2) Predict the product of the following reaction and provide a step-by-step mechanism for this reaction K2CO3 SN2 reaction Br Hint: potassium carbonate is a non-nucleophilic base
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- One step in the urea cycle for ridding the body of ammonia is the conversion of argininosuccinate to the amino acid arginine plus fumarate. Propose a mechanism for the reaction, and show the structure of arginine.Provide a mechanism for the following isomerization in aqueous acid. Thank you in advance!a. Provide the structure of the hydrate of cyclopentanone. b. Provide the major organic product which results when pentanal is subjected to the following sequence of steps: 1. PhMgBr; 2. H3O+; 3. PCC.
- Enamines formed from the cyclic secondary amine pyrrolidine are important intermediates in the synthesis of 1,5-diketones. (1st pic) On the structures provided below, draw arrows showing electron flow for the reaction mechanism for the acetic acid-catalyzed formation of an enamine from cyclohexanone and pyrrolidine. (2nd pic)1..Suggest mechanisms for the following reactions:The following compound undergoes Benzilic Acid Rearrangementto yield a hydroxyacid salt. Propose a mechanism for the reaction, write the major product, and provide an explanation as to the preference of migration of one R group over the other.
- Provide a mechanism for the decarboxylation reaction below:Synthesize the following compound from benzonitrile (C6H5CN): Please don't provide hand written solution...3. Provide a detailed, stepwise mechanism for the acid-catalyzed reaction of 2-butanone with ethylene glycol (HOCH2CH2OH) to produce an acetal.
- When N-bromosuccinimide is added to hex-1-ene in CCl4 and a sunlamp is shone on themixture, three products result.(a) Give the structures of these three products.(b) Propose a mechanism that accounts for the formation of these three productsPropose a detailed mechanism for the reaction below (in the attached picture), showing the structure of thestable intermediate and using curved arrows to indicate electron flow in each stepPropose a mechanism to account for the following finding: