Stereochemistry in biological molecules is often denoted by the D- and L- convention, instead of the R- and S- configurations determined by the Cahn-Ingold-Prelog methodology. Historically, the glyceraldehyde enantiomer that rotated plane polarized light clockwise was arbitrarily designated as D and the other enantiomer was designated as the L configuration. The D-glyceraldehyde Fischer projection is shown. D-glyceraldehyde H H- -OH CH₂OH Identify which structures are equivalent to the D-configuration. H CH₂OH 76. OH CH₂OH H- -OH ☐ O H ОН -CH₂OH K H H Incorrect HOCH2 H OH t H OH CH₂OH K.

Stereochemistry in biological molecules is often denoted by the D- and L- convention, instead of the R- and S- configurations determined by the Cahn-Ingold-Prelog methodology. Historically, the glyceraldehyde enantiomer that rotated plane polarized light clockwise was arbitrarily designated as D and the other enantiomer was designated as the L configuration. The D-glyceraldehyde Fischer projection is shown. D-glyceraldehyde H H- -OH CH₂OH Identify which structures are equivalent to the D-configuration. H CH₂OH 76. OH CH₂OH H- -OH ☐ O H ОН -CH₂OH K H H Incorrect HOCH2 H OH t H OH CH₂OH K.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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