Predict the products from crossed Claisen condensation of the following pairs of esters. Indicate which combinations are poor choices for crossed Claisen condensations.
(a)
(b)
Predict the products from crossed Claisen condensation of the following pairs of esters. Indicate which combinations are poor choices for crossed Claisen condensations.
(a)
(b)
Predict the products from crossed Claisen condensation of the following pairs of esters. Indicate which combinations are poor choices for crossed Claisen condensations.
(c)
(d)
Show how you would use an aldol, Claisen, or another type of condensation to make each compound.
(d)
Write the mechanism for the reaction of a 1,7-diester with an alkoxide ion to form a cyclic b-keto ester.
Draw the products of the following reactions:
d. diethyl 1,2-benzenedicarboxylate + sodium ethoxide: (1) slow addition of ethyl acetate; (2) HCl
Show how crossed Claisen condensations could be used to prepare the following esters.
(a)
Show how crossed Claisen condensations could be used to prepare the following esters.
(b)
Show how Claisen condensations could be used to make the following compounds.
(a)
Show how Claisen condensations could be used to make the following compounds.
(b)
Show how Claisen condensations could be used to make the following compounds.
(c)
Show how Claisen condensations could be used to make the following compounds.
(d)
Predict the products of the following Claisen condensations.
(a)
(b)
There are other condensation reactions similar to the aldol and Claisen condensations:
a. The Perkin condensation is the condensation of an aromatic aldehyde and acetic anhydride. Draw the product obtained from the following Perkin condensation:
What product is obtained when the product of a Knoevenagel condensation is heated in an aqueous acidic solution?
There are other condensation reactions similar to the aldol and Claisen condensations:
c. The Knoevenagel condensation is the condensation of an aldehyde or a ketone that has no a-hydrogens and a compound such as diethyl malonate that has an a-carbon flanked by two electron-withdrawing groups. Draw the product obtained from the following Knoevenagel condensation: