Answer
Verified
418.2k+ views
Hint: The Haworth projection is simply the three-dimensional perspective of seeing the structure of a molecule represented as the cyclic structure of monosaccharides. More commonly, Fischer projection is converted into the Haworth projection and chair conformation and vice versa.
Complete step-by-step answer:
Let us discuss the concept of Haworth projection in detail;
Haworth projection:
Biochemists often draw the structure of sugars in the form of Fischer projections and Haworth projections. Fischer projection shows the structure in the form of open chains. In this, the carbon atoms of a sugar molecule are connected vertically by solid lines whereas, the carbon-oxygen and carbon-hydrogen is connected by horizontal bonding within them.
This Fischer projection is converted into Haworth projection just by representing itself in the cyclic form. This conversion takes place in some number of steps as described below (specifically for glucose);
We need to rotate the bonds around C-5 clockwise.
Next draw the hexagon omitting the line between OH and CHO.
Further, add $C{{H}_{2}}$ and OH groups to the structure.
Now, connect the line we omitted in step 2 (forming a pyran).
Finally, add the H groups opposite to the OH groups.
Now, as the glucose can exists in two forms (due to the position of H and OH groups on the anomeric carbon); we have shown that as below:
Note: Do note that the Haworth projection can further be converted into chair conformation. But for ease of demonstration many chemists prefer Fischer projection or Haworth projection in general instead of chair conformation.
Complete step-by-step answer:
Let us discuss the concept of Haworth projection in detail;
Haworth projection:
Biochemists often draw the structure of sugars in the form of Fischer projections and Haworth projections. Fischer projection shows the structure in the form of open chains. In this, the carbon atoms of a sugar molecule are connected vertically by solid lines whereas, the carbon-oxygen and carbon-hydrogen is connected by horizontal bonding within them.
This Fischer projection is converted into Haworth projection just by representing itself in the cyclic form. This conversion takes place in some number of steps as described below (specifically for glucose);
We need to rotate the bonds around C-5 clockwise.
Next draw the hexagon omitting the line between OH and CHO.
Further, add $C{{H}_{2}}$ and OH groups to the structure.
Now, connect the line we omitted in step 2 (forming a pyran).
Finally, add the H groups opposite to the OH groups.
Now, as the glucose can exists in two forms (due to the position of H and OH groups on the anomeric carbon); we have shown that as below:
Note: Do note that the Haworth projection can further be converted into chair conformation. But for ease of demonstration many chemists prefer Fischer projection or Haworth projection in general instead of chair conformation.
Recently Updated Pages
10 Examples of Evaporation in Daily Life with Explanations
10 Examples of Diffusion in Everyday Life
1 g of dry green algae absorb 47 times 10 3 moles of class 11 chemistry CBSE
What happens when dilute hydrochloric acid is added class 10 chemistry JEE_Main
What is the meaning of celestial class 10 social science CBSE
What causes groundwater depletion How can it be re class 10 chemistry CBSE
Trending doubts
Fill the blanks with the suitable prepositions 1 The class 9 english CBSE
Which are the Top 10 Largest Countries of the World?
How do you graph the function fx 4x class 9 maths CBSE
Differentiate between homogeneous and heterogeneous class 12 chemistry CBSE
Difference between Prokaryotic cell and Eukaryotic class 11 biology CBSE
Change the following sentences into negative and interrogative class 10 english CBSE
The Equation xxx + 2 is Satisfied when x is Equal to Class 10 Maths
Why is there a time difference of about 5 hours between class 10 social science CBSE
Give 10 examples for herbs , shrubs , climbers , creepers