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Glucose, galactose, and fructose are the most
important monosaccharides.
Fischer Projections of Monosaccharides
Learning Goal Use Fischer projections to draw the
D or L stereoisomers of glucose, galactose, and fructose.
Fischer Projections
A Fischer projection used to represent carbohydrates
• places the most oxidized group at the top
• shows chiral carbons as the intersection of vertical
and horizontal lines
• shows the — H and — OH groups on the horizontal
intersecting line
• places the — CH2OH group at the bottom of the
Fischer projection, which is not chiral
D and L Notations
In a Fischer projection, the — OH group on the
• chiral carbon farthest from the carbonyl group
determines
an L or D isomer
• left is assigned the letter L
• right is assigned the letter D
Core Chemistry Skill Identifying D- and L-Fischer
Projections
D and L Isomers of Monosaccharides
Study Check
In the following Fischer projection of mannose, identify
the monosaccharide as a D or an L isomer.
Solution
In the following Fischer projection of mannose, identify
the monosaccharide as a D or an L isomer.
Need to Identify Procedure
Carbon Chain Number the carbon chain,
starting at the top of the
Fischer projection.
Chiral Carbon Chiral carbon 5 has the
highest number.
Position of — OH The — OH group is drawn
on the right side of carbon
5, which makes it D-mannose.
Mirror Image The — OH groups on the
chiral carbons are drawn on
the opposite side.
ANALYZE
THE
PROBLEM
Solution
In the following Fischer projection of mannose,
identify the monosaccharide as a D or an L isomer.
D-Mannose; the — OH on
carbon 5 is on the right.
Study Check
In the following Fischer projection,
A. identify the number of chiral centers.
B. identify the monosaccharide as a D or an L isomer.
Solution
In the following Fischer projection,
A. identify the number of chiral centers.
B. identify the monosaccharide as a D or an L isomer.
two chiral centers
— OH is on the left;
it is an L isomer.
Glucose and Fructose
D-Glucose is
• found in fruits, corn syrup, and honey
• an aldohexose with the formula C6H12O6
• known as dextrose and blood sugar in the body
• a building block in sucrose, lactose, maltose, and in
polysaccharides such as cellulose and glycogen
D-Fructose, obtained from sucrose, is
• a ketohexose with the formula C6H12O6
• the sweetest of the carbohydrates, twice as sweet as
sucrose
Glucose and Fructose
The sweet taste of honey
comes from the
monosaccharides
D-glucose and D-fructose.
Galactose
D-Galactose
• is an aldohexose, C6H12O6
• is not found free in nature
• is obtained from the disaccharide
lactose
• has a similar structure to glucose
except for the — OH on carbon 4
In a condition called galactosemia, an
enzyme needed to convert galactose to
glucose is missing.
Chemistry Link to Health:
Hyperglycemia and Hypoglycemia
In the body,
• glucose has a normal blood level of 70–90 mg/dL
• a glucose tolerance test measures blood glucose for
several hours after ingesting glucose
Chemistry Link to Health:
Hyperglycemia and Hypoglycemia
Diabetes mellitus can cause hyperglycemia, which
• occurs when the pancreas is unable to produce sufficient
quantities of insulin
• allows glucose levels in the body fluids to rise as high as
350 mg/dL of plasma
Symptoms of diabetes include
• thirst and excessive urination
• increased appetite and weight loss
In older adults, diabetes is sometimes a consequence of
excessive weight gain.
Chemistry Link to Health:
Hyperglycemia and Hypoglycemia
When a person is hypoglycemic,
• the blood glucose level rises and then decreases
rapidly to levels as low as 40 mg/dL
• low blood sugar may occur as a result of an
overproduction of insulin by the pancreas
• symptoms may appear, such as dizziness, general
weakness, and muscle tremors
• a diet may be prescribed that consists of several small
meals high in protein and low in carbohydrates
Study Check
Draw the Fischer projections of D-fructose and L-
fructose.
Solution
Draw the Fischer projections of D-fructose and L-
fructose.
