Draw the mechanism for the friedel crafts reaction of 4 - phenylbutyric acid to alpha tetralone with methanesulfonic MeSO H 3 acid as the catalyst 85-100® C OH MeSO H 85-100 °C
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- Show how the synthetic scheme developed in Problem 23.67 can be modified to synthesize this triiodobenzoic acid X-ray contrast agent.When 4-dimethylaminopyridine (DMAP) is added in catalytic amounts to acetic anhydride and an alcohol, it significantly increases the rate of ester formation. The process begins with a reaction between acetic anhydride and DMAP to form a highly reactive acetylpyridinium intermediate that is more reactive than acetic anhydride itself. Propose a mechanism for this process that includes the formation and reaction of the acetylpyridinium intermediate.What is the final product
- How is this compound synthesized with its reaction mechanismWhat is the major organic product of the following intramolecular Friedel- Crafts Acylation reaction? - CI AICI వ- డెవదిద్దడ -CI OI 0 1 8 || OIV OV IVIdentify X and Y, two mtamediates m the synthesis of the antidepressant venlafaxme (effexor) m the following reaction scheme.
- The following reaction is: Ph Ph-p-In(CI)(PPH3)2 B-elimination H reductive elimination insertion oxidative addition H Ph₂P- -İn(CI) (PPH3)2 my floreThe following three derivatives of succinimide are anticonvulsants that have found use in the treatment of epilepsy, particularly petit mal seizures. Q. Propose experimental conditions for the conversion of (C) to (D).Steps of mechanism of reaction