Answer:
See explanation below
Explanation:
You are not providing the alkene you want to stabilize, however, I manage to find a similar question with an alkene. All you have to do is follow the same procedure, cause its pretty similar the steps.
According to the below picture, we have an alkene between carbon 1 and 2, where carbon 2 is less stable than carbon 3 which have another methyl group.
In order to do this, in a first step, the alkene is converted into a alkane by the addition of a hydrogen atom that the hydronium has. Then, in the next step, we have a substraction of the hydrogen in carbon 3 to form the double bond between carbon 1 and 3.
