TITLE DATE

DIHALO ALK ANE DIOL

ELECTROPHILIC ADDITION NaOH Caa
X
X R R HO-R-R- OH
ALIPHATIC REACTIONS
- -
-

& STRAIGHT-CHAIN COMPOUNDS "

:
cai
LETOPIC coup
infor

AODION explor
AMINE

R -

N * Nuc .

ADDITION H2O
I

cald
⑧ BGOBE CBBEB
6080 OB6888 echopha
*
+

VARIOUS ELIMINATION 450 % Al2Oz cat

ALIENE
.

at
E ALKANE
R D
R =
R
-

·
ELECTROPHILIC ADDITION He 1500 SatM Ni cat .

↳ * S#
[S
3/4/140
Eg
:
Noc ,
xt
Vero
Be

70 /14/670 /40 130SUBSTNDOu ,

04
(a(c)
Appito
Naotic
ZiLut
)
Chophilic
*
AMIDE
- R
So 100
0 = R -
N ,

- Nanon
- C
SUBSTITUTION ·
.

KCNCald
B REFLUX

·
&
HALOGENOALIANES
KEY :
R -
X

R-CENXuwe
·
ELECTROPHILIC ADDITION
HEAT
- (

won
Na
CONC . ·
NUCLEOPHILIC ADDITION
*
SomSATURON
·
·
ELIMINATION
NITRILE
"so
·
NUCLEOPHILIC SUBSTITUTION
,
ACID-BASE NEUTRALIZATION
SODIUM ALKANOATE -

ET
NO ORNAOHsiP
D ·
REDUCTION
=O *
R c
Melt a
-

'

··
A ·
OXIDATION
↳ Nat -

ALCOHOLS

-
Nap O
ACID-BASE NEUTRALIZATION
REFLUX R -
OH

-BASAARO
KMnO4
ESTERIFICATION
·

OXIDATION
·

w HYDROLYSIS

ALDEHYDE REDUCTION LIACH4 DRY

ETHER PRIMARY
*

R-CI
CARBOXYLIC ACID
REDUCTION LiACH4 DRY
ETHER
XDATON MOREFLUX
R -
OH
&
o =
co ⑭
OXIDATION KMOY REFLUX
& 00B888
GREEN
TOLLEN'S SILVER MIRROR K2Cr2Oq ORANGE -

- DNPH ORANGE

1595
.
2 4
&
-

FEHLING'S
KETONE
RED
SECONDARY

F·
OXIDATION KMOY REFLUX

c
,

73 0 1 0 2 6 5 70
R-
C-OH E o =
REDUCTION LiAtHy DRY ETHER

R
140604 2
2, 4 -
DNPH ORANGE
%
& 00B888 10 DOFORM YELLOW
i
,

# 54 k2 Cr2Oq ORANGE - GREEN

(produces sodium alkanoate
10 DOFORM YELLOW

350
Mccat
ESTERO
, TERMARY

*
RI of

· -5
-
R-OH mecha $
250
NO 7 ,
INOT
DOES REDUCE
Appar

SUBSRNRONI
"

350455 T
pop
o
HYDROXY NITRILE
Sis
#
!#
#

C
R-
ACYL CHLORIDE
0
=
R - c
ve

!!

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