I think benzyl alcohol have a CH2 group in between the OH group and benzene so when OH releases a H+ O- formed willnot be much stable as no resonance is going to take place.... so it isnt soluble in NAOH
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Benzyl alcohol can be dissolved in sodium hydroxide with the appropriate conditions. The solubility of benzyl alcohol in sodium hydroxide will depend on factors such as temperature and concentration of both substances.
Benzyl bromide can be converted to benzyl alcohol through a nucleophilic substitution reaction using a strong nucleophile such as sodium hydroxide (NaOH). The reaction involves the attack of the hydroxide ion on the bromine atom of benzyl bromide, resulting in the displacement of bromine and formation of benzyl alcohol. The mechanism typically occurs in a polar solvent like water or alcohol.
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.
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A 3 M sodium hydroxide solution means there are 3 moles of sodium hydroxide dissolved in 1 liter of solution.
The chemical formula for the aqueous solution of sodium hydroxide is NaOH (sodium hydroxide) dissolved in water.