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propan-1-ol 2-bromopropane
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benzene phenylamine
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ethane ethylamine
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phenylmethanol methylbenzoate
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bromomethane ethylamine
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phenylamine N-(4-nitrophenyl)ethanamide
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propene propanone
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ethanol ethane-1,2-diol
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propan-1-ol 2-bromopropane
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benzene phenylamine
•
ethane ethylamine
•
phenylmethanol methylbenzoate
•
bromomethane ethylamine
•
phenylamine N-(4-nitrophenyl)ethanamide
•
propene propanone
•
ethanol ethane-1,2-diol
•
propan-1-ol 2-bromopropane
•
benzene phenylamine
•
ethane ethylamine
•
phenylmethanol methylbenzoate
•
bromomethane ethylamine
•
phenylamine N-(4-nitrophenyl)ethanamide
•
propene propanone
•
ethanol ethane-1,2-diol
•
propan-1-ol 2-bromopropane
•
benzene phenylamine
•
ethane ethylamine
•
phenylmethanol methylbenzoate
•
bromomethane ethylamine
•
phenylamine N-(4-nitrophenyl)ethanamide
•
propene propanone
•
ethanol ethane-1,2-diol
•
phenylmethanol methylbenzoate
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oxidation to benzoic acid (benzenecarboxylic acid) with K2Cr2O7/H+ and reflux, then esterification using CH3OH with conc. H2SO4 and reflux
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phenylamine N-(4-nitrophenyl)ethanamide
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acylation (nucleophilic addition-elimination) with CH3COCl to make N-phenylamide (remember that acylation with amines makes N-substituted amides), then nitration (electrophilic substitution) with conc. H2SO4 and conc. HNO3
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ethanol ethane-1,2-diol
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dehydration to ethene with conc. H2SO4 and reflux, then electrophilic addition with Br2 to make 1,2-dibromoethane, then reflux with NaOH (nucleophilic substition) to substitute both bromine atoms for OH groups
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phenylmethanol methylbenzoate
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oxidation to benzoic acid (benzenecarboxylic acid) with K2Cr2O7/H+ and reflux, then esterification using CH3OH with conc. H2SO4 and reflux
•
phenylamine N-(4-nitrophenyl)ethanamide
•
acylation (nucleophilic addition-elimination) with CH3COCl to make N-phenylamide (remember that acylation with amines makes N-substituted amides), then nitration (electrophilic substitution) with conc. H2SO4 and conc. HNO3
•
ethanol ethane-1,2-diol
•
dehydration to ethene with conc. H2SO4 and reflux, then electrophilic addition with Br2 to make 1,2-dibromoethane, then reflux with NaOH (nucleophilic substition) to substitute both bromine atoms for OH groups
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