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Summary Gringard reactions

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Summary of 5 pages for the course Unit 18 - Organic Chemistry III at PEARSON (Gringard reactions)

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  • August 25, 2022
  • 5
  • 2022/2023
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A-level Chemistry - Topic 18C: Organic Synthesis

met% Grignard Reagents
have
inside
them
of

Notes halogen ◦ alkane
(
usually
Br / I )
Grignard are


used to make

c- C bonds Mg
reagent
:



nucleophilic at
conditions :
dry ether ( solvent )

the carbon reflux


unstable
→ made

just before using it Hgv polar covalent bond
though ,
MgBr'e✓en
metal
H -

C
-
I -





it ~
~
Grignard to =c=O
05
methanol reflux reagent
'




reflux
µ
+ At
+
µ
-
'
% '
R
*
8- C in grignard '

H
it ,H °
'


① R' R
'
+
1- 8
'
-



[ in methanol "

f g
OH H -
- -
c.
bond .




µ ,
-
É I -
-
H + Ht H H
'


OH
'
'
"

② add dilute H H R reflux
acid ( reduce
c=o )
.
_
.
-
-




"
if it if H
µ
OH

H -
c- Cdc -
H I c- I R

!
H
-
-
-




it it it Hit r
' '




ñe and
'




all
dry for


, Questions
1. Suggest a two-step synthesis of from using a

Grignard reagent in one of the steps.
Br
' I
→ M9B ' reflux
Mg

+

dry ether .




H
¥
fl

◦ "
Mg Br reflex
c- d- c"
- •



2) ta -


Ht
if I
'
H
,




2. Suggest a two-step synthesis of from using a

Grignard reagent in one of the steps.


it Brt Mg → ' M9 " •

reflex


dry ether .




AMgBr+ ( 0, →
ÉOH
reflex






At


3. Show how pentan-3-ol can be synthesised from propanal and bromoethane using


ÉÉ
Grignard chemistry.
it it
It c- c- Br Mg
→←
Mg Br
-

+
-




ti't It if
" "
it it , it 9 ◦
the

H -



c- c- MgBr +
→ A- c- c- c- It

Hit
,
, •
µ
it f * ; µ
,

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