Name Rxn

Organic
$ Conversion

BRANCH ALLO
a) ALDOL CONDENSATION :

CHS -

Cfo
+ H CH
-

,
CHO EI Ctg -

no .¥ocH5cH -
- en cao
-

b) CROSS ALDOL CONDENSATION :

cuz
- % - H t H -
E-
H Ho -

cuz Ctf
- -
% - H .

) BALZ SCHIE MANN REACTION :

-

IN H2 "
I Nat BE
fog +

fluoro benzene
Aniline

d) BENZOIN CONDENSATION :

In die,
"

⇐ Even -Ee takin

'
ex - -

Benzoin .

BRANCH ALLO
C) CANNIZZARO REACTION
CF Ona
:

LCH IH )
-
c' + NaOH → CHGOH t H - -

I CHO + NaOH → -

CHIH tf -

COO Na
Sod Benzoate
Benzyl alcohol .
.

f) CARBYLAMINE REACTION :

CHzCHgNHg + CH Clg +3 KOH CH

Ctf NEC -13 KCI -13110
- -

NH + CHAZ -13 KOH calc )

Is - NIC -13 KCI -13110
, .

g) CLEMMENSEN REDUCTION :

Cuzco cuz + 4GB Etat ! CH, CHACH, t H2O

'
CHS CHS +
f.jo + acid EICH , Hao

BRANCH ALLO
 h) DECARBOXYLATION REACTION :

- 004+2 NaOH ¥fk + Ng cost H2O

i) COUPLING REACTION :

Nz tf
-
-
out HC l
-

NaCl + E- on
K hydroxy azobenzene
-

-
NaCl t -
NH
, E- Naff -
NH
,

p Amino azobenzene
-

j) DIAZOTIZATION REACTION : Nitrous Acid

←

NANO → HOMO + HCl

,
+ HCl

¥442140
'

+ HOMO + HCl

E- TARD REACTION CHO

cite :%% ÷÷:u

k) :
:c
⇐¥
"
.

Brown complex Benzaldehyde

Toluene
BRANCH ALLO
d) FINKELSTEIN REATION :

GHS -
Br + NAI efA Gtf -
I + Na Br

my f- 17719 REACTION : pm
citing ⇐ Lost
-
> tania "

h ) FRIEDA L CRAFT REACTION :

i) Alkylation ii) Acylation

" coctlz

tatsu ¥7 ,
Inc ,
tudou.fi#EItHciAeephenone
O ) GATT ER MANN REACTION :

Thu c>
AE, PINA
1- N
+
2

BRANCH ALLO
 b) GABRIEL PH THAL IMIDE SYNTHESIS :

'

NH + KOH Nk
-
t
GHS III
'
-

Phthalimide pot .
phthalimide

IN GHS taiyo EI%: 1- Ca Hs MHz -

Phthalic Acid
N phltralimide
-
Ethyl

g) GAITER MANN KOCH REACTION :

to + HU ¥¥x ¥50 + Hcc .

Benzaldehyde
)
r H V. I REACTION C Hell Vol hard
.
Zelinsky Reaction)
Cte, OH tusked UCH OH tu GCU COOH
, ,

Ck Red P
Cf C -
COOH e
,

s) HOFMANN AMMO NO LYSIS :

" amine 2.amine 3- amine .

H, Ntr X R NH TR X ¥ R NH R TR X R pl R
#
- - -
-
- -
- -

,
R
t) HOFMANN BROM AMIDE DEGRADATION :
R CON Hg Es
R NH -12 Na Br + , cos -12110 Na
+
Big +4 NaOH
- -

E- CONH, +
By -14 KOH Es Et NH, -12K Bztkzcoz -12140
u) HUNS DI ECKER REACTION :
cc 14
R COO Agt
-

Bra ¥+7 R Br + cost

-

Ag Br .

V) KOLBE 'S REACTION :

"

EI II.97 >
Na
+ co
, n'Ito >
icgiic Acid )

w) REIMER -
TIEMANN REACTION :

III + cub [ EINE na

.
÷÷Y ,
EIFcucoHL.FI]
eFcuo ' '"
c salicylate hyde)

BRANCH ALLO
 X) ROSEN MUND REDUCTION :
a

R - di -
Cl TH, Pd, Bash 's
>
R - d' -
H + HCl

Boiling xylene
SAND MEYER REACTION :
y)
del
El + tea
Caa
→
leg fr
lol
t
+ Hbr ¥ A
Lot
CN
+ Ken

E) STEPHEN REDUCTION :
snag -12116 → snag -12cm
R CIN -12cm ) 1- HCl
-
# R CH -
-
-
NH.HU
ether

4
Boiling H2O
RCHO tNH4U
i) WILLIAMSON SYNTHESIS ,

R X -
+ R' ONA Y ROR
'
+ Max

( Hs I -
t ↳ Hs ONA
-
TCH, O -
-

GHS that
ether .

BPANKHALLO
ii ) WOLFF KISH NER REDUCTION :

KN NHL
-
KOH R.CH, N,
R CHO
-
,
y +
glycol
CH
City COCH, "
y CHS -

Ctf -

,
"
t
- COCH
,
-
CH
,
CHS
iii ) WURTZ REACTION :

r÷IIEnIIIII÷r :# Rrr + Imax

( Hsi:B.ir I.IM IB
-

CH,
. .
.

Denker > Cates t2NaBr

iv) WURTZ -
FIT TIG REACTION :

CHS Et tanar
III.I :B 1¥
-

>
cus
Toluene .