Answer:
Step-by-step explanation:
The reaction is incomplete cause you are not putting the structure. However I manage to find one, and it's in picture 1. In picture 2 you have the whole mechanism.
A claisen reaction involves an ester and an alkoxide base. It could also work with acid, but works better with a base.
This reaction is done in 4 steps. The first step is the formation of the ester enolate. The second step is a nucleophilic adition. The third step is eliminating the etoxide formed. The fourth step is transform the ceto exter in an enolate. and the final step is forming the enolate of the ceto ester.
In the picture below, the second, you can see the whole mechanism and the final product in each step mentioned above. Check it out.