Saturday, 18 January 2014

oxymercuration reaction ---- an animation video


oxymercuration reaction

you tube url : http://youtu.be/u4v9GPYhPYE

Oxymercuration is a special electrophilic addition

The oxymercuration reaction is an electrophilic 

addition organic reactionthat transforms an alkene into a 
neutral alcohol.

 In oxymercuration, the alkene reacts with mercuric acetate (AcO–Hg–OAc) in aqueous solution to yield the 
addition of an acetoxymercuri (HgOAc) group and a hydroxy

 (OH) group across the double bond.

 Carbocations are not formed in this process and thus rearrangements are not observed.

 The reaction follows Markovnikov's rule (the hydroxy group 
will always be added to the more substituted carbon) and it

 is an anti addition (the two groups will be trans to each 

other)

. It is anti-stereospecific and regioselective. Regioselectivity 

is a process in which the substituents choses one direction it

 prefers to be attached to over all the other possible 

directions. The good thing about this reaction is that there are no carbocation rearrangement.

http://youtu.be/u4v9GPYhPYE

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