AROMATIC 23107t3

HYDROCARBO .is
ÉÉ Benzene

Halo Benzene
Taft
e Br I
X F

If nitrobenzene

if toluene
methyl Benzene

pot phenol

Benzonitoile a
Toft
cyano benzene

It s aniline G
Benzenamine
 It benzaldehyde

1 Benzoic acid
Toy
JEE
02 and

41
212 114 picnic
21416
trinitr phenol

Moffett salicyl aldehyde

ca hydroxy Benzaldehyde

II inn
salicylic acid
arid
2hydroxy Benzoic

Iterations
in ear
tube
Benzene
Acetylen
 alleyne undergo Polymerisation
when
Fe for a
red hot
in presence of
Benzene
type to produce

3
Ctg
CECH II
Ifan mesitylene
propyne
cuz 5 trimeter
benzene

Decarboxylation
we
carboxylic acid
sodium salt of
when
in pretence
undergo decorbxygation
Naoh 16010
of soda time

II Nato
dona Naoh
of Benzene

TI
SHIITE onatnaon
Nazcoz
 From Grignard Reagent
t

141 BI Htt II
Benzene
G R Acidic
hydrogen

is Present in the
Acidic hydrogen
compounds where the
following
is directly connected to
H atom
atom such
more Electronegative
O H and SP hybridited
as F

carbon

1720 I
OF Water

R off Alcohol

of Acid
Rq
 Ammonia
MHz
R
1 amine
Witz
A 2 amine
122nA
He th 4 Acetylene

t l Alleyne
Rez e n

Active metylene groups

ph on phenol

Ea
SP
DI of Heavy water
Br

FIT Bring 4,4119 G R

f Htt

i reaceswin
me
 to produce benzene
2nd dust

Ist Zno t TI
TIM ten
find Benzene
Phenol zinc tide

Im
antedated H PITH
pig HI toy Nat Hdt

Reducing
Agent Hypo 1hpm
B D C
Dibasic acid
Phosphorous
acid

Na tha t
FI
reducing
Agent HH
Ethanol

FromAlfd
no on E FI
 ing
no 1 Et not
I
I H 20

OH
oh 1
1
I
wth
I it

Fit
Ho

It

ton m
I
 IF
i É
II
H mansion
go
Benzene

KIEFT II It
EI

FI genes ahead
FI
Intramolealen Wurtz
Reaction

Frein
Benzene sulphonic arid undergo
of super
hydrolytic in presence
to produce Benzene
heated

11 H2o Hasoyth
Benzene

Atoms
Chain My dad err entre
when Open
hydro
into Aromatic
converted
Pff end of Cray Afo
carbon it
Produce benzene
at sole to

7203 FI
n
I Benzene
Hexane

I EI
Toluene
a Heptane
 xylene
Feo
1 2 dimeter
Benzene
TV
EY on xylene

N
I FI
p xylene

FI
Ethyl
Benzene