illustrate the mechanism of dehydration of 2-methylcyclohexanol, showing how both possible products are formed. Show all electron movement with arrows and include all lone pairs and formal charges.
Draw the E2 mechanism of the reaction between (R)-3-bromo-3-methylheptane and methoxide ion. Show all possible products. Show lone pairs, electron pushing arrows, appropriate stereochemistry, reactants, transition states, and products. Name the product(s). Draw and completely label a reaction energy diagram corresponding to the mechanism you have drawn
1a. Write the complete mechanism for the reaction of 2-bromo-2-methylpentane and KOCH3. If more than one product is formed, you only need to show one mechanistically. Include structure of the reactants, all charges, arrows to show movement of all electron pairs, and ALL products. Also, name the mechanism involved in the reaction.
1b. Draw the transition state for this reaction. Show all full and partial bonds, and full/partial charges.
2. Write the complete mechanism for the elimination reaction between 2-bromobutane and methanol. Show all possible products that can be formed. If more than one product is formed, you only need to show one mechanistically. Include structure of the reactants, the reaction intermediate, all charges, arrows to show movement of all electron pairs, and ALL products. Also, name the mechanism involved in the reaction.
