Br CH₂ Br H₂O 110 °C a CH₂

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Draw an arrow pushing mechanism for this SN1 reaction
The image depicts a chemical reaction diagram. 

**Reactant Structure:**

- The reactant is a bicyclic compound featuring two benzene rings that share a common bond.
- Two bromine (Br) atoms are attached to the benzene rings, specifically at adjacent positions.
- A methyl group (CH₃) is also attached to one of the benzene rings.

**Reaction Conditions:**

- The reaction takes place in the presence of water (H₂O).
- The temperature specified for the reaction is 110°C.

**Product Structure:**

- The product is another bicyclic compound, where one of the benzene rings now contains an oxygen atom incorporated into a five-membered ring.
- The methyl group (CH₃) remains attached to the original position adjacent to the oxygen atom, indicating the formation of a heterocycle.

The overall transformation implies the conversion of a dibrominated aromatic hydrocarbon to a bicyclic aromatic ether through a high-temperature reaction in the presence of water.
Transcribed Image Text:The image depicts a chemical reaction diagram. **Reactant Structure:** - The reactant is a bicyclic compound featuring two benzene rings that share a common bond. - Two bromine (Br) atoms are attached to the benzene rings, specifically at adjacent positions. - A methyl group (CH₃) is also attached to one of the benzene rings. **Reaction Conditions:** - The reaction takes place in the presence of water (H₂O). - The temperature specified for the reaction is 110°C. **Product Structure:** - The product is another bicyclic compound, where one of the benzene rings now contains an oxygen atom incorporated into a five-membered ring. - The methyl group (CH₃) remains attached to the original position adjacent to the oxygen atom, indicating the formation of a heterocycle. The overall transformation implies the conversion of a dibrominated aromatic hydrocarbon to a bicyclic aromatic ether through a high-temperature reaction in the presence of water.
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