Alcohol Phenol & Ether

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y HeHO ( HcH,o -

LAH
isfey oracid redvee not o SBH Point)
;- (oP.
(esko)
n,) (Nn
LIAIHy t
Boro
( LiAH,
CHto CH
-CH-cH But
cHO =CH- PhcH
(Ketoxc) (Al4.
NaBHy
Tedote LiAH, >R-CHa-oH
cHs ( ey
po
bond double LiAHy
me fxn. Reducion &
BHy Na
(Atrarkors
fov) HoH (H,o Ac), (Halo OHOM
HoH
CH, f-cH
HBO
ikov) Htoy Adliion H/THE 6, HBO
hnt
Catbocafon
oH
CHaR-cH-
pos) Gearany
} (
CH-CHa R- cH =cH B-
a)
Hojor
akie)
Alcohol Hop
ther
11ker f
Pheno Alcohal
From Grignavd Reogat
xor
-oty
2+

Mg(o)

0 Ajdic Notuye
* fan alays procaedin the prnd
RoH H weoto aid

Na] Ro Na
Nat
ROH RoNa

NaH co, No Rn-(Coz H, co, is Neyl ofeohof


ait compare

R-c-oR
ROH

R-c-oe'
( L-R onhy encIz )
Luca's Test
1 poH No turbidity (soi)
turiity in mgte
turbi ity in dee.
3>2
ith K, , PKs,sox, Red PX,
(Mo vearangernet)

Red

& oxdtion of
o< tohals (Hild o.)
H

(akon) R-c-H (Aldyde)

(2' RoH)
(Ktone)

(3° RoH) No

) Mild ozidising Agat chlanchorete)


Jichromote 2

coltin's reget.(cro, + 2

Jone' s veaqert (( cro,+ acctone) cHs~een,


8 2 pnpanone )
Ce /s0o°c (eait ith 3° pOH)
Pyridne
dukydrein (ofkena )

AlyleR-cH=CH cH, -0H)


(8peiof Cose Y
Ph-cO
)

(onlyHn2atyhe cHO
Arega ) alcoh )
uylie
CHo

8fong oridiing tel.


R-C- H
(
(1'

No odofYn.
poH hue, to chohe mi ho
song o.A * (Notei
)
k, Cr, 0, /*
Conc. NO3
CyO,t H,soy (Ions's Reage)
Halojovm (x= ct, I)
| venby oY cHa-cH- (gmp)

He n tnce
aleohof
do nat regvre
Atie aeid Phenl > yclo hexaof.
phot.

A.A
ODow's Prcey
NaoH

B062 K
From Benzene
oleum
H soy H

@ Aniline Nc
NaNo,
Hea
CBen2ene
Dieniom claide)

CH
CHs
(Come

Properies o Phenof.
Ajdic Nofure.

Na0H
hoH Nal
Phonat H,o

No Rnn
(H;eo3 stanger
aid than pÅ oH )
NO
o, N. N.O

NO,
(Picrie AGd)
OH

Na Hco, . NO

NO2 NO,

ONq
Na Hco

(paa) No,
(fara ore ajdic
Hhan ortho hare
Naco, No Roen,
(ordho)
ssteriti cotion (sem ptcohol)

R-C -H ph-0c-R + Ho
phot
R-c-c|

Pho- c -R + RCOOH
+ Hea

-oH
cHCI3
-7emann
R Reimer
Acid
oH Na
CO (æ) oNe oHt
Ran. Kolbe's
carbon
tn aorm,
phuy oibrans (weter)(Bromrine
()
Bo
ortho) (
(paa)
B2
H (8x*)
Brominotion @
ortho Para
<
-valatlity
solsbk
in not i-e,
OH
oho >Pare
Note Point eoiling
NO (Mojo) stength Acilic .
-No pormn) ( (ortho)
oH
HNOy
Picte
/HSoy HNo, Conc.OH ntroion) mono ( 3
Aubshtoton, Aromaic sledvophilic
Zn
ph -H

odotion
Na, C,07
P-Benz0qujnone)

aNote : sletropile invaled in Reimer -Tieman


TËean Y
pjchloocavbene

Ethey
(R-oH ko double kike H,o kof do ;e- 0-p)
9 9ehydyofon of cohet. (R-oH
acohot.
HSOy CHa- CH,-0- CH, - CH,
| ind pro)
(proces)
CHa-c, OH,

wliamson's sher ythesis (Tmp )

SN2
A-o-R (fav. cond; R-x -- 1°)

SN?
(3)
CH,oNat
cHac-c
(isobitene)
froperhy

oY Yesoncn co
H

la , 2'
thn SN
otherise SN2J
cHa-0-cH,-CHe

H CH,-I+ c,c,-oH
H

Hx

(Resonouce)

ph cHa

E.As (Paa Mojor


rominotin Anisle

(Aisale) fe
B (tor)
e Ntotlon (No, )
Conc. HNo,
Cone. H,s0 No (Major)
(Rnong i pooibie )

ogl-tion
-coe

HX

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