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ATION OF ORGANIC COMPOUNos
âOrganic Compounds
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Distilation: This wectwnque is
stances whe ah
present in an aqueous
ât's separated by shaking it with atvorganie
Unwhich tis more sou
hananaine neous schon snout |
yh each other
thaninwator
Misinct layer which can be separated by
/unnet
âobiained
tis an important technique extensively
mixtures ino thei eamyponents
Principle Involved tis classed ito two main
ew
an
âMeaeN yy! + AP
FOASCA > 1Fo
[(©Testot Halogen
X 1A Aa
tonne
© A yellowish procpitato soluble, sparingly sokitio in|) % ot halogen
8CN + Fo" fron
â© Avfuteprecate solibie in NH,OH shows prosence of |
Organic Chomistry
SITE eopannl
Basic Principle
FeGHFAEN aH
(FaKCN,NOS* containing togen inn
sd bt pes saan | (0) Hane
1 ata ath
| Mass ofAaX orm
ees Ieee aa âOrganic compound
'NH{OH shows prosenco of
2 Ayellow precipate insoluble inNH,OH shows prasenco| |) Sulphur
olloaine
|| (0) TestorPhosphorus,
"re adsorbed on an)
nt derees. Common used
Imponenis of a mixture
Papor|
yr. halogins and phos
âare dolociod by
phosphorus
âLassaigne's lost. Tho.
converted tom
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Caius mothod:
organic
Letmass ot compound =mg
âew, | Masso1@as0,=m,9
() Dumas method
Ltvolume of ogon a T= Vt Ty
Nass ofan conpotid = 0
(W Kjoldants Method
(NH)
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(7) QUANTITATIVE ANALYSIS
(A) Nitrogen fs estimated by Dumas and Klldahi' method I
Pea
PĂ©reontage ot nitrogen
Organic compound + 1,50, » (NH),S0,
dommeatte
\4 i ares we
1
Ve :
yw ap fompoun
YF, otis of eampound =
gaxvero) 1â)
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Molar inassgot N40,
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Road: rit 110005, Phoneâ O41-4763345
nd Technic
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1a] No oF RHURIPOW2MOY IMD