Why? Why bro why? Why not exercise, go outside, read?! Like, unless this is what you are passionate about, or you just like learning new things, why 🥲.
this is due to the fact that the HCl bond is too strong to be broken to produce free radicals ( bond energy is 430.5 KJ/mol) while the bond energy of the HBr bond is 363.7 KJ/mol. In case of HI, although the H-I bond is broken pretty easily via homolysis, the iodine atoms so produced immediately react to form iodine molecules instead of attacking the double bond of the carbon atoms in alkene.
Markovnikov and anti-Markovnikov rules and yes, the more substituted / less hydrogenated carbon gets the Halogen in Markovnikov fashion ( not in presence of peroxide’s ROOR )
Because we want Br• radical for our next step, where it attacks the alkene. Some of the R-O• and some of the Br• do combine to form R-O-Br, but that is not required for us at the moment for the reaction. Hope it helped
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Are we gonna ever know who the legend behind these videos is?
It will be one of the mysteries of the Universe that will remain unsolved. 😢
Finished taking Organic Chem but still really enjoy watching these videos. Such a good teacher
dude seek professional help
Why? Why bro why? Why not exercise, go outside, read?! Like, unless this is what you are passionate about, or you just like learning new things, why 🥲.
once i get my PHD and pay off my school debts i am paying you at least 1 year worth of my salary you deserve it.
Pay up dude
I am organic chemistry tutor. You can pay me. I will post my cash app in a few days. Thank you. 🙏🏾
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Can you please post a video for alkyne reactions with hbr and ROOR?
Wow explained nicely thanks
Suggestion for A video; please make chemistry videos from the syllabus of IIT JAM exam.. One of the toughest exams in India.. Please..
What would be the mechanism for
2H-Br + H202 -> Br2 + 2H20 ? If the solvent is ethanol
Ty ...now this topic is as clear as glass for me 😁😁
I've heard that the HBr/ROOR reaction only works for HBr but not other hydrohalic acids. Is this true? If so why?
this is due to the fact that the HCl bond is too strong to be broken to produce free radicals ( bond energy is 430.5 KJ/mol) while the bond energy of the HBr bond is 363.7 KJ/mol.
In case of HI, although the H-I bond is broken pretty easily via homolysis, the iodine atoms so produced immediately react to form iodine molecules instead of attacking the double bond of the carbon atoms in alkene.
well explained bro
thank you for these videoss
I'm that one dude in my class who likes Org Chem....
Wowww❤️❤️
@Organic Chemistry Tutor, is there not an enantiomeric mixture when alkenes reacts with peroxides just as there was with HBr.
Hi guys
Sir you are explaining about morkonia and anti morkania rule
Markovnikov and anti-Markovnikov rules and yes, the more substituted / less hydrogenated carbon gets the Halogen in Markovnikov fashion ( not in presence of peroxide’s ROOR )
I want you tobe my sensei @@##😊😊😊
Why doesn’t RO-Br form ? 5:37
Because we want Br• radical for our next step, where it attacks the alkene. Some of the R-O• and some of the Br• do combine to form R-O-Br, but that is not required for us at the moment for the reaction. Hope it helped