Consider the following Fischer Projections: CH2CH,-CıC-NH2ČH,CH3CH,CH,H2N-CH2CH,CH,CH,-CIH,N-CICH,OHH2N-H2N--cı-NH2H,N--CıCI--NH2CH,CH3ČH,OHMANMENMONMUN11. a meso compound12. enantiomer of compound MUN13. optically inactive compound14. diastereomer of compound MON

Here we are classify the following pair as enantiomer diastereomer from the given compound…

CH2CH, -Cı C-NH2 ČH,CH3 CH,CH, H2N- CH2CH, CH2CH- -CI H,N-CI CH,OH H2N- H2N- -cı -NH2 H,N- -Cı CI- -NH,. CH,CH3 ČH,OH MAN MEN MON MUN 11. a meso compound 12. enantiomer of compound MUN 13. optically inactive compound 14. diastereomer of compound MON

CH2CH, -Cı C-NH2 ČH,CH3 CH,CH, H2N- CH2CH, CH2CH- -CI H,N-CI CH,OH H2N- H2N- -cı -NH2 H,N- -Cı CI- -NH,. CH,CH3 ČH,OH MAN MEN MON MUN 11. a meso compound 12. enantiomer of compound MUN 13. optically inactive compound 14. diastereomer of compound MON

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter4: Organic Compounds: Cycloalkanes And Their Stereochemistry

Section4.3: Stability Of Cycloalkanes: Ring Strain

Problem 8P: Each Hâ†”H eclipsing interaction in ethane costs about 4.0 kJ/mol. How many such interactions are...

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Question

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Consider the following Fischer Projections:

CH2CH,
-Cı
C-NH2
ČH,CH3
CH,CH,
H2N-
CH2CH,
CH,CH,
-CI
H,N-CI
CH,OH
H2N-
H2N-
-cı
-NH2
H,N-
-Cı
CI-
-NH2
CH,CH3
ČH,OH
MAN
MEN
MON
MUN
11. a meso compound
12. enantiomer of compound MUN
13. optically inactive compound
14. diastereomer of compound MON

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