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benzyl-alcohol react with hcl forms benzyl chloride + MgCH3 nucleophilic substitution follwed by OH- IN ANTI MARKONIKOV RULE GIVES PRODUCT

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12y ago
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4mo ago

Benzyl alcohol can be converted to 2-phenylethanoic acid through oxidation using a strong oxidizing agent such as potassium permanganate (KMnO4) in acidic conditions. The benzyl alcohol is oxidized to benzoic acid, which can then be further oxidized to 2-phenylethanoic acid by using a milder oxidizing agent like Jones reagent (chromic acid).

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Q: How to convert benzyl alcohol to 2-phenylethanoic acid?
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What is the ester formed from benzyl alcohol and acetic acid?

The ester formed from benzyl alcohol and acetic acid is benzyl acetate.


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Benzyl alcohol can react with hydrochloric acid to form benzyl chloride and water in an acid-catalyzed reaction. This reaction is commonly used in organic chemistry for the synthesis of benzyl chloride.


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Benzyl alcohol is an aromatic alcohol commonly used as a solvent, preservative, and flavoring agent. Acetic acid is a clear, colorless liquid with a pungent odor, commonly used in vinegar production, food preservation, and as a solvent. Both compounds have distinct chemical structures and properties, with benzyl alcohol being an alcohol and acetic acid being a carboxylic acid.


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Benzyl acetate is neither an aldehyde nor a ketone. It is an ester, specifically the ester of benzyl alcohol and acetic acid.


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When toluene is treated with alkaline KMnO4, it undergoes oxidation. Toluene is converted to benzyl alcohol, and further oxidation can convert benzyl alcohol to benzoic acid. The purple color of the KMnO4 solution will fade as the reaction proceeds.


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The reaction of benzyl alcohol with sodium metal results in the formation of sodium benzoate through the oxidation of benzyl alcohol to benzoic acid and subsequent reaction with sodium hydroxide. The reaction of glycerol with sodium metal results in the formation of glycerol sodium alkoxide and hydrogen gas through a displacement reaction.