2,4-Dimethylpent-2-ene undergoes an electrophilic addition reaction in the presence of HBr to form 2-bromo-2,4-dimethylpentane. Complete the mechanism of this addition and draw the intermediates formed as the reaction proceeds. Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges where needed. Electron flow arrows should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be created.

the answer is in the diagram

Explanation:

when 2,4-dimethylpent-2-ene undergo electrophilic addition reaction in the presence of HBr to form 2-bromo-2,4-dimethylpentane, it firstly lead to an intermediate carbocation

A carbocation can be describe as an organic molecule, which serves as an intermediate, that has a carbon atom bearing a positive charge and three bonds instead of four

it can be observed without changing the identity of the object.

it depends on what substance you're talking about as well as many other factors. in quantum mechanics, the observation of particles affects the observers ability to measure certain properties. for example: you can know the velocity of a particle, but you can't know it's position; or you can know it's position, but not it's velocity. it's like trying to find out where a grain of sand is by throwing other grains of sand at it. once you find out where it is, it's been moved. it's also like trying to find an answer to the question of whether or not a tree falling in a forest makes a sound if nobody is there to hear it. paradoxically, the only way to find out is to be there and hear it.