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Prof. Darius Zlotos Tutorial 4 Organic Chemistry I

This organic chemistry tutorial document contains questions asking students to identify whether given molecules are chiral or achiral, assign absolute configurations, identify stereocenters and their configurations, determine if compounds are enantiomers or diastereomers, convert a line structure to a Fischer projection, and explain why a compound with two stereocenters is not optically active. The document contains molecular structures as examples for students to analyze concepts relating to stereochemistry, chirality, and isomerism.

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0% found this document useful (0 votes)
50 views2 pages

Prof. Darius Zlotos Tutorial 4 Organic Chemistry I

This organic chemistry tutorial document contains questions asking students to identify whether given molecules are chiral or achiral, assign absolute configurations, identify stereocenters and their configurations, determine if compounds are enantiomers or diastereomers, convert a line structure to a Fischer projection, and explain why a compound with two stereocenters is not optically active. The document contains molecular structures as examples for students to analyze concepts relating to stereochemistry, chirality, and isomerism.

Uploaded by

musicslave96
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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Prof.

Darius Zlotos Tutorial 4 Organic Chemistry I


___________________________________________________________________________
1. Are the following molecules chiral or achiral ?

a) b) c) d) e)

f)
CH3

CH3

2. Assign the absolute configuration of the following molecules

a) b) c)

3. Identify all stereocenters (asymmetric carbons) in the following


molecule and assign the absolute configuration for each
sterecenter

4. Are the following compounds enantiomers, diastereomers or neither


nor ?

a)

1
Prof. Darius Zlotos Tutorial 4 Organic Chemistry I
___________________________________________________________________________

b)

c)

5. Convert the following dashed-wedged line structure into a Fischer


projection (place the longest carbon chain in the vertical position in
the Fischer projection)

6. Explain why the following compound is not optically active


despite two stereocenters ? (meso compound)

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