Draw the major elimination and substitution products formed in this reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. Ignore any inorganic byproducts. Draw One of .the Major Products H₂O Br + Draw One of the Maior heat Draw One of the Major Products I 1 I
Reactions of Ethers
Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.
Epoxides
Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.
Williamson Ether Synthesis
An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.
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**Organic Chemistry Reaction Analysis**
**Task:**
Draw the major elimination and substitution products formed in this reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers where applicable. Ignore any inorganic byproducts.
**Reaction Details:**
- **Reactant:** A cyclohexane ring with a bromine (Br) substituent.
- **Reagents:** Water (H₂O) and heat.
**Instructions:**
- In the provided boxes, draw one of the major products for each reaction pathway:
- **Elimination Product:** Identify and draw the major product resulting from the elimination reaction.
- **Substitution Product:** Identify and draw the major product resulting from the substitution reaction.
Ensure that your drawings accurately represent the stereochemistry of the products.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F97a0b142-fcf0-4b7b-946c-b5d706c6bb8f%2F0c618fd1-1c1f-4d1a-90a0-11be934651b0%2Fbvx9u2_processed.jpeg&w=3840&q=75)
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