1)Describe how the following compounds could be prepared from cyclohexanone using an enamine intermediate (show reaction and all reagents and product)
2)How could 4-methyl-3-hexanone be prepared from a ketone containing no more than six carbons (show reaction and all reagents and products)?
3)How could you prepare the following compound using a starting material that contains no more than three carbons (show reaction and all reagents and products)?