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13. The reaction of 3-methyl-1-phenylbutane with chlorine yields four different monochlorination products via a free radical mechanism. The experimental distribution of these products is given below. Use this information to determine the relative reactivity of the primary, secondary, tertiary and secondary benzylic hydrogens under these reaction conditions. SHOW ALL WORK!!! on a ou on oso ona 66.27% 12.54% 11.01% 10.18% 14. The free radical reaction of chlorine with 1,3-dimethyl cyclohexane yields five different monochlorination products. Draw the structure of each product, and using the relative reactivities 10-1.0, 29=3.8, and 3°-5.5, calculate the expected percent yield for each of the products. SHOW ALL CALCULATIONS!!! ✔ Chine Show Calculations Here

Answer 1

Question 11.

Primary = 10.18/10.18 = 1.00

Secondary = 12.54/10.18 = 1.23

Tertiary = 11.01/10.18 = 1.08

Benzylic = 66.27/10.18 = 6.51