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- Treatment of 1,2-dibromoethane with the dithiolate dianion shown in the reaction below leads to two products as shown. Draw the structure for each molecular formula and provide a detailed mechanism for the formation of both products.The reaction below could run through both substitution and elimination reactions. 1. Provide the correct reagent to produce the products shown 2. State which mechanism(s) was followedFor each reaction, predict what mechanism will account for the major product(s) formed and write (SN1, SN2, or NR) in the boxes provided. Explanations or drawings are not required.
- Predict the product(s) and provide the complete mechanism for each reaction below.Propose 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 mechanisms (SN1/E1) to account for all the products shown in the reaction
- Please provide the major product via an SN2 mechanism. The formula of the final product is C5H11N..In the presence of acid such as H2SO4, 3,4-dimethyl-1-pentene undergoes isomerization to 2,3-dimethyl-2-pentene (shown below). Write a complete mechanism, showing all steps and using curved arrows to explain this observation.Write whether it will be E1, E2, SN1, and/or SN2 Show the mechanism(s) Write the MAJOR product(s) State the stereochemistry of the product(s), when applicable. Please do them in the form provided