SN1 Carbocation Rearrangements - Ring Expansion Problems | Summary and Q&A

TL;DR

Ring expansion reactions occur in alkyl halides, where a smaller ring can expand to form a more stable larger ring.

Key Insights

• 😋 Secondary alkyl halides and protic solvents favor SN1 reactions in ring expansion reactions.
• 😋 Five carbon rings can expand to six carbon rings, which are more stable.
• 😋 Hydride shifts and methyl shifts can occur in ring expansion reactions depending on the adjacent carbons.
• 😋 Tertiary alkyl halides and protic solvents favor S1 reactions in ring expansion reactions.
• 😋 The choice of solvent can impact the type and outcome of ring expansion reactions.
• 😋 Alkyl halides can undergo rearrangement or shifts during the formation of carbocation intermediates in ring expansion reactions.
• 😋 Ring expansion reactions can lead to the formation of more stable and larger ring structures.

Transcript

in this video we're going to cover examples that involve ring expansion so let's say we have this particular alkyl halide and we're going to react it with water what is the major product of this reaction now the first thing we need to do is determine what type of mechanism are we dealing with here sm1 E1 sn2 or E2 so what we have here is a secondar... Read More

Questions & Answers

Q: What determines the type of mechanism in ring expansion reactions?

The type of mechanism in ring expansion reactions is determined by the nature of the alkyl halide and the solvent. Secondary alkyl halides and protic solvents favor SN1 reactions, while tertiary alkyl halides and protic solvents favor S1 reactions.

Q: Why does a five carbon ring expand to a six carbon ring in ring expansion reactions?

Five carbon rings can expand to six carbon rings in ring expansion reactions because the formation of a six carbon ring is more stable. Six carbon rings are highly stable structures, which is why they do not undergo rearrangements.

Q: What happens when a four carbon ring undergoes ring expansion?

When a four carbon ring undergoes ring expansion, it can expand to a five carbon ring. The positive charge is placed on the carbon that has lost the bond to accommodate the expansion.

Q: Can ring expansion reactions occur with other solvents besides water and methanol?

Yes, ring expansion reactions can occur with other solvents as long as they are able to act as nucleophiles or bases. The choice of solvent can affect the type and outcome of the ring expansion reaction.

Summary & Key Takeaways

• Ring expansion reactions involve alkyl halides reacting with water or methanol to form a more stable, larger ring.

• The type of mechanism depends on the nature of the alkyl halide and the solvent used. In the examples provided, the reactions favor SN1 and S1 mechanisms.

• In these reactions, the alkyl halide forms a carbocation intermediate, which can rearrange or undergo shifts before further reactions with water or methanol occur.