How can I draw axial and equatorial bonds in glucose?
You follow the steps below.
Step 1. Draw the Fischer projection of glucose.
Step 2. Draw a cyclohexane chair, showing the axial and equatorial bonds.
Replace
Step 3. Insert the
In the Fischer projection their orientations are in the order "right-left-right".
In the pyranose chair, the orientations will be "down-up-down".
Draw the
Draw the
Draw an
The chair form of α-D-glucopyranose is
And the structure of β-D-glucopyranose is
As you move around the β-glucose ring, you see that all the substituents are equatorial.
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Axial bonds in glucose are vertical, pointing up or down, while equatorial bonds are horizontal, pointing outward from the ring. In glucose, the axial position alternates with the equatorial position around the ring.
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When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
- Why is the chair the most stable conformation in the cyclohexanes?
- Why do homodesmotic reactions give more accurate estimates of the intrinsic strain and the cyclic delocalization?
- What is so special about the chair conformation?
- What is the molecular formula for hexane, cyclohexane, and toluene?
- What is the condensed structural formula for cyclohexane?
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