Arrange the events for the hydrolysis of amide bonds by chymotrypsin in their correct order.

1. attack by Ser 195 to give a tetrahedral intermediate
2. protonation by His 57 and release of the free C-terminus of the hydrolyzed bond
3. protonation by His 57 and release of the free N-terminus of the hydrolyzed bond
4. attack by water, leading to formation of a tetrahedral intermediate
5. binding of substrate to properly position the scissile bond for cleavage

a. 5, 1, 3, 4, 2
b. 5,1,2,4,3 5,
c. 1, 3, 2,4 5,
d. 2, 4, 3, 1