AQA · A-Level · Biology

    Course version: 7402 · Version from Sept 2016

    Glucose has two isomers, α-glucose and β-glucose, with structures:…

    Full specification wording

    Carbohydrates: Glucose has two isomers, α-glucose and β-glucose, with structures: Polysaccharides are formed by the condensation of many glucose units.

    Alpha-glucose and beta-glucose are isomers: both are C₆H₁₂O₆ built on the same six-membered ring, and they differ only at carbon 1, where the positions of the hydrogen atom and the hydroxyl group…

    Checked against the AQA 7402 specification (opens in a new tab) on .

    • Point 4 of 8
    • 4 key terms

    Study notes

    From the checked teaching notes for this specification point.

    The idea

    Alpha-glucose and beta-glucose are isomers: both are C₆H₁₂O₆ built on the same six-membered ring, and they differ only at carbon 1, where the positions of the hydrogen atom and the hydroxyl group are inverted. In alpha-glucose the hydroxyl group on carbon 1 sits below the ring; in beta-glucose it sits above. That single difference decides which polysaccharide can be built and what it is good for. Joining many glucose units by condensation gives a polysaccharide, with one glycosidic bond formed and one water molecule released per join. With alpha-glucose the hydroxyl groups line up directly, so the chain can coil into a helix or carry branches, giving amylose, amylopectin and glycogen. With beta-glucose the hydroxyl groups only align if alternate molecules are rotated through 180 degrees, so the chain is forced straight and unbranched, giving cellulose.

    What earns the marks

    • Stating that alpha-glucose and beta-glucose have the same molecular formula but a different arrangement of atoms.
    • Identifying the difference as the inverted positions of the hydrogen and hydroxyl groups on carbon atom 1.
    • Stating that many glucose units join by condensation, forming glycosidic bonds, to make a polysaccharide.
    • Linking alpha-glucose to starch and glycogen and beta-glucose to cellulose.
    • Stating that alternate beta-glucose molecules are rotated 180 degrees in the chain.

    Common mistakes and how to put them right

    • Claiming the two isomers have different molecular formulae or different numbers of carbon atoms.

    • Naming the wrong carbon, most often carbon 4, as the one where the groups are inverted.

    • Answering 'they are different shapes' with no reference to the hydroxyl group position.

    • Stating that beta-glucose cannot form glycosidic bonds at all, rather than needing rotation first.

    • Labelling a diagram without indicating which carbon is carbon 1.

    Exam tips

    • Number the carbons on any glucose diagram before you answer - carbon 1 is the one to the right of the ring oxygen.
    • Use the word inverted or reversed about the hydrogen and hydroxyl groups; it is the phrasing the mark scheme rewards.
    • Explain the consequence as well as the difference: alpha allows coiling and branching, beta forces a straight chain.

    Try the lesson

    The start of the Carbohydrates: Glucose has two isomers, α-glucose and β-glucose, with structures: Polysaccharides are formed by the condensation of many glucose units. lesson, made from checked teaching notes for this specification point.

    Have a go first

    Which of the following are the two isomers of glucose?

    Listen

    Alpha-glucose and beta-glucose are isomers: both are C₆H₁₂O₆ built on the same six-membered ring, and they differ only at carbon 1, where the positions of the hydrogen atom and the hydroxyl group are inverted. In alpha-glucose the hydroxyl group on carbon 1 sits below the ring; in beta-glucose it sits above. That single difference decides which polysaccharide can be built and what it is good for. Joining many glucose units by condensation gives a polysaccharide, with one glycosidic bond formed and one water molecule released per join. With alpha-glucose the hydroxyl groups line up directly, so the chain can coil into a helix or carry branches, giving amylose, amylopectin and glycogen. With beta-glucose the hydroxyl groups only align if alternate molecules are rotated through 180 degrees, so the chain is forced straight and unbranched, giving cellulose. A strong answer earns marks for these points. stating that alpha-glucose and beta-glucose have the same molecular formula but a different arrangement of atoms. identifying the difference as the inverted positions of the hydrogen and hydroxyl groups on carbon atom 1. stating that many glucose units join by condensation, forming glycosidic bonds, to make a polysaccharide. linking alpha-glucose to starch and glycogen and beta-glucose to cellulose. Exam tip: Number the carbons on any glucose diagram before you answer - carbon 1 is the one to the right of the ring oxygen.

    Key words

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    isomers of glucose

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    carbon 1 inversion

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    condensation of many glucose units

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    structure determines polysaccharide

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    See every definition
    isomers of glucose
    Alpha-glucose and beta-glucose have the same molecular formula but a different arrangement of atoms.
    carbon 1 inversion
    The positions of the hydrogen atom and the hydroxyl group on carbon 1 are inverted between the two isomers.
    condensation of many glucose units
    Many glucose units join by condensation, with one glycosidic bond formed and one water molecule released per join, to make a polysaccharide.
    structure determines polysaccharide
    Alpha-glucose allows coiling and branching, giving amylose, amylopectin and glycogen, while beta-glucose forces a straight and unbranched chain, giving cellulose.

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