ISOMERISM AND STERIOCHEMISTRY
“Different compound having same molecular
formula are called isomers and phenomenon are called isomerism”.
Greek=isos—to same or equal,
merisis—part or constituents.
Isomerism is classified in to two
parts-----
1=structural isomerism
2=stereo isomerism
structural isomerism—Same molecular
formula but different structural formula.
structural isomerism are 7 types—
1=chain ,nuclear & skeleton
isomerism—same molecular formula but different carbon chain.
Ex-- n-pentane
, iso pentane & neo pentane,
Butanol-1
2-methyl propenol-1, Butene-1
& 2-methyl propene , Pentynene-1
& 3-methyl butyne-1, Pentanol-1
& 3-methyl butanol-1, Ethyl
benzene & xylene [o ,m ,& p] .
2=position isomerism— Same molecular
formula but different in position of functional group.
Ex-- butene-1
& butene-2.
Butyne-1
& butyne-2.
1-chloropropane
& 2-chloropropane.
1,1-di
chloroethane & 1,2-di chloroethane.
Propanol-1
& propanol-2.
O-xylene
, p-xylene & m-xylene.
Pentanone-2
& pentanope-3.
3=functional group isomerism— same
molecular formula but different functional group. Ex--
4=Metamerism—Same molecular formula
,same functional group but different in alkyl group joint by functional group.
Amine—Methyl propyl amine & di ethyl amine & Methyl iso propyl
amine ,
Ether—Methyl propyl ether & di ethyl ether & Methyl isopropyl
ether ,
N-group—di methyl propyl amine, di
methyl iso propyl amine , Methyl di ethyl amine,
Ketone— di methyl ketone , Methyl
propyl ketone , Methyl isopropyl ketone,
5=Cyclic or ring isomerism= Same
molecular formula but different in chain open & close ring.
Ex=Butene-1 & cyclo butene &
methyl cyclo propane.
NOTE=Ring chain isomerism are always
functional isomerism.
6=Isotopic isomerism= Same molecular
formula but different in isotopes of element.
Ex=Methane-=C-12
& C-14,
Water—H-1 & H-2,
Formaldehyde —O-16 & O-18.
7= Tauomerism or
Dynamic equilibrium=Same molecular formula but different dynamic nature of
hydrogen ion or ring substituents. It also called “DESMOTROPISM”.
Desmo = Bond & Tropos = Convertation.
Tautomerism can be
classified as-
1-Open system
tautomerism—
2-Ring chain
tautomerism—
3-Valance tautomerism—
NOTE—Acito acitic ester is the
best example of tautomerism. & Benzophenone (C6H5—CO—C6H5)
does not show tautomerism because not dynamic hydrogen .
stereo isomerism=Same constitution but different
spatial arrangememt.
Sterioisomers are 2 types---1-Cofigurational isomerism—
2-Conformational
isomerism—
1-Configurational isomerism= The different spatial arrangement of atoms in a molecule which are not
interconvertable without breacking of bonds & formation of bonds are
called configurational isomerism.
2-Conformational isomerism=The different spatial arrengement of
atoms in a molecules which are radily interconvertable by rotation single bonds
are called conformational isomerism.
1-CONFIGURATIONAL ISOMEREISM=Configurational isomers
are 2 types—
A> Enantiomers—Non superimposible mirror image
B>
Diastereoisomers— Not mirror image.
“CONFIGURATIONAL ISOMERISM “Are 2 types—
1—Optical isomerism-
2—Geometrical isomerism-
1-Optical isomerism-Same molecular formula, Same
structural formula but different in configuration of valance ligands are called
optical isomers & the phenomenon is called optical isomerism.
A>
Plane polarized light--If Ordinary light
is passed through a nicol prism ( 2-prisms of Iceland spar,CaCo3 )
,then light vibrates only one plane is called plane polarized light & that
plane is known as “plane of polarization” The whole process is called
“polarization”.
B> Optical
activity-- BIOT(1815) passed organic solution of substances( like Glucose,
Fructose, Sucrose ,Lactic acid etc.) in plane polarized light. He found a
certain property to rotate with angle
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