheat and eucalyptus.. My question is.. " Is it possible to manufacture "RUTIN" synthetically in a lab? without actually using the plant extracts.

For the first reaction, should we use MgCl? When you radically halogenate the propyl group with Br, it is more selective for the secondary carbon and that would yield a different product. We should use Cl because there is only a negligible difference between the selection of a primary vs secondary carbon??

thank you so much

Thank you sir ...for helping me out

thanks

Thanks!

Thank you!

Thank you Sir for this information

could we just react the DB at 6:30 ish with 2 equivalents of O3 to create two ketone groups and turn those into alcohols with NaBH4 to create our alcohols?

Can you do retrosynthesis for aldol condensation reactions?

how do i know which reaction to apply when doing organic conversions ?

Why couldn't just start the first one as 1-pentene and reacted that with H20 and H2SO4?

Thank you very much!

You are a super hero!!!

Which book is best for retro synthesis please advise sir

Thank you so much sr♥️♥️♥️

If I had looked at this earlier I would have done Honours by now.

Its really helpful......

I have a restrosynthetic synthesis exam can you help me with some links that could guide me please

Pls give me the name of refrance book for parcticing retrosynthetic analysis........

Is there a good place to drill these practice problems? I've taken a look at your practice problem videos. I've also searched and found some practice sheets, but they aren't really enough for me. Is there a site or app that would give me problem after problem for me to practice?

Sir what is the synthetic equivalent of co groups tell me

sir ,could you please post a video on synthesis of peptides by sheehan's method

bro is Noah Kahn if he was a chem god

What about use of retrosyntesis method to make cyclic compunds?

slaam sir

Best

👍❤