D-Fructose L-Fructose

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Fischer projections of monosaccharides

  • 1. Glucose, galactose, and fructose are the most important monosaccharides. Fischer Projections of Monosaccharides Learning Goal Use Fischer projections to draw the D or L stereoisomers of glucose, galactose, and fructose.
  • 2. Fischer Projections A Fischer projection used to represent carbohydrates • places the most oxidized group at the top • shows chiral carbons as the intersection of vertical and horizontal lines • shows the — H and — OH groups on the horizontal intersecting line • places the — CH2OH group at the bottom of the Fischer projection, which is not chiral
  • 3. D and L Notations In a Fischer projection, the — OH group on the • chiral carbon farthest from the carbonyl group determines an L or D isomer • left is assigned the letter L • right is assigned the letter D Core Chemistry Skill Identifying D- and L-Fischer Projections
  • 4. D and L Isomers of Monosaccharides
  • 5. Study Check In the following Fischer projection of mannose, identify the monosaccharide as a D or an L isomer.
  • 6. Solution In the following Fischer projection of mannose, identify the monosaccharide as a D or an L isomer. Need to Identify Procedure Carbon Chain Number the carbon chain, starting at the top of the Fischer projection. Chiral Carbon Chiral carbon 5 has the highest number. Position of — OH The — OH group is drawn on the right side of carbon 5, which makes it D-mannose. Mirror Image The — OH groups on the chiral carbons are drawn on the opposite side. ANALYZE THE PROBLEM
  • 7. Solution In the following Fischer projection of mannose, identify the monosaccharide as a D or an L isomer. D-Mannose; the — OH on carbon 5 is on the right.
  • 8. Study Check In the following Fischer projection, A. identify the number of chiral centers. B. identify the monosaccharide as a D or an L isomer.
  • 9. Solution In the following Fischer projection, A. identify the number of chiral centers. B. identify the monosaccharide as a D or an L isomer. two chiral centers — OH is on the left; it is an L isomer.
  • 10. Glucose and Fructose D-Glucose is • found in fruits, corn syrup, and honey • an aldohexose with the formula C6H12O6 • known as dextrose and blood sugar in the body • a building block in sucrose, lactose, maltose, and in polysaccharides such as cellulose and glycogen D-Fructose, obtained from sucrose, is • a ketohexose with the formula C6H12O6 • the sweetest of the carbohydrates, twice as sweet as sucrose
  • 11. Glucose and Fructose The sweet taste of honey comes from the monosaccharides D-glucose and D-fructose.
  • 12. Galactose D-Galactose • is an aldohexose, C6H12O6 • is not found free in nature • is obtained from the disaccharide lactose • has a similar structure to glucose except for the — OH on carbon 4 In a condition called galactosemia, an enzyme needed to convert galactose to glucose is missing.
  • 13. Chemistry Link to Health: Hyperglycemia and Hypoglycemia In the body, • glucose has a normal blood level of 70–90 mg/dL • a glucose tolerance test measures blood glucose for several hours after ingesting glucose
  • 14. Chemistry Link to Health: Hyperglycemia and Hypoglycemia Diabetes mellitus can cause hyperglycemia, which • occurs when the pancreas is unable to produce sufficient quantities of insulin • allows glucose levels in the body fluids to rise as high as 350 mg/dL of plasma Symptoms of diabetes include • thirst and excessive urination • increased appetite and weight loss In older adults, diabetes is sometimes a consequence of excessive weight gain.
  • 15. Chemistry Link to Health: Hyperglycemia and Hypoglycemia When a person is hypoglycemic, • the blood glucose level rises and then decreases rapidly to levels as low as 40 mg/dL • low blood sugar may occur as a result of an overproduction of insulin by the pancreas • symptoms may appear, such as dizziness, general weakness, and muscle tremors • a diet may be prescribed that consists of several small meals high in protein and low in carbohydrates
  • 16. Study Check Draw the Fischer projections of D-fructose and L- fructose.
  • 17. Solution Draw the Fischer projections of D-fructose and L- fructose. D-Fructose L-Fructose