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Chemical Properties of Ald Keto & Carboxylic Acid
Chemical Properties of Ald Keto & Carboxylic Acid
Page No
EXPERIMENT:
Date
b
step2 OH
b
Tetrahedal
Iatamediel Additi Ds Produck
G.RI
why Gre aldehydes rcoctrc ton (cetones
MOe
Nundarem
Teacher's Sign.:
2.
(u HO
(w
H/
+lelket -Iefet
Be0zoldekyde -M eket
p- Touldehyde
p-Nitoben zaldehyde
Aceto phein one <p-Toluei.l dekyde < Benzeldohde
kp.Nitrehenzdl
dehyde.
Page No 3
No.
EXPERIMENT: Date
HO
homno/hCACH
cyanchydrin
exampleb oy
ph a o
Cody
C=otNaHs +Necl ts
Acetaldebyden tieya
NaOH
(P c
Acetone Nabipuhile
asundaram)
Teacher's Sign. :
4.
3) Adtion u G.R: studied in Ale. phenold ethe
No, 323 NcELT
to reMenbe
Thing
duy ethen
Fosmaldehyde t R-Mgx Alcoho)
Mcle)
ethonal ethan|
(Alkoryaletel Acetzjdelydedity
Kcetal
(oy nel protonetes the O-ctog is called Hemiacatei)
eletpliuy e) Cgem-didlkon)
Gcetal
cetone reacto with dihydrie alcch oa to
HO-U d nci
reeoibe.. Acetes
are rereoble
Above ttoreac honsare ketal are
hydydby dil hcl to genenat. the oigihet aldehyde teketons
Ht
C=o t 244goH
Aateikeyèe diettyl acetel Acatal dekyde
Page No 5
No.
EXPERIMENT: Date
H1
AmMoia
Ad/ Keto desvatves Deivetves
-R Amine C=NR
pH3-s
-amine Shanel XÍme
e 1m
asundaram) Teacher's Sign.:
2. Reecton wth hydzine;
Ht
Paopanone hydazone
3. Reacten cwith phaoghydezine:
pH3
Phe ny lhydezine honel phenyhydezine
Paopanone phenythydhazine
4. Reectaon wrth 2, u-
4- dinrtrophenyhy drzine (Bredy's Reaponty
Ht
ph 3
tyo
Similely cit
csith lcetone Gthonel 2-dinitropheyl
5. Reacion coth Semi canbezidei
-Aydazine
Ht
Ethonclseii caubazone
ht
c=o t MwH cONM, 3
ph3 NHeOy t o
Papanone seml canb az0 oe
Page No+
No.
EXPERIMENT: Date
Reduction
RCHO
2° Alcshol
Reductin of conbonyl to tom hy do canbonsi.
a) lembnensen reducon
R- CHo t 4 (u]
cycoen + 4c
Nof- Kishner edu ction;
RH=NNH
hydezne 4s3.4k
2. A
293K
3-Dipheng'prop- 2-en-I-one
CBen 2elacetophenone)
Other reactions:
Connizzaro eacio, Aldehyde cohi h do not ha
2n
an k hydugen ctom, undego self ondetos d
reducton Ldiopro portionat on) reecuon on heatng t
Conc. akeC.
ok
Methane) Potzssi
Cormeldehyde fm
How to wni in ex to remese
othen example,
Ocoa
Benlalustol sod bentoate
Seetrophilic Substution reecon; Catonyl qyp aca aola
deactung L modirecting qp in be electrphilic auomate sut
reactionf f aomete ald. d ket.
eno
nNoglysQ,
223- 2$gK
Comyula kollouing
soH
M-senzal dehyde suphonicacid
coY Aahy cocy Cho
Fech
m- Bromocethenoe
M
CAleobenzekolyd
-Tageter wi
hemical reactns of canb ylic aid :
1.). Fomation aahydide:
Conc
Ethanoic onhydnde
cycoojn; fpidine,
cyco
Acetie onhydide
ycojc1i
ycoowa yco
Acatc cahydnde
2. Gsterifeation;
RCoOR'
3Cycoan
Soy is prefemed becoue the other two poduels
CsO, and HCI) are gae and eSape He ree t on
making the punfiataon praduck easier
-Tagetker wick
4. Reecon th ammonia
Amu.enzoz
Benzamide
[olcon
Phthalic co& Ph thelCmi de
S, Redetion
(iA ethe
Cnçoon
G. Decaboxylation1- Uging Soda- ime Neot Cao)
3:4
t
c
gem. di casayeaud
Malonic cud
Propane-, 3-dioic cid undepo decansaylaton
Siy
heetg
|2
R--cooH
(x-c, B)
CIcycoan.Rude C; cH coOn(Beklooctete
RedP
add
ChecoOH
Thehlasetc cu
Br, RedP
Br,RedP CoOh
BroMopropoceit K-di brma
Pepionie aid - propionie ud
coon
B. Ring Subotit tron t HB r
3Nitbenzie
Nitteaon
t no
3-Shobenzojc cad
gra is electon -ewithduis, thersefe
ie is meta- dite ang Catby'ic aeido, hoere do not