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Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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
Transcribed Image Text:3) What is the relationship between the molecules shown? (Same molecule, enantiomers,
diastereomers, constitutional isomers, conformations, cis-trans)
CI
CI
CI
H
Hum
f
X L
H
Hmmm
CH₂F
F
CH3
H
H
H
B)
H3 C
H
H
CH3
F
H.
H3 Cl
Br
Br
XX
Br
X X
CH3
F
Br
H
C)
F
D) F

Transcribed Image Text:Н
ОН
Н
хххх
E)
Н
Н
F) H
Ommy
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- Which of the two molecules below has more stereoisomers? O O I O Br B. I, because II is a meso compound C. because it has more chiral centers O D. II, because I has no enantiomer A. They have the same number of stereoisomers Br E. II, because I is a meso compound II Br Sarrow_forwardCan u explain ur answerarrow_forwardCompound 1 Br Bri НІ T ... H The correct IUPAC names are: Compound 2 H Br Br I.. H Br The compounds are diastereomers not isomeric enantiomers identical constitutional isomers Compound 1: (2R, 3R)-1,2,3-tribromobutane, Compound 2: (2S, 3R)-1,2,3-tribromobutane Compound 1: (2R, 3S)-1,2,3-tribromobutane, O Compound 1: (2R,3R)-1,2,3-tribromobutane, Compound 2: (2S,3S)-1,2,3-tribromobutane Compound 2: (2R, 3R)-1,2,3-tribromobutane O Compound 1: (2S,3S)-1,2,3-tribromobutane, Compound 2: (2R,3S)-1,2,3-tribromobutanearrow_forward
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