1. C2H5OH
2. C2H5NO2
3. CH3CHO
4. CH3COOH
C2H5OH
1. Aniline
2. Dimethylamine
3. Methylamine
4. Trimethylamine
Dimethylamine
1. renders the ring basic
2. deactivates the ring towards nucleophilic substitution
3. deactivates the ring towards electrophilic substitution
4. activates the ring towards electrophilic substitution
deactivates the ring towards electrophilic substitution
1. (CH3)4N+I-
2. CH3OCH3
3. (CH3)3S+I-
4. (CH3)3CCI
(CH3)4N+I-
1. Sublimation
2. Chromatography
3. Crystallisation
4. Distillation
Distillation
1. Acid
2. Alcohol
3. aldehyde
4. N-oxide
aldehyde
1. Sp
2. Sp2
3. Sp3
4. no hybridization
Sp3
1. Sn/HCI
2. H2/Pd-C
3. Zn/NaOH
4. Zn/NH4CI
Zn/NH4CI
1. from aniline by diazotisation followed by heating the diazonium salt with HBF4
2. by direct fluorination of benzene with F2 gas
3. by reacting bromobenzene with NaF solution
4. by heating phenol with HF and KF
from aniline by diazotisation followed by heating the diazonium salt with HBF4
1. primary aromatic amine
2. Primary aliphatic amine
3. Secondary amine
4. Tertiary amine
Primary aliphatic amine