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The given diene can undergo ring‑closing metathesis in the presence of a ruthenium catalyst. Draw the expected products.

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Final answer:

The given diene can undergo ring-closing metathesis in the presence of a ruthenium catalyst to form a cyclic compound.

Step-by-step explanation:

The given diene can undergo ring-closing metathesis in the presence of a ruthenium catalyst. In ring-closing metathesis, a double bond in the diene reacts with another double bond to form a cyclic product. The ruthenium catalyst helps facilitate this reaction. The expected product of this reaction is a cyclic compound formed by the closure of the diene. For example, if the diene is butadiene, it can react with another alkene to form a cyclic six-membered compound. The specific products obtained will depend on the structure of the given diene and the alkene it reacts with.

User Ahuva
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Final answer:

The given diene can undergo ring-closing metathesis in the presence of a ruthenium catalyst, forming a cyclic product.

Step-by-step explanation:

The given diene can undergo ring-closing metathesis in the presence of a ruthenium catalyst. In this reaction, the diene reacts with itself to form a cyclic product. The ruthenium catalyst helps facilitate the rearrangement of the double bonds in the diene to form the new cyclic product.

User Sweden Edgar
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