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TUPAC
Chlg CHO
Melhanal
etHg-C-H - Ethana al CHycH,GH 5fuopanal
3-&Hogaudaual
Ctig--CH CHO = 3,8dume fryl
loetanal
CH, =H-CHO CHe
Ph-- c4-CHO
-CHD
SPhany' pep 2-eral
cycloperiareeavbal dahy d.
-CHO
), yolo huan caxbaldthyde
CHO
-)
CHO
4-mettasypntan-2-on
Phenyl ethansn.
Cabatophenoru)
Phco h - kungo phunont 3- Hyduosy but anal
(w) 4-Oropartanal Che- C
0- CH, -CH,- CHD
yelapntanant ()
4- Flueo aotophenana.
-coch;
CH, -cH -CH) ),213 puoparu tricauboldehyd
CHOCHO co,hsy
pontan -2-one
CHE CH
17. Hg S04
cr'g
CHla- Ctt, -CE0H t,o CHz-tt3
(a)
Cth- CE0-CH
HCHO (e
CK
-Ctlg
Co-H,) GeHD
CHg CHO
9)
)
(b) Tolutne ui o0tdisnd loy oulg aud
to
avo acotie arkydui'd
Hgo
cH(0 cocHs)h
-CHO
R-c=NH
A=
R-CEN
A=
ROH0
RCHC
*R-C=N 3HOH
Rre-ox
So2,
Rre-OH
K-CH0 NH3
Qlluyl oqanid
kotone
on uith
R-cEN 2g0
CR-N) R-c-oH
R
K-co-R'
B RCHO
HO
Pd-Basly
Gatixan Koch Ran ; 04/o8/2 3
(o-01HCL
(dialkut
Ackylaton)
+CHg C00oy
knggphoners
Ghanieal
uclcghi
tnat c
NO,
to wat plana
ihiy readily joun n-bond itb wstie tnslsns
(nolase rramj Ketor
ÜnoNaAD , thucky dolubility o aldohydo darurgcs
Bin
OR
than that
Sntext
Chuvnleal Porkuiu
dh aldchydt ucl as keont eh
canbongt Cand caxbayl
Hee caukonuyl eaboo s Cenle
)
Kelone i ltas reaclie than aldohyoe
bccauak t
that ch ony ona Subttuunt o aldehyd
tan
eHg-e=0 <
CHa
t Keton
Bngaldlydi
OR
is ows iaclie Han pukanal, why ?
pcjanal , why ?
bungaldthyde chas
diecots the naolecbhilicty caubonyl cabon and hi
,
Mecharium
1) ohowo)
) enp
)A
ddtioo R
1
H
hiyly pulo)
R-C. 9)
P
u)
Jhoo .
cnueao
Cchival)
phunyl2-hydueny cttonauc acid
) engaldehyde to (Máundalie aid)
c-c00H
1
ciHg
to 9-hydsueny-2-phenyl
aeid
projna
C-cN
)
CH3 CH
CN H0
H-c-CN
0.
Ch-tct CH-c-cN CH3-e-cCN
Sow
CtB 1)
(iat ohonce oh s0)
tto CHo
CHO
NO
(-7)
.e daljitint
CHO
CHC- Ce, Hg
CHa Cti
CH
CHg lo Chlg CHz0H
Ct
(kotal)
ktal)
ConuooL CHO
CHO
H0
1
CHO
A=
NaBy
o-CH
cocH3 coCHg
cHO HCNCInoa)
CHO
A9 CH-Chg-CH, e
CIntamoeulo
fudd ba)
CHa
A
allkass
alccho)
Hel to allane
C-Cbt
yR-cH3
A) Oois
ReHO
R- Cth
dlolehy dr & lectene iact
(uith
hiatrig th alliali Co,H 0Na /'Nae/Ko) to gie
allant
R-CHo R-cH3
R-CH3
A
vo H/y
- k
R- C0-R
-Hg.
R CHO
KCHO Ao
ROH Cu,
CHo
iognt
dcu not ordues tollrti iogut
foopa
9lu504
RHO+ 30
-(po
lrqpanal
CiHo 2 ut"o CHO
alo can
)
yoosil Aníns NI,o)
(
1,N NH
NO
(d)
-NO,
) IAnL RNH,
4) Atnonia -NH (2)
uitt
-C0t NOH
kelo mu
6) hycdiasn
hydvngone
R-C =NN H
R-C=0 1, N- N
R-c-R'
(a)
K-C.0 H, NNH c0
C0 NH}Ro=NNH CO Nb2
R-C= NNH
|2) KC=0 t
H
1,N NH
-N
R R
68
kelimine.
41dinine &
E)
as
ldumin s lenoen
A
85
FNOH
-CHO
tæ)
-NNH
)
) Hetir
()
atone
jot
N
68
(4) CH3
-CHO
jalauig
Ny Hy/koH
Dthan al ond
btlnal) 9atlg-ChHo
NaoH di
eCthydvrationpuuct atòneondtns aldol N
giepuodint Fhia .kotol ond aldou
tng atom Ho-haur mose dao ketone &
9 CH2-(tl
-CHO
Ctlg-(0--CH2
acbena!
CH HO HOHO
Ple:
OH 2CHaCHt,
OH
ialde
CHgt Hlg-CH10 CHl- CH, CHO
Aldol =
Ct CH -CH0
CH3
2CH, - CH-CH0
CH-Ctl,- CHO -