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CnH
2
n
unsaturated
ALKENE
have double
,
hydrocarbon
bonds, C=C where n = 2, 3, 4...
Naming for
alkenes:
-ane change to
-ene
Melting/boiling point:
low
Density:
less dense than water
combustion
reaction
addition
Complete combustion
Product- CO
2
and H
2
O
Example: Butene (C
4
H
8
In an addition reaction:
i) a molecule is
added
to the two carbons of a double bond.
ii) One of the bonds that are part of the double bond
between the carbons, C is broken.
iii) The product is
(1)
ADDITION OF
saturated
HYDROGEN
GAS, H
compound (alkane).
2
(Hydrogenation)
catalysts used: platinum,
Pt
and nickel,
Ni
heated at
180C
Hydrogen molecule, H
2
temperature
150C to 180C
catalyst
C
(Ethene)
(Ethane)
REMEMBER:
Hydrogenation = adding of hydrogen, H
2
and bromine, Br
2
.
The halogen molecule added to the alkene molecule. The product is a
haloalkane
.
Example: X X
||
~C=C~ + XX ~C
C~
Chlorine
H H Propene
H (C
HHH
1,2dichloropropane
(Cl
| | | | | |3
2
H
)
(a) HC=CCH
+
ClCl
HCCCH
6
|||| )
H Cl Cl H
PO
4
.
Heated at:
300C
, under
60 atm
pressure.
Water molecule is added to the alkene molecule. Product is
alcohol
.
Example:
Pentene + Water Pentanol
HHHHHHHHHH
||||||||||
HC=CCCCH
+
HOH HCCCCCH
SO
4
at room condition.
The
purple color
of KMnO
4
is
decolourized
.
The product is an
alcohol
(contain ~two OHdiol)
Example:
HHHHHH
||||||
HC=CCH
~C=C~ ~{~CC~}~
n
||
HH
alkene
polymer
CC=CC
Step 1: Focus to double bonds and bend the other
carbon atom
C=C
||
CC
Step 2: Break the double bonds
~CC~
||
CC
Step 3: Make a bracket between the monomer and
put n.
~{~CC~}~
{||}
{ H H }n
Step 4: Complete the hydrogen atoms
{HH}
{||}
~{~CC~}~
{||}
{CH3 CH3}n