The first objective of this investigation was to conduct a systematic study into the reactions of chloroketenes with ketene acetals. The second objective was to explore the synthetic utility of these reaction products and offer a rational explanation for these reaction products.

Trihalomethanes such as chloroform, dichlorobromomethane, dibromochloromethane, and bromoform are formed when natural water is chlorinated in water treatment. This investigation explores the use of ozone to remove organic precursors from natural water, thus decreasing trihalomethane formation potential. The data suggest a mechanism involving formation of secondary precursors after prolonged contact with ozone, suggesting that trihalomethane precursors may be minimized by using low doses of ozone and short contact time.

Rules which correlate structure and insecticidal activity of pyrethroids have evolved over the last thirty years from the results obtained in the testing of various synthetic pyrethroids. The major portion of these rules have dealt either with the development of new alcohol moieties or variations in the unsaturated side chain of the cyclopropane ring. There has been very little work done concerning modifications of the cyclopropane ring. This study was initiated to discover the affect of substituting an aziridin ring for the cyclopropane ring found in pyrethroids.