Alcohol, pherol, her

aeachion
Reimes- Tieman
Kxplain in he prescra
taeaked wth chlosofo
when
phenol on
uoe ge
Na0H Rolloued by aciduicahi
salicqlaldehyde ONa
CHO
CHO
GrHclg+Qq Naol

ealaulaldede

Williamson 2tber Synthes

( Explaim alkoxi da
alkoxi de
Sodiumn
Sodium
wben Teact wtb
Alkyl balide
Eooonm ethes R-oR + Nax

R-X+R-ONa

dishinquish
distinguish
ard
2 and e
used to
GTive the est
a n b y d o u s Z n C l 2

alcohol and
Com Hcl
ucas esF ucas Tecaen

precip1kae
gent:-sudden

3 alcohol + kucas ales 5mi

precip1tatt
+ kucas
aeagent . precepiLata
tate
alcool
No precëpi
No
qeagent
dueorhol t tas

Gtive sBoucuze Cumere

Cumene
Prepaea phenol oorp OH
CH
CH -O-0-H
CH3
CHsCH Op H2O

Cumene
bydaopoortde

umene
 using qriqnaad ecant
prcpare

altohol5 H oH Ha0

R-CH-OMgx
H-CHO + RMg X 7
Foomaldebyde Ginqnardnt
R-CHa-OH Jpco
alwho

alcohol
HoH
RHOtt
BCHOoMg x
R-CHD RMqx alohs
oomalodehyde (HCHo
All other aldebydes except
alcónol.
wth RMgX
qive
ushun aeat
alccbol oo
alccbol
phenol
phenol
moTe aidic
move Stabllised.
is Yesornane

iom is
W b i c h

phenoaide
phenot
soluble im ocitu
u oat 1
are
cobols bomdima
A lAl byda ogeo
i i i m o l e ula
Due to alohol
alcohól tBphenol
phensl
test to dishnquish
WTile a Na
Na,
(( ley vescone
wi
phenol qive
dlCohol doesmot etbeunat.
methonolP
mehod
to pepane
Gtive cu
is oomed 9
AspiainMedicime) acid w t acdhc
a cdC
How acid c o t
Saliculic
Haeatment o
By mediup.

ip acid
anhydaide cCoo
Coo H
ocOCH
FooH

o
oH
+CHa fo
Salicuc
Aspiri
acd
Copplete the ecachiom s
ind arsusers by osel
HsOA CH=CHa (Debydadtisn)
O CaH5OH
443K
ooH
Nach co
Ht
CS03 CHa-CHO
OH C2Hs OH
Ethanol etbanal
,4-ainitrop hen

Con HNOg O NOz icic ada)

OH
OH
Benzene
Zn dusE

OH
Y
B cOole
B
oH 4 , 6 -1baomophed

OH
Precipital)
H
oH QH
dil HN03

CH2 Mg BT
A
HCHO d o yetbes

H20
C H c H - O H

dagethca

B+CHgMaY HaD cr
b e n z o q u i n o n e -

HsOu

h a t is rectified spisit 7