Isomers and Stereochemistry - staff.uny.ac.idstaff.uny.ac.id/sites/default/files/pendidikan/Dr. Sri...
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Chapter 6
Isomers and Stereochemistry
Essential Organic ChemistryPaula Yurkanis Bruice
Disampaikan oleh : Dr. Sri Handayani
2013
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Review of Isomerism
Isomers – Compounds that have the same
molecular formula but do not have identical
structures.
Constitutional Isomers – differ in the way
their atoms are connected.
Stereoisomers – differ in the way their
atoms are arrange in space.
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Constitutional Isomers
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6.1 Cis-trans isomers
Differ in the arrangement of their atoms in
space (cannot interconvert)- Alkenes.
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Cyclic structure.
6.1 Cis-trans isomers
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6.2 Chirality
Chiral –Nonsuperimposable on its mirror image.
Achiral – Superimposable on its mirror image.
If a molecule (or object) has a mirror plane or an inversion center, it cannot be chiral.
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Chiral or Achiral?
Brandy snifter
achiral achiral
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Chiral or Achiral?
Shears
chiral
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Chiral or Achiral?
Beer mug
achiral
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Chiral or Achiral?
Hiking boot
chiral
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Chiral or Achiral?
Baseball glove
chiral
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Chiral or Achiral?
Boat propeller
chiral
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Chiral or Achiral?
Desk chair
achiral
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Chiral or Achiral?
School desk
chiral
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Chiral or Achiral?
cis-1,3-dimethylcyclopentane
mirror plane
achiral
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Chiral or Achiral?
trans-1,3-dimethylcyclopentane
chiral
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Chiral or Achiral?
1,1-dimethylcyclohexane
achiral
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6.3 Asymmetric centers
An asymmetric center is an atom that
is bonded to four different groups.
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Chiral or Achiral?
2-butanol
mirror imagechiral
Asymmetric
center
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Chiral or Achiral?
2-bromopropane
achiral
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6.4 Isomers with one asymmetric center
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6.4 Isomers with one asymmetric center
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Enantiomers
A chiral compound and its mirror image are
called enantiomers.
2-butanol:
enantiomers
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Enantiomers
Asparagine:
enantiomers
mirror
plane
C
COHO
CH2
H NH2
CO NH2
C
CO OH
CH2
HH2N
COH2N
D-asparagine
(from vetch)
sweet taste
L-asparagine
(from asparagus)
bitter taste
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6.5 How to draw enantiomers
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6.6 Naming enantiomers: the R,S system
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Absolute Configuration
R and S
• Assign priorities to the remaining groups based
on atomic numbers.
• Clockwise (highest to lowest priority) R
• Counterclockwise S
=H C
CH3
OHCH2CH3
C
CH3
HO CH2CH3
1 2
3
(R)-2-butanol
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Absolute Configuration
Assign priority:
• Atomic number of atom directly bonded.
• If the same atom is bonded, go to the next atom,
etc.
• Groups containing multiple bonds are treated as
though multiple atoms were attached:
C O = C
O
O
C
C N C
N
N
N
C
C
=
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Absolute Configuration
Determine the absolute configuration of the
following compounds:
C
H3C
BrCl
H
C
F
DCH3
H
C
(CH3)2CHCH2
CH3CH2CH2CH2Cl
H
C
C
CH3CH2C
H
O
H
N
1
23
4
12
34
1
2
3
41
23
4
SR
S R
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Absolute Configuration
Determine the absolute configuration of the
following compounds:
CCH3
H
CH3CH2 CH
CHCH3O
OH
CH3
CCH3
H
CH3CH2 CH
CHCH3O
OCH3
CH3
C
CH2=CH
CH3CH2CH3
H
C
CH2=CH
(CH3)2CHC
H
CH
1
2
3
4
SS
1
2
3
4
1
2
3
4
1
2
3
4
S R
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Plane-polarized light is produced by passing
normal light through a polarizer.
6.7 Chiral compounds are optically active
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Optical Activity
When plane-polarized light passes through a
solution of achiral molecules, the light emerges
from the solution with its plane of polarization
unchanged.
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Optical Activity
However, when plane-polarized light passes
through a solution of a chiral compound, the light
emerges with its plane of polarization changed.
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Optical Activity
Optical Activity – The ability of a compound to
rotate the plane of polarized light.
A compound that rotates the plane of polarization
is said to be optically active.
Chiral compounds are optically active and
achiral compounds are optically inactive.
A polarimeter is used to make such measurements: