I think that Dave only showed the reaction occurring at one double bond because the molecule was symmetrical. It would have been the exact same reaction had the reaction taken place at the other double bond.
i think it's pretty safe to say that in general hydrohalogenation is not stereospecific, there may be counterexamples with special catalysts or something but i'm not aware of any such thing.
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Boom. Clear, consistent, concise explanation. Thanks
You need that intro in all your videos! It rocks!
was this the first time???
This guy is a real legend!
Conjugated polyunsaturated systems? More like "Cool videos and lots of students like them." Thanks for making all of them!
you deserve more love
4:15 he knowwwwws we hate it lol
Yeah keepin stuff simple is best.
why the other double bond did not go through addition reaction?
I think that Dave only showed the reaction occurring at one double bond because the molecule was symmetrical. It would have been the exact same reaction had the reaction taken place at the other double bond.
How about 1,4-addition?
Can we say that the addition of H-X on an alkene is not stereospecific in general or is that specific to this case?
i think it's pretty safe to say that in general hydrohalogenation is not stereospecific, there may be counterexamples with special catalysts or something but i'm not aware of any such thing.
Thank you sir
good job thank youu
Good
Sir,Are all the given in the above tutorial products major ??
yep should be a fairly even distribution.
thank u sir
polo
Marco?