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, , C 60
2. (metal carbide) Ca 2 C, Mg 2 C
3. CO, CO 2
4. (carbonic acid, bicarbonate salt, carbonate salt)
H 2 CO 3 , NaHCO 3 , CaCO 3
5. cyanide, cyanate thiocyanate KCN, NaOCN, NH 4 SCN
H H H H
H C C C C X
H H H H
residue functional
groupgroup
functional group
1. Hydrocarbon
1.1. Alkane
1.2 Alkene
1.3 Alkyne
1.4 Benzene aryl group
2. Alcohol ROH hydroxyl group
3. Ether ROR oxy group
4. Amine RNH 2 amino group
5. Carboxylic acid RCOOH carboxylic group
6. Ester RCOOR oxycarbonyl group
7. Amide RCONH 2 amide group
8. Aldehyde RCHO carboxaldehyde group
9. Ketone RCOR carbonyl group
10. Alkyl Halides R-X ( X F, Cl, Br, I)
1
Isomerism
(Isomerism)
(Isomer)
1.
2.
Double bond equivalent (DBE)
degree of unsatturation
H X N
DBE = C + +1
2 2 2
1DBE 1 1
3
1. : amide > carboxylic > alcohol > amine
2
Alkane C n H2n+2 -ane
1.
Alkene C n H2n -ene
2. KMnO 4
1.
Alkyne C n H2n-2 -yne
2. KMnO 4
MnO 2
Cyclolkyne - Alkyne Cyclo- -yne Alkene
Aromatic Ar- -
3
//
1.
(alcohols) (hydroxyl) 2.
ol
R-OH (Na)
1.
2.
3. Na NaHCO 3
(carboxylic
(carboxyl)
acid) - oic acid
R-COOH
4. (Esterification)
1.
alkyl
2.
(ester) (oxycarboxyl)
R-COO-R
oate
alkyl
(ether) (oxy)
R-O-R - ether
1.
alkane
(aldehyde) (carboxaldehyde) Cu 2 O
e
R-CO-H 2.
- al
4
alkane
(ketone) (carbonyl)
e
R-CO-R
- one
1.
amino
2. ( )
(amino)
(amine) R--NH2
3.
1.
(amide) 2.
oic acid
(amide) R-CONRR
3.
amide
1.
1
1.
2.
3.
4.
5
2. C 3 H 6 O Na
1. 2 2. 3 3. 4 4. 5
3. Br 2 Br 2
UV
1. 2.
3. 4.
4.
1. NaHCO 3
2. NaHCO 3
3. Na
4. 1
5.
NaHCO 3 Na NaOH() Br 2 CCl 4
()
A CO 2 H 2 Br 2
B CO 2 H 2
C CO 2 H 2
D CO 2 H 2
A B C D
1. Cyclohexane Propanoic acid Ethanol Methyl ethanoate
2. Cyclohexane Propanol Ethane Propene
6
3. Hexanoic acid Propane Ethanoic acid Propanol
4. Hexanol Propene Ethyl acetate Propanoic acid