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AROMATICITY

PERI CYCLIC

PHOTOCHEMISTRY
Federer
Attar
Borman

Benz yne
-7
:
graft up
Bespattered
-
shield

Notes
Diatroppiio

Paratroop ic
mi 2 axis
( M - i )
°

; # ?
• Non
benzoid?
-

\
"
3



cz

• n -
\ =z0&&

resonance
@
@ to
draw
structured .

Bmportant

÷
@
••
FROST DIAGRAM
mm
÷ System having even no :

of
carbon atom

No Anti Mio
No
of
Mo :
bonding
.

of
: =

bonding

odd carbon atom


:
System having
no :
of

€#

:
Case 1
( 4n+3 )
M
anti 0
bonding no >
bonding
.

cation
Eg :
cyclopropane
Case z
: ( 4h ts
)
Mo > Anti Mro
Bonding bonding
-

:
÷

Eg :
Cyclopentyl .

: '

*
Tg=fAROMATlCCoMpound_
WIMP
Cz anis


E
T
*
'



ebook
bonds ) 4 n -1 odd
of
= =
no : A ( n
,

Xd8§ .

an

tautomerisatim
Valency

1€
sked
:#
# /

Aromatic
.

g¥ .
.

Substitution
.
*
Mgm
08 raw
main
-
HO
an
.

Anh
non
not
i ) non -

beryoid odd
iii )n=6 ,n l=
-

ii ) ✓
cz
non - aromatic !

* *

*
# NON AROMATIC
aromatic than @

@ is more

0
@
:.

2*0 \ -
aromatic
Super

e@@
:D
a
E

: :otanheownicted '
.

EIIIEI
*E¥¥
, ...

Anti . aromatic
had assumed It is non alomaticq
A. c
-
H
/

make
Formic acid
Is more acidic
than Phcooh

3. 5 > 4 z
p
.

Ka

.
'
#"
stab

freaking
÷
Note
pg#µ¥ Aromatic
:
!

e-
may
not be effective
Counting A

always

Eooltroo
Acenapnthylene

art to
:
Annotation [Ftne°!FntagYaFagna|
Effect :
12

-
y Nz
- 10

NGU .

Only for
homo
cyclic
compounds . .

Not hetr .
EXCEPTIONS

Aromatic Compounds

initio
:#

:
: a

Kite

ED
Intl
*
it
.

II. E⇒.
Sydn one

Azonein
6
Cz

it:
:

±
E- -

O••0••O
New !
*
PHOTOCHEMISTRY

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