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. Naturally occurring $?$ -amino acids are typically in the L-configuration. The Fischer projection of $L$ -alanine is shown. L-alanine Identify which structures are equivalent to the L-configuration. Identify which structures are equivalent to the L-configuration.

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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. Naturally occurring

?

-amino acids are typically in the L-configuration. The Fischer projection of

L

-alanine is shown. L-alanine Identify which structures are equivalent to the L-configuration. Identify which structures are equivalent to the L-configuration.

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