The longer I get into my all-nighter, the more Professor Dave could like... get it.

i love you professor dave

thank you so so much prof , you simplified organic chemistry for me

Maybe regiospecificity for the a potential halohydrin product should have been mentioned for the third reaction. For anyone who may be watching the video and wondering, it follows a Markovnikov situation where the OH group will attach to the more substituted Carbon.

Prof, before I turned to KZfaq channel learning organic chemistry chem was a hard nut to crack,but now, it's ' a walk in the pack' thanks😊

Hydrohalogenation? More like "Hey, these are great videos; go watch them!" Thanks again so much for making all of them.

I hate Organic Chem but I also love it because of how intricate it is. I mean heck if I watched this video 5 months ago it would seem like you’re speaking a foreign language😂. Great content though, I’m glad there are people like you out here man.

professor dave you the GOAT! Greatest of all time!

Thank you so much! your videos are greatly appreciated!

These videos are so helpful! Thank you Dave you rock

you're saving my life in OChem rn youre the best

Thank you!! I actually know what's going on now.

Wooow,, it's organic chemistry made simple, Am in light now no more darkness in organic chemistry

1 I personally think it would be better Professor Dave places more elucidation on the "halonium ions": how they take out a lone pair to form those C-X sigma bonds and then to form the three-membered ring. 2 I learnt that there is nonetheless regiochemistry involved, not because of the outcome of a dihalide. There is regiospecificity when the leftover bromide anion decides which "partial carbocation" in the ring to attack. The more substituted partial carbocation factually gonna get the bromine first. 3 I think it would be better if you display the anti relation of the bromines on a planar structure--with a cyclohexene--for visualization purposes. This way people better understand the stereochemistry. Last but not least, I have one question, why the bromines are in anti relation, why the other bromide(halide)has to break the ring from the opposite side of the bromonium(halonium) so it resembles Sn2, is it because only in this way can we have a anti relation of the bromines that offers the molecule least steric hindrance?

There was no intro?! Y?

6:06 Chapter on DIHALOGENATION ;)

u r superb!!!!thanks for the explanation sir ....

Good

Teacher please help me: when you have ethene and chlorine reacting occours and electrophilic addition. Why? Is there any video explanning this kind of reaction? I thought that would happen a homolytic addition, but no. Im from Brazil and in KZfaq I didnt find any video explanning this in my language so im trying to search in other languages. Could you help me please?

4:35 where did the H+ go after he took the electrons?

you are a star!

u can rotate one chiral centrum, then u ll get a meso configuration. with any trans alkene with symmetry substitutes u can ve a meso configuration, right?

sir can u make video on nucleophilic addition and substitution

Bro honestly you look like Jesus.... Come save me

What about Br2(aq)?? Where does the OH and Br go to?

thank u so much!!!

he is the second coming

I cannot thank you enough

plz show the carbon don't draw only bond

You're awesome

Do you teach outside the videos? where are you from? Lets toke one and talk chemistry man.

I'm more interested on what your forearm tattoo means....

thank you Jesus

G-d bless you Professor Dave!!

You Mr. , look like a hefty Joe Allen , although you are American . Anyways good videos , and nice explanation . Keep up the work 👌

OMG you r becoming bald😭😭😭😭!!r u losing hair sir😰😭😭😭😭😭😭😭😭

Is he jesus?

uhh..whuh..uhh