Chem 334 - Summer 1998 - Organic Chemistry I
Dr. Carl C. Wamser Dr. Carl C. WamserVollhardt & Schore, pp 101 - 105:
Problems 2c , 3 , 5 , 6 , 8 , 10 , 12 , 14 , 22
1. Hydrogen reacts with chlorine in a free radical chain mechanism to form HCl. Write out a complete mechanism, indicating the initiation, propagation, and termination steps. Calculate H for each of the steps and for the overall reaction.
2. Fluorine is so reactive with alkanes that the rate is explosive and the products show almost no selectivity. Predict the monofluorination products expected from 2-methylpentane. Give their structures, correct IUPAC names, and the expected proportions of each, based on the selectivity data given in Table 3-5 in your text.