Question 3 please

1. Explain each step in the synthesis and the purification process of the products for both types of SN reactions. 2. Give a detailed reaction mechanism for each chemical reaction in this experiment. 3. Draw and label a reaction coordinate diagram for both types of SN reactions specific for the reactions of this experiment. You must label the starting structures of the initial state, the intermediates, the transition states and the final products as well as the activation energy and proper titles for the graphs and the axes. 4. Why is the product of part B soluble in hexanes but not the starting material 2,5-dimethyl2,5-hexanediol? Explain. Part B: Synthesis of 2,5-Dichloro-2,5-dimethylhexane by an SN1 Reaction Part I: Synthesis of 2,5-Dichloro-2,5-dimethylhexane 1. Add 0.250g of 2,5 -dimethyl-2,5-hexanediol in a 25mL Erlenmeyer flask. 2. Add 2mL of concentrated HCl to the flask and swirl gently for 5 to 10 minutes. 3. Vacuum filter the contents through a Bchner funnel. Rinse the flask with cold water and add the wash to the Bchner funnel to recover as much of the precipitate as possible. 4. Wash the solid with a small volume of water and allow the solid to air-dry for a few days determine its melting point. Submit the product to the demonstrator and calculate the percent yield