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- Molecule 3 was prepared via molecules 1 and 2. Provide a complete curved arrow mechanism for the most straightforward conversion to 3. You can use HA as your acid and A- as your base.a) Provide a complete detailed mechanism (arrow pushing must be shown) b) If Benzenethiol is used in lieu of 2-Pryidemthiol, the conversion is much less effective. Explain those observations.Give the complete mechanism with arrows and the molecules below.
- Write a reasonable mechanism for the following transformation.Provide a detailed mechanism for the following (Hint:halohydrin reaction). Use arrows to show electron flow and show intermediates.Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Arrange the intermediates below in order of increasing basicity:
- Provide a detailed step-wise mechanism for the following reaction. Be sure to show all intermediates, formal charges, and show the movement of electrons with curved arrows.Provide a reasonable mechanism, including all curvy arrows and intermediates, for the following transformationConsider the following transformation below, which Prof. Ingoglia conducted during his post-doctoral research. a. Draw the product of the reaction in the box provided. b. Provide an arrow-pushing mechanism for the formation of the product you drew in part (a).