I think that there is a chiral centers at $C_2$ and at $C_3$ (Numbering starting such that the carbon with hydroxy attached is number 2.
Then, for $C_2$:
- Priority would be: OH > $C_3$ > $C_1$ > H
- This makes it clockwise, so R
Then, for for $C_2$:
- Priority would be: Cl > $C_2$ > $C_4$ > H
- This makes it anticlock wise, so S
Therefore, the molecule becomes 2R, 3S 3-Chloro-2-pentanol.
Is this correct?
