Named Reactions
Named Reactions
Named Reactions
ALDOL CONDENSATIDN
delydus Ketons Lentam m ydrge mdnyo l
additien Dase
calldd aldot:
ppoouta
Jhis j lon hiatmal, m ,B wmsaluwautd aldehyde o
htent ishoumed
aldol aoddikn s a Awcten QutueaM moliu
oo Maldihyde" Ketent o u mmoliulu of alslutele
amd oliul of kitan
CHa- -chs
*CHa - -CH du Alkal C-c-
-CH,-ë-cKG cMsC CH--c,
Acetom CM
Lattuon euible.
e
St b, a movms puoton [H) an
lempomnd cuatmg m onolate M.
carluonyl
a molate n adds to tu aneontt
t stap, tu
tanlon o ad molule ocarduonyt aompomd
Prepare
ethaaldakyds
o
CMg-CM cM-cH
Ado
Aldods w 04ny dhgdiatd uth a m g p
teatment wuth olwa ids to hown K,B msalusatd euldeyda
A
cngcncMH
3 yoaony butanak.
Goum Ketol
CH-C - cH2-ë-CM
2 CMg- -cM
: cM--CMg+CH-c-cM cMsC-cM,C
Ch
4
C-C-CH-cMs Chs--Cn,-c
-H2o
N n
s
fncpamal akde tendinmatuen.
CH-CM2 CM D
Ch-CH2-CH
aB aalsald aldkd
henaral
- ,-c-n o
-
o-,-c-n +C,-C,- C--tn
nelal
--h.
C- Ch, -cn CH-ch
C-CM, cn -ch, - , - c -
42 ARA3 3
-h -i- Ch-Ch,-CH =CH-C -Ë-H
e r f ongond, (eh
wsain bydnogu)
d tiwi lp
wiugo Lorbvsapiao Puptien legeth
ud alelo
alolel
d i l u n k isra) wwgounds
Joch
-H
C n , Ch-c-H t3-CH-C
CH- 4+ , CH-CH
CH + Chs CAM-Ch
-c -H
+CMCH
CH-cH =Ci-H
CH-Ch-è-H ca - cnz--H
CM-CH2 - CH C -CHD + C C - C - = C - co
CH CH3
301s2
3)
CLAISEN CONDEN SATION
CH-CH2-COch
wwn ofu.
moculs d ate mdsyo a tondinu alion
uGcien, t calluel (2kto utb
uochon lain en ondons
alien.
Pacduct LA tuor
Roction
Methauum
3tep
thorg uan emond ydrou hhon th t and
melat 9on.
o aM
thy arut
hycruds en
Ch-CM fo-c
CH CH -C- 0-Cn, CH-C -ocM,
-C-CM C oCM
CH-C C-CoU3 CH-C
CM3
B hto stu
M,c Cotborg
ad.
potliman podut
s
31s CANNIZZARO REACTION
4)
n ho wnu ch Loncmiiatzd alkali, aldehyds actoic
owkamung no H mduso lb udaho an
Rudiuttion to yuld a mwniut ahchel and
alt arluenglie acid
t o a ponomg
touuspondmg aluchol
REACTIDN
So'. Na0 HooNa CH OH
HCHO +HCH1d Muhano
dodi uw
fowaldehyd omaa
CooNa
CHO ChOM
Na CN m
alcolrolhorums Bemyo
RLactuo
NaCN
C-
CH OM
Benaaldhgde
2 ydruoy 1,2 diphunyl sthanon
Ro oh cN m Bmoim todubatie
As a ulopile
*Gusod laamig bvroup
3taloi lie u tatbanien (c)
Mehanso
1)Nutleopeiulee addihen a cyaide CCN) th Banpaldhyde.
Goamatiey a Laroammon.
Lendnation Reacon etuun u cabain amd aa SLLod
L
buiyaldohgde
4) ReavLmae mimt oeahon , tomouimg CN oyoup
up usult a
a Benyom
CN
or¢H-Ht QH
+H
CN CN
H+
KLayoaMg
CN H CN H
CN
C c- Benzoin.
H
A N AT H H Rasuamapmunt
CN
PA- PA
Ph-ë-c-Ph
J Benzoin.
.2.
NAMED REACTIONS
)PERKINS cONDENSATIDN
+CH-CD
CHO+ Ciig CooNa
cH =
CH-toon
CH-CD Cunnamc aid
Aomatie
aeie anuydrids
aldthyde
STEP I
STEPT
M,-CO
-0 -cti co
CMa c o
H cH C0 CH-CD
O
-
-
O-9 -0
.
Z
MICHAELL ADDITION REACTIDN
RLactien oM
Na
C -c-R ong duuut addilby
R-CHCH--R H
R-CH
Pheduct
Na
aelvala
Bwwsatwatd Ktons u a stu, m bides uith
MECHANISM
R- Ch-cH- -R
-c
Canboni aud
sep 3: La monus a preton om calpon
adds to B calloon o
Bmsatiuatd
carben'
stup22:
: enolat a poton em khe soluunt
tonpound" 0md carbon obicimb
WITTI REACTION
oa eten with
uh phesphodiom to evm
e encuon o am alnhud
eacthe.
alkune hmoon wiltig
tcam 4ntucdargng e
uatio
ownall and tla
dolle Qondud bnygen
th calvone compomd
dalle Pondid
Cnoup phophudin
CH CH3 +C) P-0
aC-C-cng
,cls
CeMs)P =o
AOmalsc
MECHANISM
3TEP 1
mkeoplu tic Larbeon thyl atlack Lmbenut
o keten. hu muiloplule attack eault n
othe alolebydu
thu hotmatuon pola 9tumediate hnown as tenane
STEP2
etami AoL tons mmemberud wng Drnd
tmanon Puoktunn onygen md phwphorous hot ou a
M-P(on) -
R
CH2
R- R
R
OPCCHs) *