Further Synthetic Routes (OCR A-Level Chemistry A): Quizzes

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Further Synthetic Routes
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Which functional group is represented by \ce−CONH−\ce{-CONH-}?

Amide

What product forms when a haloalkane reacts with \ceNaCN\ce{NaCN} in ethanol?

Nitrile

What is the product of complete oxidation of a primary alcohol using \ceK2Cr2O7/H2SO4\ce{K2Cr2O7/H2SO4} under reflux?

Carboxylic acid

What does an acyl chloride produce when reacted with \ceNH3\ce{NH3}?

Primary amide

What product forms when a nitrile is hydrolysed with \ceH2O/HCl\ce{H2O/HCl}?

Carboxylic acid

Which reagents are required for the nitration of benzene?

Conc. \ceHNO3\ce{HNO3} and conc. \ceH2SO4\ce{H2SO4}

Why does aniline react with \ceBr2(aq)\ce{Br2(aq)} without a catalyst?

\ce−NH2\ce{-NH2} group activates ring strongly

What is the product when phenol reacts with \ceBr2(aq)\ce{Br2(aq)} at room temperature?

2,4,6-tribromophenol

Which group is meta-directing in electrophilic aromatic substitution?

Nitro group (\ce−NO2\ce{-NO2})

Which reagent converts a carboxylic acid to an acyl chloride?

\ceSOCl2\ce{SOCl2}

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