In aldol condenstaion of the synthesis and isolation of trans-p-anisalacetopheno
ID: 546851 • Letter: I
Question
In aldol condenstaion of the synthesis and isolation of trans-p-anisalacetophenone:
Why does the initial beta hydroxy ketone undergo rapid dehydration?
Why does the initial beta hydroxy ketone undergo rapid dehydration?
1. Because the dehydrated product is more stable due to the extended conjugation. 2. Because the dehydrated product is mores stable because it is a solid. 3. Because the dehydrated product is a lot more fun to say. 4. Becuase the dehydrated product is more stable due to the trans product.Explanation / Answer
Ans : 1 (Because the dehydrated product is more stable due to the extended conjugation). Conjugation increases stability increases.
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