WebSalicylamide (o-hydroxybenzamide or amide of salicyl) is a non-prescription drug with analgesic and antipyretic properties. Its medicinal uses are similar to those of aspirin. Salicylamide is used in combination with both aspirin and caffeine in the over-the-counter pain remedy PainAid. It was also an ingredient in the over-the-counter pain remedy BC … Weblab iodination of salicylamide abstract the aim of this experiment was the iodination of salicylamide performing an electrophilic aromatic substitution Skip to document Ask an Expert Sign inRegister Sign inRegister Home Ask an ExpertNew My Library Discovery Institutions University of the People University of Georgia
Iodination of Salicylamide : r/chemhelp - Reddit
WebThe mechanism is shown below. ... Discussion In this experiment, the iodination of salicylamide was performed. When this reaction occurs, there can be two possible products. The two products that can form are 2-hydroxy-5-iodobenzamide and … Webmechanism of one reaction; namely, the iodination of phenols in aqueous solutions. Appreciable work on the iodination reaction has been done, and the conclusions concerning the mechanism of the reaction have been several. It has been proposed that the I2 molecule, the I3~ ion, the hypoiodous acid molecule, the I+ ion, or ha sung-woon with you
Salicylamide - Wikipedia
WebThe mechanism of the iodination of salicylamide (with resonance). This problem has been solved! You'll get a detailed solution from a subject matter expert that helps you learn core … WebSalicylamide is the common name for the substance o-hydroxybenzamide, or amide of salicyl. Salicylamide is a non-prescription drug with analgesic and antipyretic properties. It … WebHere is the mechanism of this reaction: The mechanism for iodination is slightly different: iodine (I 2) is treated with an oxidizing agent such as nitric acid to obtain the electrophilic iodine ("I +", probably IONO 2). Other conditions for iodination include I 2, HIO 3, H 2 SO 4, and N-iodosuccinimide, H 2 SO 4. has unh split