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6.1
6.3
6.4
6.5
6.6
6.7
6.8
6.9
6.10
6.2
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mirror images
sp3-
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6.1
6.1 CH3X , CH2XY CHXYZ
CH3X
CH2XY
CHXYZ
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enantiomers
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6.2 (a) H OH
CO2H CH3 (b) CO2H
CH3 H OH
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6.2
chiral
chirality centersstereocenters
5-
5-bromodecane C5
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p.181
nonchiral
achiral
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p.182
6.3 (a)
(b)
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6.2
6.1
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6.2
3-
OH
H,
OH, CH3 CH2CH3
3- CH2
CH3
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p.183
6.3
6.3
2-
C2
C2 CH3 H
C=O CH2 2-
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optically active
polarimeter
6.5
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6.5
levorotatory
dextrortatory
(2)
(1)
(2)- (1)-
6
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p.185
[a]D
6
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6.4
6.4
1.20 g cocaine[a ]D16 7.50
mL 5.00cm
Biot 1848
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Louis Pasteur
28C
6.6
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6.6
6.5
configuration
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p.187
6.7
123
R R configuration
rectus 123
S S
configuration sinister
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6.7
4
123
R 123
S
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p.187
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6.5 R S
R S
180
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6.5 ()
6.6
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6.6
(1) Cl(2) CH2CH3(3) CH3(4)
H H
123
90
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(b)
3
1 2
R
(R)-2-
6.5 ()
(a)
2 3 1
R
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n 2n
2--3-C2 C3
22 4 6.10
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6.10
2--3-
diastereomers
6.2
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p.191
6.7
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2R,3R 2S,3S
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2R,3S 2S,3R
2R,3S 2S,3R
180
C2C3
6.11
6.11
mesocompounds
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6.11 C2C3
6.3
(1)(2)
(1)(2)
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6.7
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6.7 ()
-1,2-
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-1,2-
C1 C2 C1
C2
-1,2-
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6.8
RCO2H
2R,3R 2S,3S
--
RNH2
5050
racemic mixtureracemate
d,l
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6.12
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6.13 (R)-1-
6.8
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6.8
10.6 RCO2HR
OH
RCO2R
()- CH3OH
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6.9
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6.14
constitutional isomers2.2
stereoisomers2.8
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p.198
6.14
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6.10
1,8-limonene()
()
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p.199
fluoxetine
Prozac
fluoxetine
S
6.15
p.199
p.200
10
6.15
(a)
p.200
6.15 (b)
p.200
6.16
NAD
CH3CHO
CH2
6.16a
6.16b
OHCH3
Hb
Ha
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p.201
V
Penicillium
2S,5R,6R
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p.201
11
()
()
Ibuprofen
AdvilNuprin Motrin 5050 R S
S
R
S
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p.202
12