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The name of the reaction is aldol condesation (Cl.pdf

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The name of the reaction is aldol condesation (Claisen) (it usesbase to form a enolate and it atacks over the diketone one time andthen it atacks again intramolecular to form the ring), the -OHformed in the condesation are eliminated to form the two doublebonds. The functional group present in the product is a ketone andthe hydroxi groups that were eliminated. Solution The name of the reaction is aldol condesation (Claisen) (it usesbase to form a enolate and it atacks over the diketone one time andthen it atacks again intramolecular to form the ring), the -OHformed in the condesation are eliminated to form the two doublebonds. The functional group present in the product is a ketone andthe hydroxi groups that were eliminated..

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The name of the reaction is aldol condesation (Claisen) (it usesbase to form a enolate and it atacks over the diketone one time andthen it atacks again intramolecular to form the ring), the -OHformed in the condesation are eliminated to form the two doublebonds. The functional group present in the product is a ketone andthe hydroxi groups that were eliminated. Solution The name of the reaction is aldol condesation (Claisen) (it usesbase to form a enolate and it atacks over the diketone one time andthen it atacks again intramolecular to form the ring), the -OHformed in the condesation are eliminated to form the two doublebonds. The functional group present in the product is a ketone andthe hydroxi groups that were eliminated.

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The name of the reaction is aldol condesation (Cl.pdf

  • 1. The name of the reaction is aldol condesation (Claisen) (it usesbase to form a enolate and it atacks over the diketone one time andthen it atacks again intramolecular to form the ring), the -OHformed in the condesation are eliminated to form the two doublebonds. The functional group present in the product is a ketone andthe hydroxi groups that were eliminated. Solution The name of the reaction is aldol condesation (Claisen) (it usesbase to form a enolate and it atacks over the diketone one time andthen it atacks again intramolecular to form the ring), the -OHformed in the condesation are eliminated to form the two doublebonds. The functional group present in the product is a ketone andthe hydroxi groups that were eliminated.