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CHM 3372 - Pre-Lab 4 PDF
CHM 3372 - Pre-Lab 4 PDF
I
st ! ↓
OH crotonic acid ethylcrotonate ethyl lewlinate nexanal cyclohexanecarboxylic acid cyclohexanone cyclohexylamine
2- hexanol levulinic acid
(carb.acid) Ester) Lester glucose (carb.acid)
-
no heat generated heatgenerated +
acetyl chloride
COHPphenols)
ethylcrotonate 2-hexanol
ethylevulinate crotonic acid
hexanal levulinic acid
glucose cyclohexanecarb.acid
cyclohexanone
cyclohexylamine
⑩bubblesobubbles +
yellow magentaburgundy + bicarbonate
(carb. acid)
hydroxamic
Lester) 1 crotonic acid
↑ylcrotonate
n levulinic acid
hexanal
glucose one OH
cyclohexanecarb.acid
cyclohexanone 2-hexanol
cyclohexylamine
brown precipitate t
no precipitate yellow precipitate +
no
precipitate
1 kMnoy(c 0)
tone
=
isdoform
<methyl
* ↑
ethylcrotonate "ethyl lewlinate OH
levolinic acid crotonic acid
insoluble soluble +
cyclohexanecarb. acid
solubility
Lether
(H20H
o
cyclonexylamine
·!,"vi,i cyclohexanone
hexanal insoluble soluble +
glucose
solubility
(water)
1 2,4 1ND
-
Caldehydes ketones) ⑭
0
↑ OH
hexanal OH
↓ !
↓
cyclohexylamine cyclohexanecarboxylic acid levulinic acid
cyclohexanone
insoluble soluble +
solubility
(water)
⑧ NHz
nexanal L
cyclonexylamine
Beilstein +
iquition
Br
H OH 0H
a - 0 Cl
↑H2qH
-
3r
0 0
=
4
Broomaophenomepanoramline
p-bromoanisole
1
2-bromoethylbenzene
isromoseraldehyde-bombozakonolacorobenzoicacid methylchlorobenzoate
of chlorotoluene
p-cupidpanone
(phenol)
no heat
generated heat generated +
acetyl chloride
COH's Aphenols
2-bromoethylbenzne
4-bromobenzyl alcohol
7-bromobenzaldehyde 1-chlorobenzoic acid
methylo chlorobenzoate p-chloropheno
o-chlorotoluene o-chloroaniline
p-bromoacetophenone
p-bromoanisole 9orange/yellow solution blue/green precip. +
p-bromoacetophenone 4 bicarbonate
(carb. acid)
p-bromoanissle methylo-chlorobenzoate OH 0 -
0H
yellow precipitate
Br
p-chloroaniline p-chlorophenol
no precipitate brightorange precipitate +
2,4 1ND
-
o-chlorotoluene
p-bromoanissle
n-bromoblecaldehyde
1 1 gNOs
-
1
o -chlorotoluene p-bromoanisole
2-bromoethylbenzene
faster slowest
! NaI
Cl
chlorotoluene
↓
p-bromoanisole
Beilstein Ignition
O CI
Br
Br d
&X
1-bromobsn tchbrobutane
Br
1-bromo-2-ethoxyethane isdobutanechloro-propanol Br
Ether (10a(c)
a-chloro-a-butanone
(methyl ketone) allylbromide chloroacet,ethyls-bromopropionate - butylbromideand
(30nalide)
-
yellow solution blue/green precip. I
chromic acid
(10,20,308Hs) chloroacetic acid
1-bromo-2-ethoxyethane 3-chloro-2-butanone
1 bromobutane
allyl bromide 3-chloro-propanol
-
chlorobutane
ethyl 3-bromopropionate
1-
1 iodobutane
t-brtubromide CO2 bubbles CO2 bubbles
-
no +
bicarbonate
(carb, acids)
21 Cl
magenta/burgundy
Ot
yellow +
OH
3-chloro-propanol
hydroxamic chloroacetic
Lester) acid
Br
1-
bromo-2-ethoxyethane &X
I-bromobutane
3-chloro-2-butanone
1- chlorobutane allyl bromide
1
-
iodobutane t-butyl bromide
ethyl 3-bromopropionate
no yellow precipitate +
precipitate
iodeform
(methyl ketone)
CI
1-
bromo-2-ethoxyethane
1 -
bromobutane
allyl bromide
1- chlorobutane t-butyl bromide
1
-
iodobutane
3-chloro-2-butanone
brown precipitate t
precipitate
no
KMnoy(c c) =
1
1-
bromo-2-ethoxyethane Br
1 -
bromobutane
1- chlorobutane
1 iodobutane
allyl bromide
-
t-butyl bromide
Br2/CCI
1 -
bromobutane
O
1- chlorobutane
Br iodobutane
1
-
1-
bromo-2-ethoxyethane t-butyl bromide
niht>Bto conte
CI Br
chbrobutane I bromobrtane isdobutane
--buybromide
Beilstein
↑Ignition
Doheranos
benza n carnaini. w.emma acpanini "**anethole
01
-
-
anisole
on
no heat
generated heat generated +
acetyl chloride
COH's Aphenols
3-phenyl-1-propanol
&etophenonenapthalebenzasee
p-aminopheno
methyl
benzaldehyde-7-cawb.acid p-hydroxyacetophenone
cinnamyl alcohol o-tolvic acid
p-tolvidine
1 2,4 1ND
15
-
chromic acid
↑ Caldehydes & Retores)
anethole (10,20,300H's)
anisole acetophenone p-aminophenol 3-phenyl-1-propanol
methylbenzoate
napthalene p-tolual dehyde P-hydroxyacetophenone benzaldehyde-7-cawb.acid
p-toluidine cinnamyl alcohol
1
(methyl ketone) (methyl ketone)
H ↑
↑ p-aminophenol
p-tolvidine HOP-hydroxyacetophenome
no CO2 bubbles CO2 bubbles +
anisole
- 1 KMnoy(c c) =
1
0x/
hapthalene OH
methyl benzoate
3-menyI-propanol cinnamyl alcohol
1 2,4 1ND
-
no
precipitate brown precipitate t
Caldehydes & Retores)
1 KMnoy(c c) =
1 H0
-04 7
anisole
napthalene
o-tolvic acid benzaldehyde-4-carb.acid
-
insoluble table anethole
solubility
CH2SOn)
x.
naphthalene anisole