ORGANIC
Le M IS
MPORTAN TO UNDERSTAND REACTION MECHANISMS BECAUSE
THEY TELL US
WHY And How A REACTION OCCURRED . REACTION MECHANISMS SHOW THE
MECHANISMS Specific and Sequentral MOVEMENT of ELECTRONS
during
A CHEMICAL REACTron This MOVEMENT S
.
REPRESENTED By CURVED ARROWS THAT MUSTRATE
ELECTRON MOVEMEN FROM NUCLEOPAMES TO
ELECTROPHITES .
DENSE MOLECULES WITH ELECTRON RICH ACOMS THE USUALLY HAVE Of
VEOPHMES : ARE ELECTRON IONS OR . ONE OR MORE
The
FOLLOWNG TRLE Bond
A
MEGATE CHARGE
THE CHARACTERESTS A LONE C-C DOUBLE Or To Reactne
.
,
Pors ,
St
ELECTRONS THE BOND HEY ARE NUCLEOPHUES FOR +
k
++
PARTICIPATING
THE ATTRACTED
N .
T CALLED
WAY THEY ARE TO
POSTNELY
S-
NUCLEi
CHARGED
.
ELECTROPHIES ELECTRON ICNS OR MOLECULES W I ELECTRON POOR ACOMS HAVE POSTAE
CHARGE
: POOR A OR
PARTHAL POSTME
THEY
.
DUE TO
DiPOLES CAUSED
By POLAR Bowds
.
T SEE
Exactly How MOLECMES REACT WITH ONE ANOTHER, WE DRAW
ELECTRON MOVEMENT lice How do for Acro-base and resource.
Ayamo
ELECTRONS MOVE NO 3 curved Arrows we
CAN
ONLY WAYS
:
,
H C
Of ELECTRONS
domNG
,
forming
Bond
...
. When A Love par The
Contributes to By : THESE CURVED ARROWS DEPRET THE MOVEMENT A REACTRON
BF3
=
1 > .
H
,
C
H a
,
formation of A NEW Bond n The product
. THERE ARE RULES To Curved Arrows THE HEAd of THE Arrow
DRAWG
.
H HzC
2 Bond WHER A Bond CHX B PONT THE DIRECTION of ELECTRON of
oo
The Reactant MOVEMENT
BrEakmg
MUST THE Arrow
.
=
present N CH Br : 2 : I .
THE TAR
6 o
7
HzC HC
,
BECOMES A LONE OF ELECTRONS THE PRODUCT The ELECTRON Source
AddMrovay Curved Arrows are
Begno
Musy
PANR TN .
& , ,
H
Hay-
It
I
. Bond
3 Bond Bond THE REACTANT SHOW AOM MOVEMENT
A ELECTRON MOVEMENT
THEY
To WHEN NOT USED To
Only
= No
B t
.
2
H
-
It ItzC
is Broken no favour of formaron of a Bord It -
AllyS Pony To ETHER An AcoM Or A Bond, N O MTO
/
EmpTy SpACE .
of Formal
product KEEP
Charges
in the TRACK .
RXN
INTERMOLECULAR REACTIONS : ARE REACTIONS THAT
Types Summary
O COR BETWEEN 2 OR MORE MOLECULES Acid-BASE REACTIONS Addnon REACTIONS - 1 OR 2 STEPS
Br
S
Bi Br
H Br
%. + H +
Nai ↑
- ot
.. >
+ -
② H
7
8+ ↓ O
SUBSTAUTON REACTIONS -1 OR 2
STEPS ELIMINATION REACTIONS - 1 OR 2 STEPS
U Br
& TRAMOLECULAR REACTIONS : ARE REACTIONS THAT
Br +
-
- -
c
+ BrNa" + -
CHz > + Brivat
Nat Nat
Smogle
Occur WITHIN A MOLECULE
o- T
S 3
J ·
+
p Rearrangement
REACTIONS
Off
-
2
Steps
TYPReL INTERMEdrATES :
⑧
O
1 CANTON-HAS An
.
METHYL EMPTY PORBMAL THAT
H
WES
PerpendICULAR TO THE
# t
METHYL PLANE . 2-H Bowds
ARE
Sp3-S OVERLAP .
2
.
METHyL Anton - has a Lone
par no A Sp3
ORBMAL THIS AREA
↑
.
