Summary
Notes
term 2
Organic
, Summary notes
Nucleophilic attack
Ni als reaction
formards
↳ ->
mit
Need a strong nucleophile which is a
poor It
so green recution doesn't happen.
i.e need strongly basic vicleophiles, know
this by looking
at pka's.
Organometallics
~organomettalic the
if the seperated then
me-↳x
not
polar aprotic
ether steps are
1 MeLi, THE solvent,
-
0
n-hn
->
2) 120
I
Li-for -> Me-, Lion
second
1
-non be formed
1) LiMe, THF step
will
Liverp e m
basic albosuder im
, Organometallics-> trignard reagents
1)
re
PhMgr, It
*P ->
120 Way to
form a c-c
y
n bond if need to add
Mg to a molecule. Require
phi a c 0
=
group
to attack.
also form Linear, less strichinderance
can acetylide anions ->
but less basic
Buri)
Buli is
basic, oka-so
I
MH ↑ or
n =H is li En
-
H20
↓ ↑
-I
-
~ufon
*-
, THE
form organometallic, metal with the solent, eg
to use
Addition of water ncleophiles to aldehydes and ketones
~"For
Role -
to ->
e -
no
n
on
x
Hydrate
-Br kelones -> disfavour forming catalyst ->
/formaldehyde
hydrate catalyst
without
hydrates
n aldehyde => 50:50 product and reactants
formaldehyde favourable reacts with water
*u very
=> ->
without a catalyst
n
Notes
term 2
Organic
, Summary notes
Nucleophilic attack
Ni als reaction
formards
↳ ->
mit
Need a strong nucleophile which is a
poor It
so green recution doesn't happen.
i.e need strongly basic vicleophiles, know
this by looking
at pka's.
Organometallics
~organomettalic the
if the seperated then
me-↳x
not
polar aprotic
ether steps are
1 MeLi, THE solvent,
-
0
n-hn
->
2) 120
I
Li-for -> Me-, Lion
second
1
-non be formed
1) LiMe, THF step
will
Liverp e m
basic albosuder im
, Organometallics-> trignard reagents
1)
re
PhMgr, It
*P ->
120 Way to
form a c-c
y
n bond if need to add
Mg to a molecule. Require
phi a c 0
=
group
to attack.
also form Linear, less strichinderance
can acetylide anions ->
but less basic
Buri)
Buli is
basic, oka-so
I
MH ↑ or
n =H is li En
-
H20
↓ ↑
-I
-
~ufon
*-
, THE
form organometallic, metal with the solent, eg
to use
Addition of water ncleophiles to aldehydes and ketones
~"For
Role -
to ->
e -
no
n
on
x
Hydrate
-Br kelones -> disfavour forming catalyst ->
/formaldehyde
hydrate catalyst
without
hydrates
n aldehyde => 50:50 product and reactants
formaldehyde favourable reacts with water
*u very
=> ->
without a catalyst
n