Hexoses: Difference between revisions
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The figure to the left contains D-glucose drawn as a Fischer projection structure. When drawing a Fischer projection the most oxidized group, in this case the aldehyde group, is positioned at the top, all horizontal bonds project to the front of the plane of the screen and all vertical bonds project behind the plane of the screen. The structure shown to the right in the Jmol applet is drawn in this same conformation, but the structure gives the appearance of being 3D. The applet shows the glucose molecule circling back on itself, so that carbon #6, C-6, (green) circles around to meet the aldehyde carbon, C-1 (orange). Projecting this 3D structure on to a 2D surface gives the Fischer projection structure. In order to observe that the hydroxyl groups on the chiral<ref>[http://en.wikipedia.org/wiki/Chiral_centre Chiral center]</ref> carbons project to the same sides of the carbon chain on the two structures, rotate the Jmol structure upward so that C-1 moves to the back of the screen. When you do that, you will see that the hydroxyl groups on the chiral carbons are on the same sides of the carbon chain as they are in the 2D structure. Compare the structure of the common <scene name='Hexoses/Glucose_sawtooth/1'>saw-tooth conformation</scene> of D-glucose to that of the Fischer projection structure. Toggle off the spin and rotate the molecule so that the hydroxyl group on C-5 is on the right side of the carbon chain. Now, notice the differences in the orientations of the hydroxyl groups on the chiral carbons in the sawtooth conformation compared to those in the Fischer projection. This comparison shows that the saw-tooth conformation can not be used to make the enantiomeric<ref>[http://en.wikipedia.org/wiki/Enantiomer Enantiomer]</ref> assignment. | The figure to the left contains D-glucose drawn as a Fischer projection structure. When drawing a Fischer projection the most oxidized group, in this case the aldehyde group, is positioned at the top, all horizontal bonds project to the front of the plane of the screen and all vertical bonds project behind the plane of the screen. The structure shown to the right in the Jmol applet is drawn in this same conformation, but the structure gives the appearance of being 3D. The applet shows the glucose molecule circling back on itself, so that carbon #6, C-6, (green) circles around to meet the aldehyde carbon, C-1 (orange). Projecting this 3D structure on to a 2D surface gives the Fischer projection structure. In order to observe that the hydroxyl groups on the chiral<ref>[http://en.wikipedia.org/wiki/Chiral_centre Chiral center]</ref> carbons project to the same sides of the carbon chain on the two structures, rotate the Jmol structure upward so that C-1 moves to the back of the screen. When you do that, you will see that the hydroxyl groups on the chiral carbons are on the same sides of the carbon chain as they are in the 2D structure. Compare the structure of the common <scene name='Hexoses/Glucose_sawtooth/1'>saw-tooth conformation</scene> of D-glucose to that of the Fischer projection structure. Toggle off the spin and rotate the molecule so that the hydroxyl group on C-5 is on the right side of the carbon chain. Now, notice the differences in the orientations of the hydroxyl groups on the chiral carbons in the sawtooth conformation compared to those in the Fischer projection. This comparison shows that the saw-tooth conformation can not be used to make the enantiomeric<ref>[http://en.wikipedia.org/wiki/Enantiomer Enantiomer]</ref> assignment. | ||
D-glucose in a <scene name='Hexoses/Glucose_preanomer/4'>conformation</scene> which positions the aldehyde carbon (yellow) so that it can react with the oxygen (green) bonded to C-5 to form a hemiacetal<ref>[http://en.wikipedia.org/wiki/Hemiacetal Hemiacetal]</ref> A result of this reaction is that C-1 becomes chiral, and one of two possible stereoisomers (anomers<ref>[http://en.wikipedia.org/wiki/Anomer Anomer]</ref>) is formed. One anomer, <scene name='Hexoses/Alpha_glucose/1'> | D-glucose in a <scene name='Hexoses/Glucose_preanomer/4'>conformation</scene> which positions the aldehyde carbon (yellow) so that it can react with the oxygen (green) bonded to C-5 to form a hemiacetal<ref>[http://en.wikipedia.org/wiki/Hemiacetal Hemiacetal]</ref> A result of this reaction is that C-1 becomes chiral, and one of two possible stereoisomers (anomers<ref>[http://en.wikipedia.org/wiki/Anomer Anomer]</ref>) is formed. One anomer, <scene name='Hexoses/Alpha_glucose/1'>αalpha-D-glucopyranose</scene> <ref>[http://en.wikipedia.org/wiki/Pyranose Pyranose]</ref> is shown from the perspective of looking on the edge of the structure. This perspective or the Haworth<ref>[http://en.wikipedia.org/wiki/Pyranose#History Haworth projection]</ref> projection is often shown in text books. The anomeric<ref>[http://en.wikipedia.org/wiki/Anomer#Nomenclature Anomeric center]</ref> carbon, C-1 colored orange, is shown on the right side of the structure, its hydroxyl group is projecting down and C-6, not being in the ring, projects up. Notice that, unlike the Haworth projection, the pyranose ring is not planear. The other anomer, <scene name='Hexoses/Beta_glucose/2'>β-D-glucopyranose</scene> is shown. | ||
