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Why dehydration of alcohol takes place i...

Why dehydration of alcohol takes place in acidic medium generally but not in basic medium

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### Step-by-Step Solution: 1. **Understanding Dehydration of Alcohols**: Dehydration of alcohols refers to the elimination of water (H₂O) from alcohols to form alkenes. This reaction is crucial in organic chemistry for synthesizing alkenes from alcohols. 2. **Role of Medium in Dehydration**: The medium in which the dehydration reaction occurs significantly influences the reaction pathway and the efficiency of the reaction. 3. **Acidic Medium**: - In an acidic medium, the alcohol (R-OH) can protonate the hydroxyl group (-OH) due to the presence of H⁺ ions. - This protonation converts the -OH group into -OH₂⁺ (water), which is a much better leaving group than -OH. - The reaction proceeds with the loss of water (H₂O) from the protonated alcohol, leading to the formation of a carbocation intermediate, which can then lose a proton to form an alkene. 4. **Basic Medium**: - In a basic medium, the hydroxide ion (OH⁻) is present. - OH⁻ is a poor leaving group compared to water. When dehydration occurs in a basic medium, the -OH group does not protonate and remains as -OH. - As a result, the reaction does not proceed efficiently because the -OH group cannot easily leave, preventing the formation of the carbocation and subsequently the alkene. 5. **Conclusion**: - Dehydration of alcohols occurs more readily in acidic conditions because the protonation of the hydroxyl group enhances the leaving ability, allowing the reaction to proceed. - In contrast, in basic conditions, the presence of OH⁻ hinders the reaction due to its poor leaving group ability. ### Summary: Dehydration of alcohols takes place in acidic medium because the -OH group can be converted to a better leaving group (H₂O) through protonation, while in basic medium, the -OH group remains and is a poor leaving group, thus inhibiting the reaction. ---
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RESONANCE ENGLISH-ORGANIC REACTION MECHANISMS-IV-APSP PART-3
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  9. Which one of the following hyxachlorocyclohexane is least reactive and...

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