The correct option is A Tertiary > Secondary > Primary
R−OH+HX→R−X+H2O
When alcohols react with halogen acids, alkyl halides are formed. Generally, reaction takes place via SN1 mechanism.
In the first step protonation of alcohol takes place. In the second step carbocation is formed. In the third step attack of nucleophile occurs.
As we know tertiary carbocation is the most stable followed by secondary and primary carbocation, reactivity order will be in the order tertiary > secondary > primary. Hence, option (a) is correct.