Reaction 6 : Alkene - Alkane
↑ Th
H C C C=
G H H Cataly
-
-
- -
+ -
H H
(Addition : Hydrogenation) (Catalyst : Platinum (Pt) nickel (Ni) Palladium (Pd) +
, NonPolar a
Reaction 8: Haloalkane + Alkene Reaction IO : Alkeney Halo alkane
↑+
cei +KOt3 C H- -
H -
C C= C +
-
Br-Br & Be
· Nal
-
-H = ++
Hi
(Addition : Halogenation)(diotomic
X)
i HH I
O
Z cl C-C-C
- -
=" -
H + He
Reaction 7 : Alhare - Altere
↓ ↓ li
· Thermal Cracking
· CatalyticCracking
-
high temp/high pressure Low
Celimination : Dettydrottalogenation) (concentrated NaoH/(OH)
-
temp/low pressure
-
no catalyst -
Catalyst
↑ 4 H H Reaction 11 : Alcohol Carboxylic acid yester
-
+
He c
-
C -
C-C-C-
11 I
He
Q
I
H H H H H
HH ↑ i I
HH
"T +<C
He
↳
+
H H H -
Cx -
0 -
H + - -
(c -
0 -
2 c - -
H
(
H H H HH H
i
↑
Cesterification) (Sulphuric acid + Catalyst)
Reaction 9 : Alkene Halakene Reaction 12 : Alhane + 02 -
> CO2 + Hz0
Hi C=
M
Hit
E H S4H10 (02 + 5H20
+
H + 02 +
i ci H
Addition : Hydrohalogenation) (Arhydrous +x) 2(4H10 + 1304 + 8 C02 + 10 H 0
,
(combustion)
↑ Th
H C C C=
G H H Cataly
-
-
- -
+ -
H H
(Addition : Hydrogenation) (Catalyst : Platinum (Pt) nickel (Ni) Palladium (Pd) +
, NonPolar a
Reaction 8: Haloalkane + Alkene Reaction IO : Alkeney Halo alkane
↑+
cei +KOt3 C H- -
H -
C C= C +
-
Br-Br & Be
· Nal
-
-H = ++
Hi
(Addition : Halogenation)(diotomic
X)
i HH I
O
Z cl C-C-C
- -
=" -
H + He
Reaction 7 : Alhare - Altere
↓ ↓ li
· Thermal Cracking
· CatalyticCracking
-
high temp/high pressure Low
Celimination : Dettydrottalogenation) (concentrated NaoH/(OH)
-
temp/low pressure
-
no catalyst -
Catalyst
↑ 4 H H Reaction 11 : Alcohol Carboxylic acid yester
-
+
He c
-
C -
C-C-C-
11 I
He
Q
I
H H H H H
HH ↑ i I
HH
"T +<C
He
↳
+
H H H -
Cx -
0 -
H + - -
(c -
0 -
2 c - -
H
(
H H H HH H
i
↑
Cesterification) (Sulphuric acid + Catalyst)
Reaction 9 : Alkene Halakene Reaction 12 : Alhane + 02 -
> CO2 + Hz0
Hi C=
M
Hit
E H S4H10 (02 + 5H20
+
H + 02 +
i ci H
Addition : Hydrohalogenation) (Arhydrous +x) 2(4H10 + 1304 + 8 C02 + 10 H 0
,
(combustion)
