Skip to main content
Chemistry LibreTexts

SC8. Biological Building Blocks: Carbohydrates

  • Page ID
    4133
  • \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \) \( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)\(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\) \(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\)\(\newcommand{\AA}{\unicode[.8,0]{x212B}}\)

    SC8. Biological Building Blocks: Carbohydrates

    • The naturally-occurring carbohydrates are chiral.
    • Glyceraldehyde is the grandmother of carbohydrates.

    Wire Frame

    Ball & Stick

    Spacefilling

    Wire Frame

    Ball & Stick

    Spacefilling

    • The "last" chiral center in other carbohydrates all have the same configuration as the chiral center in glyceraldehyde.

    • Fischer projections are drawings that are sometimes used to show stereochemistry in a different way.
    • The groups to left and right of the Fischer projection are coming towards you.
    • The groups on top and bottom are going away from you.
    • The carbon chain is drawn vertically with attachments at the sides.
    • Normally, the chain is oriented so that the "highest priority functional group" on the chain is at or near the top of the chain; that usually means the group with the most bonds to oxygen. In glyceraldehyde, the CH=O group is drawn at the top rather than at the bottom.

    Problem SC8.1.

    What is the absolute configuration of L-glyceraldehyde? What about D-glyceraldehyde?

    Problem SC8.2.

    Draw the following molecules as Fischer projections.

    Problem SC8.3.

    Convert the following Fischer projections into wedge-dash drawings.


    This page titled SC8. Biological Building Blocks: Carbohydrates is shared under a CC BY-NC 3.0 license and was authored, remixed, and/or curated by Chris Schaller.

    • Was this article helpful?