[Lamp_ray30]

I am trying to answer this: "Under experimental conditions favorable to the E2 elimination, what product can be expected from the treatment of (2S,3S)-2-phenyl-3-bromo-3-methylpentane with a strong base?"
I tried using Newman projections like I show in the picture but I obtained two differenti outcomes. Am I using the right method?

[Hunter2]

Draw the right fisher projection.
It's E2 not Sn2 so you will get an alkene no alcohol.