<Structure load='Open fructose.pdb' size='500' frame='true' align='right' caption='' scene='Hexoses/Open_fructose/3' /> | <Structure load='Open fructose.pdb' size='500' frame='true' align='right' caption='' scene='Hexoses/Open_fructose/3' /> | ||
Revision as of 17:07, 20 March 2013
<StructureSection load= size='450' side='right' scene='Hexoses/Glucose_fischer/3' caption=>
The objective of this article is to illustrate and visualize the structures and concepts of glucose (aldohexose[1]) and fructose (ketohexose[2]) that are difficult to visualize and illustrate by viewing two dimensional structures in textbooks.
GlucoseGlucose
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The figure to the left contains D-glucose drawn as a Fischer projection structure. When drawing a Fischer projection the most oxidized group, in this case the aldehyde group, is positioned at the top, all horizontal bonds project to the front of the plane of the screen and all vertical bonds project behind the plane of the screen. The structure shown to the right in the Jmol applet is drawn in this same conformation, but the structure gives the appearance of being 3D. The applet shows the glucose molecule circling back on itself, so that carbon #6, C-6, (green) circles around to meet the aldehyde carbon, C-1 (orange). Projecting this 3D structure on to a 2D surface gives the Fischer projection structure. In order to observe that the hydroxyl groups on the chiral[3] carbons project to the same sides of the carbon chain on the two structures, rotate the Jmol structure upward so that C-1 moves to the back of the screen. When you do that, you will see that the hydroxyl groups on the chiral carbons are on the same sides of the carbon chain as they are in the 2D structure. Compare the structure of the common of D-glucose to that of the Fischer projection structure. Toggle off the spin and rotate the molecule so that the hydroxyl group on C-5 is on the right side of the carbon chain. Now, notice the differences in the orientations of the hydroxyl groups on the chiral carbons in the sawtooth conformation compared to those in the Fischer projection. This comparison shows that the saw-tooth conformation can not be used to make the enantiomeric[4] assignment.
D-glucose in a which positions the aldehyde carbon (yellow) so that it can react with the oxygen (green) bonded to C-5 to form a hemiacetal[5] A result of this reaction is that C-1 becomes chiral, and one of two possible stereoisomers (anomers[6]) is formed. One anomer, [7] is shown from the perspective of looking on the edge of the structure. This perspective or the Haworth[8] projection is often shown in text books. The anomeric[9] carbon, C-1 colored orange, is shown on the right side of the structure, its hydroxyl group is projecting down and C-6, not being in the ring, projects up. Notice that, unlike the Haworth projection, the pyranose ring is not planear. The other anomer, is shown.
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its structure so that it is positioned similar to α-D-glucopyranose - viewing the front edge of the ring, anomeric carbon is on the right and C-6 projects up. What is the one, and only one, difference in the 3D structures of these two molecules?
FructoseFructose
The applet on the right shows D-fructose in a conformation in which the oxygen of C-5 is in position to react with C-2, the carbonyl carbon, forming a hemiketal[10]. As in the case of glucose forming a hemiacetal, the carbonyl carbon becomes a chiral carbon and an anomeric carbon. The two possible anomers are called α-D-fructofuranose[11] and β-D fructofuranose. The α and β furanoses are shown below.
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The α anomer on the left is shown with an edge-on-view, with the anomeric carbon (C-2) on the right side of the structure and with its hydroxyl group projecting down. C-1 is not part of the five membered ring and projects above the ring. Toggle off the spin of the β anomer on the right and rotate the structure so that it has a position similar to that of the α anomer. Confirm that the configuration about the anomeric carbon of the β anomer is different from that of the α anomer.
Terms Defined in WikipediaTerms Defined in Wikipedia