ORGANIC CHE MISTRY
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polythene
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toddy C =L Nickel H H
⑤
H
f- c- c- H condensation
-
catalyst
" H H
A IK9M @
hydrolysis
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> polymerisation
Iropnilic free radical substitution H
bromoptropane
nig
H t
*ogeitUV light 2-
Athene """"¥i%HaI0AI Kane
inzmoieiuies
y
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H -
i. e- H %:
I, It hydrogen halide
①
+
Electrophilic addition
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fain(
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refh.tk
/ C
H
H, P04 catalyst
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, µ
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Secondary alcohol
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H
primary
reduction
all hot
H OH
addition
catalytic
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Nucleophilic On
naBHy +
④ Distillation HI, I,
I'
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1%1 mran.mu.
oh,
ICHI Kiko , this 04
µ If p I / @
+
+
Iffy kilrzo , this 04
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Polyester Aldehyde ketone it "
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2x CO0H groups dicnromate fo, ]
ethanol , +
ZX0H groups Kzlrz 0,14504
✓ L
carboxylic acid
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board Into"n%
⑥
"
carboxylate ,
salts Imm¥a%×idt
it +0 tainan etnanoicacid
% % violent reaction
ACYI chloride
¥¥÷¥I¥¥±%det¥¥I
^ ⇐ -
carbonate primary amine
\
' +
c- c ,
-
←
'
O
-
Nat
,
Acid hydrolysis
/
tion
iumetnanoate ne + ammonia
secondary amide
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i
meat
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ii. K
,
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primary amide
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,
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N methyl ethanamide
O CHZCH , it
-
go
-
Alkaline hydrolysis ( saponification) H C c
ethylpwpanoate
- -
+ OH can
-
' '
H NH ,
heat under reflux
ethan amide
MECHANISMS
1- mechanism
for electrophilic addition for an athene 't
hydrogen halide
2- mechanism
for electrophilic addition for an alkene + halogen 6- Mechanism of nucleophilic addition -
elimination
3- mechanism for nucleophilic substitution
for hydrolysis otahaloalkane Using NQ0H
4- mechanism addition to carbonyl compounds
for nucleophilic ,
↳
tNaBH4 /-
benzene 1
electrophilic
substitution
-
capbonyt.nu/eophiIi additi#
↳ haloalkane -_
nucleophilic substitution
+
NACNIHT
5- mechanism alkene -_
electrophilic addition
for free radical substitution - initiation , propagation '- termination