Yes, thats a primary alcohol.
They CAN undergo halogenation, but not via SN1 pathway (which I was assuming what he was asking). Basically what can happen is that the alcohol gets protinated, and then a nucleophile attacks the backside of the carbon atom (relative to the leaving group) and "kicks out" the leaving group, rather than waiting for the carbon to ionize on its own, then attacking the carbocation. This results in a stereochemical inversion of the molecule.
There could be other mechanisms that I'm not aware of yet, I'm only 1/2 way through the first semester of the course.