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- A common method where one alkyl halide is converted to another alkyl halide is known as Finkelstein reaction. In one example of this reaction the reaction of an alkyl chloride with potassium iodide is generally carry out in acetone to maximize the amount of alkyl iodine that this formed. Why does the solvent increase the amount of alkyl iodide. Hint: potassium idioide is soluble in acetone but potassium chloride is not.Give a mechanism for the first step of the reaction and explain why it goes in the direction it does.Explain how this occurred under mildly acidic conditions with a full mechanism.
- You were told that is best to use a methyl halide or a primary alkyl halide for the reaction of an acetylide ion with an alkyl halide. Explain why this is so.provide a mechanism for these reactionsGive the reaction mechanism for ETHYNE and bromine solution. Draw and explain the steps of the reaction mechanism.
- a) Free radical bromination is more selective than free radical chlorination. Draw a reaction coordinate diagram for the specific step in the radical chain mechanism that illustrates the source of this selectivity, and explain your reasoning. b) Explain why the bond dissociate energy (BDE) of tert-butane is 95 kcal/mol while the BDE for propane is 99 kcal/mol.Write the reagent and explain the synthesis. Also do the mechanism with explaintion in details.Write the synthesis steps of the reaction given below.
- discuss the generic mechanism of this reaction below . Also explain why this reaction would not proceed if a base was used rather than sulfuric acid. Also What is the purpose of sulfuric acidThis reaction does not follow the expected theory. Given what you know about substitution/elimination, what is the expected mechanism this reaction should follow? Suggest why that is not what happens and give the actual product of the reaction. Br ткон sWhy is it difficult to stop the reaction at the mono-brominated stage?