Module 2 Practice Problems #1 Consider the reaction below to answer the questions 1-3: (Ch.co toron 40C 65% 25% 10 1. When propylbenzene reacts with tert-butylhypochlorite three monochlorinated products are formed in the ratios indicated. Calculate a reactivity order for each type of hydrogen atom in propylbenzene. 2. The reaction of propylbenzene with tert-butylhypochlorite proceeds by a radical substitution pathway. Draw the structure of the radical intermediate leading to each product. 3. Based on your answers to the two questions above explain why (1-chloropropyl) benzene is the major product of this reaction. 4. Write a stepwise mechanism that shows how a very small amount of CH CH CI could form a during the chlorination of CH