Assigning R/S on Fischer Projections

The video tutorial explains Fischer projections, a method used in stereochemistry to represent molecules, particularly in organic chemistry. It covers the basics of Fischer projections, how they differ from other notations, and their application in visualizing molecular geometry. The tutorial also details the process of assigning R and S configurations to molecules using the Cahn-Ingold-Prelog convention, emphasizing the importance of understanding the orientation of bonds in Fischer projections.

Discuss the implications of using Fischer projections for linear carbohydrates.

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What challenges might arise when interpreting Fischer projections?

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Describe the process of determining the stereochemistry when the lowest priority group is on a horizontal bond.

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