Step #1

• Part #1: Hydroboration of the alkene. In this first step the addittion of the borane to the alkene is initiated and prceeds as a concerted reaction because bond breaking and bond formation occurs at the same time. This part consists of the vacant 2p orbital of the boron electrophile pairing with the electron pair of the ? bondof the nucleophile.

Transition state

* Note that a carbocation is not formed. Therefore, no rearrangement takes place.

• Part #2: The Anti Markovnikov addition of Boron. The boron adds to the less substituted carbon of the alkene, which then places the hydrogen on the more substituted carbon. Both, the boron and the hydrogen add simultaneously on the same face of the double bond (syn addition).

Step #2

• Part #1: the first part of this mechanism deals with the donation of a pair of electrons from the hydrogen peroxide ion. the hydrogen peroxide is the nucleophile in this reaction because it is the electron donor to the newly formed trialkylborane that resulted from hydroboration.

• Part 2: In this second part of the mechanism, a rearrangement of an R group with its pair of bonding electrons to an adjacent oxygen results in the removal of a hydroxide ion.

Two more of these reactions with hydroperoxide will occur in order give a trialkylborate

• Part 3: This is the final part of the Oxidation process. In this part the trialkylborate reacts with aqueous NaOH to give the alcohol and sodium borate.

If you need additional visuals to aid you in understanding the mechanism, click on the outside links provided here that will take you to other pages and media that are very helpful as well.