Carbohydrates
An Introduction to General, Organic, and Biological Chemistry ยท 84 exercises
Q. 13.68
What are the differences in the Haworth structures of -D-glucose and -D-glucose? (13.4)
2 step solution
Q. 13.1
What reactants are needed for photosynthesis and respiration?
3 step solution
Q. 13.2
What is the relationship between photosynthesis and respiration?
3 step solution
Q. 13.3
What is a monosaccharide? A disaccharide?
3 step solution
Q. 13.4
What is a polysaccharide?
3 step solution
Q. 13.5
What functional groups are found in all monosaccharides?
3 step solution
Q. 13.6
What is the difference between an aldose and a ketose?
3 step solution
Q. 13.7
What are the functional groups and number of carbons in a ketopentose?
3 step solution
Q. 13.8
What are the functional groups and number of carbons in an aldohexose?
2 step solution
Q. 13.9
Classify each of the following monosaccharides as an aldopentose, ketopentose, aldohexose, or ketohexose:
a. Psicose is present in low amounts in foods.
b. Lyxose is a component of bacterial glycolipids.
5 step solution
Q. 13.10
Classify each of the following monosaccharides as an aldopentose, ketopentose, aldohexose, or ketohexose:
a. A solution of xylose is given to test its absorption by the intestines.
b. Tagatose, found in fruit, is similar in sweetness to sugar.
5 step solution
Q. 13.27
An infant with galactosemia can utilizeglucose in milk but not galactose. How does the Fischer projection ofgalactose differ from that of glucose?
3 step solution
Q. 13.16
Indicate whether each pair of Fischer projections represents enantiomers or identical structures.
8 step solution
Q. 13.11
Identify each of the following structures as chiral or achiral. If chiral, indicate the chiral carbon.
9 step solution
Q. 13.12
Identify each of the following structures as chiral or achiral. If chiral, indicate the chiral carbon.
9 step solution
Q. 13.13
Draw the Fischer Projection for each of the following wedge-dash structures:
7 step solution
Q. 13.14
Draw the Fischer Projection for each of the following wedge-dash structures:
7 step solution
Q. 13.15
Indicate whether each pair of Fisher projections represents enantiomers or identical structures.
9 step solution
Q. 13.19
Identify the chiral carbon in each of the following compounds:
4 step solution
Q. 13.20
4 step solution
Q. 13.17
Identify each of the following as D or L:
6 step solution
Q. 13.18
Identify each of the following as D or L:
6 step solution
Q.13.23
Draw the Fischer projection for the other enantiomer of a to d in problem 13.21.
8 step solution
Q. 13.21
Identify each of the following as the or L enantiomer:
5 step solution
Q. 13.22
Identify each of the following as the D or L enantiomer:
5 step solution
Q. 13.23
Draw the Fischer projection for the other enantiomer of a to d in problem 13.21.
6 step solution
Q. 13. 26
Draw the Fischer projections for -fructose and -fructose.
3 step solution
Q. 13.26
Draw the Fischer projections for D-fructose and L-fructose.
2 step solution
Q. 13.24
Draw the Fischer projection for the other enantiomer of a to d in problem 13.22.
8 step solution
Q. 13.28
Fructose is the sweetest monosaccharide. How does the Fischer projection of -fructose differ from that of D-glucose?
3 step solution
Q. 13.30
Identify a monosaccharide that fits each of the following descriptions:
a. found in high blood levels in diabetes
b. is also called fruit sugar
4 step solution
Q. 13.29
Identify the monosaccharide that fits each of the following descriptions;
a. is also called blood sugar
b. is not metabolizod in a condition known as galactoscmia
4 step solution
Q. 13.25
Draw the Fischer projections for D-glucose and L-glucose.
3 step solution
Q. 13.21
Identify each of the following as the D or L enantiomer:
a. b.
c. d.
8 step solution
Q. 13. 23 Draw the fischer projection of a to d of the following diagram
8 step solution
Q. 13.22
Identify each of the following as D or L enantiomer.
8 step solution
Q. 13.31
What are the kind and number of atoms in the ring portion of the Haworth structure of glucose?
3 step solution
Q. 13.32
What are the kind and number of atoms in the ring portion of the Haworth structure of fructose?
3 step solution
Q. 13.33
Draw the Haworth structures for Glucose and Glucose.
3 step solution
Q. 13.34
Draw the Haworth structures for - and -d fructose.
3 step solution
Q. 13.35
ldentify each of the following as the or isomer.
4 step solution
Q. 13.36
Identify each of the following as the or isomer:
4 step solution
Q. 13.35
Identify each of the following as the or isomer :
4 step solution
Q. 13.38
Draw the Fischer projection for the oxidation and the reduction products of D-mannose. What are the names of the sugar acid and the sugar alcohol produced?
4 step solution
Q. 13.37
Draw the fischer projection for the oxidation and the reduction products of D-xylose. what are the names of sugar acid and the sugar alcohol produced?
2 step solution
Q. 13.39
Draw the Fischer projection for the oxidation and the reduction products of D-arabinose. What are the names of the sugar acid and the sugar alcohol produced?
5 step solution
Q. 13.40
Draw the Fischer projection for the oxidation and the reduction products of D-ribose. What are the names of the sugar acid and the sugar alcohol produced?
5 step solution
Q. 13.44
Indicate whether each disaccharide in the following figure is a reducing sugar or not.
a.
b.
5 step solution
Q. 13.45
Identify the disaccharide that fits each of the following descriptions:
a. ordinary table sugar
b. found in milk and milk products
c. also called malt sugar
d. hydrolysis gives galactose and glucose
8 step solution
Q. 13.46
Identify the disaccharide that fits each of the following descriptions:
a. not a reducing sugar
b. composed of two glucose units
c. also called milk sugar
d. hydrolysis gives glucose and fructose
6 step solution