D and L Configuration of Sugars Quiz
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Questions and Answers

What determines whether a sugar is in the D or L form?

  • Optical rotation
  • Position of the carbonyl group
  • Position of the -OH group on the last chiral carbon (correct)
  • Number of carbon atoms
  • Which form of sugar has the -OH group on the right side?

  • R form
  • D form (correct)
  • M form
  • L form
  • Which sugar is also known as dextrose?

  • Glucose (correct)
  • Galactose
  • Maltose
  • Fructose
  • Match the following terms with their corresponding descriptions:

    <p>D-sugar = Rotates plane polarized light to the right L-sugar = Has the -OH group on the left side Glyceraldehyde = Determines the D or L configuration of sugars Glucose = Rotates plane polarized light to the right and is also known as dextrose</p> Signup and view all the answers

    Match the following configurations with their corresponding characteristics:

    <p>D form = -OH group is on the right side L form = -OH group is on the left side Glyceraldehyde = Used to determine the D or L form of sugars Glucose = Rotates plane polarized light to the right and can be in D or L form</p> Signup and view all the answers

    Match the following terms with their meanings:

    <p>Dextrose = Another name for glucose Chiral carbon = The last carbon in a sugar molecule with four different groups attached to it Plane polarised light = Light that oscillates in a single plane Glyceraldehyde = Used as a reference to determine the D or L configuration of sugars</p> Signup and view all the answers

    Study Notes

    Stereoisomers of Sugars

    • The 'handedness' of a sugar molecule, whether it is a D-sugar or an L-sugar, is determined by the spatial arrangement of atoms around an asymmetric carbon atom.
    • A sugar is classified as D if the -OH group on the asymmetric carbon atom farthest from the aldehyde or ketone group is on the right side, and L if it is on the left side.

    Identity of Sugars

    • D-Glucose, also known as dextrose, is a common sugar found naturally in many foods.
    • D-sugars are more common in nature than L-sugars.

    Configuration and Characteristics

    • The Fischer projection is a way to represent the three-dimensional structure of a sugar molecule in two dimensions.
    • Sugars can exist as anomers, which are isomers that differ in the configuration of the hydroxyl group on the anomeric carbon atom.

    Key Terms and Definitions

    • Anomer: a type of isomer that differs in the configuration of the hydroxyl group on the anomeric carbon atom.
    • Asymmetric carbon atom: a carbon atom that has four different groups attached to it, resulting in a non-superimposable mirror image.

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    Description

    Test your knowledge on the D and L configuration of sugars, and how it is determined based on the orientation of the -OH group on the last chiral carbon. Explore the relationship between glucose, glyceraldehyde, and the rotation of plane polarised light.

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