Asked by Robert hamlin on Sep 27, 2024
Verified
When hexan-1-ol is treated with conc. H2SO4 at moderate temperatures, ________ is formed via a(n) ________ mechanism.
A) di-n-hexyl ether; SN2
B) di-n-hexyl ether; SN1
C) di-n-hexyl ether; E2
D) di-n-propyl ether; E1
E) hex-1-ene; SN1
Hexan-1-ol
An organic alcohol with a six-carbon chain, where the hydroxyl (-OH) group is attached to the first carbon, commonly used in perfumes and flavorings.
Di-n-Hexyl Ether
An organic compound formed by the dehydration of hexanol, resulting in an ether linkage between two hexyl groups.
- Obtain insight into the reaction pathways of ethers, encompassing their formulation and decomposition.
Verified Answer
GT
Gabriela Trejo2 days ago
Final Answer :
A
Explanation :
The correct answer is A) di-n-hexyl ether; SN2. When hexan-1-ol is treated with concentrated sulfuric acid (H2SO4) at moderate temperatures, it undergoes a bimolecular nucleophilic substitution (SN2) mechanism to form di-n-hexyl ether. This process involves the alcohol acting as a nucleophile, attacking another alcohol molecule in the presence of an acid catalyst to form an ether linkage.
Learning Objectives
- Obtain insight into the reaction pathways of ethers, encompassing their formulation and decomposition.
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