IS
VERY
H H
H
ELECTRON DENSE DUE TO THE
LOVE PAR
Le M IS
MPORTAN TO UNDERSTAND REACTION MECHANISMS BECAUSE
THEY TELL US
WHY And How A REACTION OCCURRED . REACTION MECHANISMS SHOW THE
MECHANISMS Specific and Sequentral MOVEMENT of ELECTRONS
during
A CHEMICAL REACTron This MOVEMENT S
.
REPRESENTED By CURVED ARROWS THAT MUSTRATE
ELECTRON MOVEMEN FROM NUCLEOPAMES TO
ELECTROPHITES .
DENSE MOLECULES WITH ELECTRON RICH ACOMS THE USUALLY HAVE Of
VEOPHMES : ARE ELECTRON IONS OR . ONE OR MORE
The
FOLLOWNG TRLE Bond
A
MEGATE CHARGE
THE CHARACTERESTS A LONE C-C DOUBLE Or To Reactne
.
,
Pors ,
St
ELECTRONS THE BOND HEY ARE NUCLEOPHUES FOR +
k
++
PARTICIPATING
THE ATTRACTED
N .
T CALLED
WAY THEY ARE TO
POSTNELY
S-
NUCLEi
CHARGED
.
ELECTROPHIES ELECTRON ICNS OR MOLECULES W I ELECTRON POOR ACOMS HAVE POSTAE
CHARGE
: POOR A OR
PARTHAL POSTME
THEY
.
DUE TO
DiPOLES CAUSED
By POLAR Bowds
.
T SEE
Exactly How MOLECMES REACT WITH ONE ANOTHER, WE DRAW
ELECTRON MOVEMENT lice How do for Acro-base and resource.
Ayamo
ELECTRONS MOVE NO 3 curved Arrows we
CAN
ONLY WAYS
:
,
H C
Of ELECTRONS
domNG
,
forming
Bond
...
. When A Love par The
Contributes to By : THESE CURVED ARROWS DEPRET THE MOVEMENT A REACTRON
BF3
=
1 > .
H
,
C
H a
,
formation of A NEW Bond n The product
. THERE ARE RULES To Curved Arrows THE HEAd of THE Arrow
DRAWG
.
H HzC
2 Bond WHER A Bond CHX B PONT THE DIRECTION of ELECTRON of
oo
The Reactant MOVEMENT
BrEakmg
MUST THE Arrow
.
=
present N CH Br : 2 : I .
THE TAR
6 o
7
HzC HC
,
BECOMES A LONE OF ELECTRONS THE PRODUCT The ELECTRON Source
AddMrovay Curved Arrows are
Begno
Musy
PANR TN .
& , ,
H
Hay-
It
I
. Bond
3 Bond Bond THE REACTANT SHOW AOM MOVEMENT
A ELECTRON MOVEMENT
THEY
To WHEN NOT USED To
Only
= No
B t
.
2
H
-
It ItzC
is Broken no favour of formaron of a Bord It -
AllyS Pony To ETHER An AcoM Or A Bond, N O MTO
/
EmpTy SpACE .
of Formal
product KEEP
Charges
in the TRACK .
RXN
INTERMOLECULAR REACTIONS : ARE REACTIONS THAT
Types Summary
O COR BETWEEN 2 OR MORE MOLECULES Acid-BASE REACTIONS Addnon REACTIONS - 1 OR 2 STEPS
Br
S
Bi Br
H Br
%. + H +
Nai ↑
- ot
.. >
+ -
② H
7
8+ ↓ O
SUBSTAUTON REACTIONS -1 OR 2
STEPS ELIMINATION REACTIONS - 1 OR 2 STEPS
U Br
& TRAMOLECULAR REACTIONS : ARE REACTIONS THAT
Br +
-
- -
c
+ BrNa" + -
CHz > + Brivat
Nat Nat
Smogle
Occur WITHIN A MOLECULE
o- T
S 3
J ·
+
p Rearrangement
REACTIONS
Off
-
2
Steps
TYPReL INTERMEdrATES :
⑧
O
1 CANTON-HAS An
.
METHYL EMPTY PORBMAL THAT
H
WES
PerpendICULAR TO THE
# t
METHYL PLANE . 2-H Bowds
ARE
Sp3-S OVERLAP .
2
.
METHyL Anton - has a Lone
par no A Sp3
ORBMAL THIS AREA
↑
.
IS
VERY
H H
H
ELECTRON DENSE DUE TO THE
LOVE PAR
