11 8
11 8
11 8
8
HYDROCARBONS
n-Butane
n-Hexane
R OH A
Structure of Double Bond
e C C bond o en known as ethylenic double bond, is Dehydrohalogenation of alkyl halides
∆ L
made up of a sigma ( ) bond and a pi ( ) bond. e sigma R Br + KOH al c. →
bond is a strong bond having bond dissociation enthalpy
of about 397 kJ mol–1 while pi bond is a weak bond having Dehalogenation of dihalides
Zn/Cu K
bond dissociation enthalpy of about 284 kJ mol–1. is RCH(Br)CH(Br)R Ethanol,
∆→
is because -bond is formed by head on overlapping of
orbitals while the -bond is formed by lateral or sidewise Partial hydrogenation of alkynes E
overlapping of the orbitals. Since, extent of overlapping is R C C R
H 2 ,Pd/CaCO3
→
(Lindlar's catalyst)
less in case of -bond than -bond, therefore, a -bond is
weaker bond than a -bond. Na/liq. NH N
R C C R (Birch
3
reduction)
→
Chemical Properties
Addition of hydrogen Oxidation
H 2 /Ni, Pt, or Pd alk. KMnO
→ R CH 4
→ RCH CH
523 − 573 K Cold 2
Addition of halogens OH OH
Br /CCl
2 4
→ RCHBrCH2 Br Ozonolysis
Addition of halogen acids O ,Zn/H O
3 2
→ RCHO or R2 CO
HX
( →R CH CH3
X = Br, Cl, I) Polymerisation
X (Markovnikov’s rule) Traces of oxygen
HBr /Peroxide 1500 atm, 473 −673 K
→ R CH2 CH2Br →
Alkene
Alkene
(Anti-Markovnikov’s rule)
Addition of water (hydration) Wacker process
323 K
H O/ H SO HC CH + PdCl + H O→ CH CHO +
2 2 4
→R CH CH3 Ethene Acetaldehyde
OH (Markovnikov’s rule)
Pd + 2HCl
Diels—Alder reaction
Hydroboration – oxidation
B H /H O
2 6 2 2( alk.)
→ RCH 2CH 2 OH
Oxymercuration – demercuration
(CH COO ) Hg / THF
3 2
→ R CH CH3
H O 2
OH
A
L
K Industrial scale
Y
N
E Electric arc, 3270 K
Cuprous acetylide C
(red ppt.)
L
Oxalic acid
N CHO
CHO
Glyoxal
E
ENVIRONMENTAL CHEMISTRY
AIR POLLUTION
It is the addition of undesirable materials into the
atmosphere either due to natural phenomena or due to
human activity on the earth which adversely a ect the
quality of the air and hence, a ects the life on the earth.
(a) (BrCH2)3CCH2CH2C(CH2Br)3
BrCH2 CH2Br
(b)
BrCH2 CH2Br