
Concept explainers
RECALL Define the following terms: polysaccharide, furanose, pyranose, aldose, ketose, glycosidic bond, oligosaccharide, glycoprotein.

Interpretation:
The given terms are to be defined.
Concept introduction:
A long chain of monosaccharides linked by glycosidic bonds is known as a polysaccharide. A five-membered cyclic ring of sugar is furanose and a six-membered cyclic ring is pyranose. A monosaccharide containing an aldehydic group is called an aldose, and if it contains a ketonic group then it is called a ketose. The hydroxyl
Answer to Problem 1RE
Solution:
Polysaccharide: It is a large molecule made up of a large number of monosaccharides that are bound together with glycosidic linkages.
Pyranose: It is a six-membered cyclic sugar consisting of five carbon atoms along with one oxygen atom.
Furanose: It is a five-membered cyclic sugar consisting of four carbon atoms along with one oxygen atom.
Aldose: It is a monosaccharide (a simple sugar) that contains an aldehydic group
Ketose: It is a monosaccharide (a simple sugar) that contains a ketonic group
Glycosidic bond or glycosidic linkage: It is a type of covalent bond that joins one carbohydrate molecule to another carbohydrate molecule.
Oligosaccharide: It is a saccharide polymer that contains a small number of monosaccharides, typically 3–10 monosaccharides molecules.
Glycoproteins: These proteins consist of oligosaccharides that are covalently attached to proteins (or amino acids).
Explanation of Solution
Given information: Polysaccharides, pyranose, furanose, aldose, ketose, glycoside bond, oligosaccharide, and glycoprotein.
Polysaccharide: It is a polymer that consists of a large number of monosaccharides, typically around 20 or more. They are of two types, namely, homopolysaccharides, which consist of a single type of single monosaccharide unit, and heterpolysaccharides, which consist of different monosaccharide units. For example, glycogen, a homopolysacccharide, forms glucose units.
Pyranose: The chemical structure of pyranose contains a six-membered ring, which includes five carbon atoms and one oxygen atom. The formation of pyranose takes place by the reaction of alcoholic group of carbon-5 of an open chain with the aldehydic group of carbon-1 of a similar chain.
Furanose: The chemical structure of furanose contains a five-membered ring that includes four carbon atoms and one oxygen atom. The formation of pyranose takes place by the reaction of alcoholic group of carbon-4 of an open chain with the aldehydic group of carbon-1 of a similar chain.
Aldose: This is a class of carbohydrates that has an aldehydic group and is known as polyhydroxy aldehydes. Aldoses are also called reducing sugars for they act as a reducing agent because of the presence of the aldehydic group. They reduce Tollen’s reagent. For example, glucose.
Ketose: This is a class of carbohydrates that have a ketonic group and is also known as polyhydroxy ketones. They are not reducing sugars but they tautomerize themselves to aldoses before acting as a reducing sugar. For example, fructose
Glycosidic bond: It is a covalent bond that joins a carbohydrate to another carbohydrate or functional group of any other molecule. A substance containing a glycosidic bond is called a glycoside. For example, the glycosidic linkage of two glucose molecules is shown in the following figure:
Oligosaccharides: Such carbohydrates contain 3–10 simple sugars that are linked together. They are naturally found in plants and onions. They are soluble fibers and hence easy to digest. Most common examples are sucrose, maltose, and lactose.
Glycoprotein: It is a type of protein that has a carbohydrate attached to it. This carbohydrate is an oligosaccharide that is covalently attach to a polypeptide chain of protein. It is usually found in aloe vera, brown rice, meat, and so on. They play an important function in the reproduction, immune system, hormone balance, and protection of cells.
All the terms have been defined, along with their structures being described.
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Chapter 16 Solutions
Biochemistry
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- 3. Which one of the compounds below is the major product formed by the reaction sequence shown here? CH3 + CH3NO2 NaOH H2, Ni ? nitromethane acetophenone OH OH HO HN- u x x x x Ph A HO -NH2 HO H Ph Ph Ph N- H B Ph NH2 D Earrow_forward4. Only ONE of the five compounds below can be prepared by an aldol condensation in which a single carbonyl compound is treated with base. Which one is it? To solve this problem, reverse the aldol condensation that formed each of these molecules to find out what two molecules came together to make the products. The one in which the two molecules are identical is the answer. Ph Ph ཚིག གནས ག ནཱ ཀ ན ཀནཱ A Ph H B Ph Ph H D Ph. Ph Ph E Harrow_forward5. Which one is the major organic product obtained from the following reaction sequence? First, equimolar amounts of cyclopentanone and LDA are mixed at -78°C. Then propionaldehyde (propanal) is added. Addition of aqueous acid completes the process. LDA, -78°C. 1. 2. H₂O* H A B H 0 D H H Earrow_forward
- 2. Which one is the major organic product obtained from the following reaction? NaOH, H₂O heat A B C D Earrow_forwardCH3CH2CHO + propanal PhCH2CHO 2-phenylacetaldehyde mixture of four products NaOH 10. In the crossed aldol reaction of propanal and 2-phenylacetaldehyde shown above, a mixture of four products will be formed. Which ONE of the compounds below will NOT be formed in this crossed aldol reaction? OH Ph A H OH OH Ph H B OH OH H H H Ph Ph C Ph D Earrow_forwardAn organic chemist ordered the wrong item. She wanted to obtain 1-hydroxy-2-butanone, butinstead ordered 2-hydroxybutyraldehyde. As a good biochemist, show how the organic chemistcould use biological catalysis to make her desired compound.arrow_forward
- Predict the products of aldolase catalyzing the reaction with acetone and (S)-3-hydroxybutyraldehyde.arrow_forwardA cancer patient undergoing chemotherapy is taking a protein kinase inhibitor drug. The patientis an avid marathon runner and does not want to miss his upcoming race. Is it a good idea forthis patient to attempt a marathon while on this medication? Explain why or why not.arrow_forwardShow the fate of the hydrogen on carbon-2 of glucose.arrow_forward
- BiochemistryBiochemistryISBN:9781305961135Author:Mary K. Campbell, Shawn O. Farrell, Owen M. McDougalPublisher:Cengage Learning
