What's similar about the valence electrons of Carbon and Silicon?
1 answer:
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Answer:
See explanation
Explanation:
The reaction that we are considering here is quite a knotty reaction. It is difficult to decide if the mechanism is actually E1 or E2 since both are equally probable based on the mass of scientific evidence regarding this reaction. However, we can easily assume that the methylenecyclohexane was formed by an E1 mechanism.
Looking at the products, one could convincingly assert that the reaction leading to the formation of the two main products proceeds via an E1 mechanism with the formation of a carbocation intermediate as has been shown in mechanism attached to this answer. Possible rearrangement of the carbocation yields the 3-methylcyclohexene product.
Carbonyl Compounds containing alpha proton readily donates alpha acidic proton when treated with strong Base. In given statement <span>2-phenylacetaldehyde is converted into Enolate and Enolates acts as a nucleophile and attacks carbonyl group of Benzaldehyde. The mechanism of given reaction is as follow, the movement of electrons is shown by RED arrows,</span>
