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CHa <4 tH,
on
a Aeorot CS no product F |
Brhusrel never undo oxidation bemuse Ue hes nod AboMA
@Deryouguration of atone :- a
. STK, Aldehyde + Hy |
[a Alcohol » nude + |
&
CHy- caip-0H) 4893 K, Crisctio 4 +1,
2 Alconel CSPK, Kerone
~
ff. CHa-cui-city YEP cay bcs pai,
FE OH
ti 5° Alcohol CoTS45K Aleene +4150 |
5 oH,
I= i3 cu/543) *
ba Cy = c= 04 -W/stK , CHa-C= CHa + 4190
i Cy Ci,
™ Qa Canned hs Pamannnar is-E= Cts 2 cH 7 ¢
-t-cH
chy cy aaynigo ae E
PREPARATION OF ALDEHYDE:
@ From EROM ACID CHLORIDE CROSENMOND REDUCTION! REACTION)
waren Ha qos th pased one exif criertde bn puecence, Pd Supported ux
Bao tm pay purus by ays natn eam dana
Acid chlovide aiken? Reno + Hal
a
Bae ts Pa ane, oe why
&- CH3- b a rea? Cita ne +40
te a CHO
or ” EB es 2 dea
Buran huoide Burraldenyde,
© FROM NITRILES (STEPHEN REACTION)
o Te
R-C=N ia, Roni te, Reo
Mines 2 Ne ae Te eT
Yeuten
Cor ato
0 ae O
Bunnone Burraldehyde
PREPARATION OF WETONES - hie Suni
@EROM ACP CHLORIDES -
ee)
+ ARG —> Cady + pete
tls 4
EU 4 CAT 9 Cdl + Atty Aty-C- ly
CHy—cH,-0-0 ° ‘ }
( Propiony! chalet de)
@ FROM NITRILES LA
-c=N + R- vy Fe te?
GR Cig-ceN + GHs—Mg—Bs —> Cty -Gite
@ ERIEDEL- CRAFTS ACYLATION
Gs -¢
“asda au,
poy Ay
£4. ‘ wstu_, Luigi a
: ae ee A= cy-citg eni—en) DEH cy oy
pont ' J j Es
1® From ester -
8 4 ay i
R-C40-R’ ee ROH + R-O-H
a ;
Ge w
‘ = ttlp—C- Oty te DIMA, Geico + CHy— City
CHH,— tly aS ag 7! SHS ON TE Cama
TRICK #he bond adjauent to C=0 beaks dnd +H is attarned ty cath 4 |
Of the group:
© FROM HYDROCARBONS ~
cb By oxidation of methyl benxene'- °
@ Use of Cherm Chbovie CETARD REACTION)
When Youtene & tieated with Cro, Cl, Ur presence ob hon-polae
Qpluent Uke CS. then dorm a chdintum Comploy, wht
on further dydlroty ets fous Adenyole:
cr CH(OCOH a)» ; ‘ad
C* os, ones ae
ce ra
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