Eston

EA a d catalyzed

EA
strong and
major
Cresonance)
At least 2 steps

Step 1 : HO transfer (open shell forms) NMR

Rds (step that goes

through highest t .
5) detects symmetry
&

Step 2 Complexation :
less
symmetry , more
signals

2-sided
<

attacks identical C and As

groups
·

C stability indistinguishable/equivalent
If a
signal is shared ,
they a re

enhanced by substitution

#I signalX
byhas/pealsCust
He boa
1: 2 :2: 2 : 3
3 0 2010

an
,
open shell
#11.

#che-
resonance can
partially close a shell

more stable CE , faster reaction and selective

more
Naming
·

EA
strong acid var latiers systematic / step-by-step

straight and (H -x) 1. define main

chain-longest continuous a chain

And otalyst
catalyzed if
·

ring , include
Cyclo-

variations in a bonds · Carbons ? 1 : meth 2 : eth 3 : prop U : but S :

pent 6 : nex L : hept 8 : Oct

Identical Ls .
9 non 18 : dec

differentI s but 20
equally stable
ending -
no l bonds : a re I Abond : ene 2A bonds :
gue
·

different Cs and different 28 stability ad distil , tetra etc if there are more
,
groups
- ol
Example ending

-
2 substituents
.

identify n am e and
group

Anything not an H

"Chloro"
X - C
halogen
>
-

mechanism

Che
· R carbon
CHa-Cec-CH3 -
regeneratne
groups "yl" ending
T
>
-

and neutralize
· Carbons +
(meth , eth . )
product y1 ...
etc

CH3--H andCyl
s
·
sopropyl phenyl
Lett .
3 location

number m a i n chain

variationsI n M bonds
"endings" get lowest possible

give lowest at first point of difference

ONE Cresonance)
·
4) final construction

alphabetically list substituents

 ScumRSignaa .
3
3-dibromocyclopent-1-ene
signals

1.*
·
Real and

#
Ch High Duch
it

chiral

diff attatched
C with U .

things

higher priority higher atomic

=

↑ R
⑭
③
S
can be R
(right) or Scleft)

view with 4th behind

priority

right if 1 , 2 , 3
go
clockwise , otherwise , S

·
0
S-methyl-hept
6
yn 3 -
-
- -