Draw the most stable form of the major mixed Claisen product formed in the following reaction.
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Question “Draw the most stable form of the major mixed Claisen product formed in the following reaction.”
Draw The Most Stable Form Of The Major Mixed Claisen Product Formed In The Following Reaction.
Answer
The mixed Claisen condensation is performed with two esters. The primary product must be delivered. Claisen condensation occurs in the presence of sodium ethoxide. This causes the formation of .
Claisen condensation refers to a reaction between two esters that have a hydrogen and a base. The $math_tag_0 final product is
$math_tag_0 base abstracts
This is how the carbanion was formed:
Extracting more acidic
This is the mechanism:
The carbanion attacks the carbonyl carbon in ethyl Isobutyrate.
The nucleophilic compound, carbanion, formed in step 1, attacks the electrophilic carbon ethyl Isobutyrate. This intermediate is described below.
This is the final product:
The given reaction produces the primary product as follows:
To form b ketoester, the ethoxide ions are eliminated.
The given reaction produces the primary product as follows:
Conclusion
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