@Oh_Gee
Grignard just makes a strong nucleophile.
In the first reaction, the Grignard attacks (adding methyl group while getting rid of a Cl).
In the second reaction, Oh- attacks (adding OH while getting rid of the second Cl).
The carbon at the center is now bonded to
1) H
2) OH
3) CH3
4) CH3
There are 2 CH3 groups and 1 OH group so that is a secondary alcohol.