The correct answer is (a) Primary amines alkylated with 1-iodododecane and 4(5)-chloromethylimidazole
Explanation: Polyethyleneimine is formed by polymerizing ethylenemine to give a highly branched hydrophilic three-dimensional matrix out of which 25% of the resultant amines are primary, 50% secondary and 25% tertiary. If 40% of the primary amines may be alkylated with 1-iodododecane to give hydrophobic binding sites and the remainder is alkylated with 4(5)-chloromethylimidazole to give general acid-base catalytic sites. Thus, the resultant synzyme has 27% of the activity of α-chymotrypsin against 4-nitrophenyl esters and it has very low esterase specificity.