Chapter 3: Problem 139
(a) phenyl benzoate (b) phenolphthalein (c) Fluorescein (d) \(\mathrm{p}\) -hydroxyazobenzene
Chapter 3: Problem 139
(a) phenyl benzoate (b) phenolphthalein (c) Fluorescein (d) \(\mathrm{p}\) -hydroxyazobenzene
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Get started for freePhenol + phthalic anhydride \(\frac{\text { conc. } \mathrm{H}_{2} \mathrm{SO}_{4}}{\text { heat }}{\longrightarrow}(\mathrm{X})\). The product \((\mathrm{X})\) is used as (a) an antipyretic (b) a catalyst (c) an indicator (d) a laboratory reagent
When phenol reacts with diazomethane \(\left(\mathrm{CH}_{2} \mathrm{~N}_{2}\right)\), the products formed are
The carboxyl group is displaced when salicylic acid undergoes (a) bromination (b) nitration (c) either (a) or (b) (d) dehydration
Mononitration of biphenyl by treating with nitrating mixture gives mainly
Identify the wrong statement. (a) Phenols are stronger acids than alcohols, but weaker than carboxylic acids (b) Phenols, being stronger acids, are soluble in aqueous \(\mathrm{NaOH}\) solution and in saturated \(\mathrm{NaHCO}_{3}\) solution. (c) Phenols are acidic because of resonance stabilization of the phenoxide ion formed by ionization. (d) The \(\mathrm{pK}_{\mathrm{a}}\) of phenol is about \(10 .\)
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