The acidities of weak acids. Part IV. Some methyl styryl ketones
Suheila T. Hamdi, John R. Jones, Trevor G. Rumney
Abstract
Suheila T. Hamdi, John R. Jones, Trevor G. Rumney
Abstract
A series of ring-substituted methyl styryl ketones (XC6H4·CH:CH·CO·CH3) have been synthesised and their acidities measured at 298.2 K using solutions of tetramethylammonium hydroxide (0.011 M) in dimethyl sulphoxide–water mixtures. In most cases the rates of detritiation in aqueous hydroxide ion solutions have also been measured. The results show that these compounds obey the same pKa–lgkTOH– relationship as was established for the structurally similar acetophenones.
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A series of ring-substituted methyl styryl ketones (XC6H4·CH:CH·CO·CH3) have been synthesised and their acidities measured at 298.2 K using solutions of tetramethylammonium hydroxide (0.011 M) in dimethyl sulphoxide–water mixtures. In most cases the rates of detritiation in aqueous hydroxide ion solutions have also been measured. The results show that these compounds obey the same pKa–lgkTOH– relationship as was established for the structurally similar acetophenones.
Key concepts: Tetramethylammonium hydroxide, Chemistry, Tetramethylammonium, Hydroxide, Aqueous solution, Ion, Ring (chemistry), Medicinal chemistry