Conceptual Checkpoint 21.22 Draw a mechanism of the following process. That is, draw a mechanism showing conversion of the conju
gated, cyclic enone into the acyclic dione: For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do not use abbreviations such as Me or Ph.
1 answer:
Answer: Provided in the explanation segment
Explanation:
In this question, due to the complexity in actually drawing this manually. i have attached an image that shows how this reaction occurs.
The mechanism as can be seen in the question involves an attack of the hydroxide ion which results in the formation of the enolate ion.
From protonation which follows deprotonation, we can see that the molecules give an acyclic di-ketone which is the desrired product.
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Imagine we have <span>mass of solvent 1kg (1000g)
According to that: </span>
= 4.8 mole * 98 g/mole = 470g
m(H2SO4) which is =<span>470g
</span><span>m(solution) = m(H2SO4) + m(solvent) = 470 + 1000 = 1470 g
d(solution) = m(solution) / V(solution) =>
=> 1.249 g/mL = 1470 g / V(solution) =></span>
According to that: </span>
= 4.8 mole * 98 g/mole = 470g
</span><span>m(solution) = m(H2SO4) + m(solvent) = 470 + 1000 = 1470 g
d(solution) = m(solution) / V(solution) =>
=> 1.249 g/mL = 1470 g / V(solution) =></span>