
Concept explainers
(a)
Interpretation: The polysaccharides amylopectin, amylose, cellulose, chitin, glycogen, heparin and hyaluronic acid have to be matched with the given glycosidic linkage characterization.
Concept introduction: Glycosidic linkage is a type of covalent bond that joins one carbohydrate to another carbohydrate leading to the formation of disaccharide, oligosaccharides and polysaccharides.
(a)

Answer to Problem 18.163EP
In the polysaccharides amylose, cellulose, chitin and heparin, all the glycosidic linkages are same.
Explanation of Solution
Amylose is an unbranched polysaccharide of starch. The glycosidic linkage present in amylose is
Amylopectin is a branched polysaccharide of starch. The glycosidic linkages present in amylopectin are
Cellulose provides the structural component of plant cell walls. Theglycosidic linkage present incellulose is
Chitin is an unbranchedN-acetyl-d-glucosamine polysaccharide. The glycosidic linkage present in chitin is
Heparin is a type of acidic polysaccharide. It contains the repeating unit of disaccharides. The glycosidic linkage present in heparin is
Hyaluronic acid is a type acidic polysaccharide that is, it has disaccharide as the repeating unit. The glycosidic linkages present in hyaluronic acid are
Glycogen is a starch polysaccharide. It stores glucose in human body and animals. The glycosidic linkage present in glycogen are both
Hence, the polysaccharides amylose, chitin, cellulose and heparin have all the same glycosidic linkages.
(b)
Interpretation: The polysaccharides amylopectin, amylose, cellulose, chitin, glycogen, heparin and hyaluronic acid have to be matched with the given glycosidic linkage characterization.
Concept introduction: Glycosidic linkage is a type of covalent bond that joins one carbohydrate to another carbohydrate leading to the formation of disaccharide, oligosaccharides and polysaccharides.
(b)

Answer to Problem 18.163EP
In the polysaccharides amylopectin and glycogen, some but not all of the linkages are
Explanation of Solution
Amylose is an unbranched polysaccharide of starch. The glycosidic linkage present in amylose is
Amylopectin is a branched polysaccharide of starch. The glycosidic linkages present in amylopectin are
Cellulose provides the structural component of plant cell walls. The glycosidic linkage present in cellulose is
Chitin is an unbranchedN-acetyl-d-glucosamine polysaccharide. The glycosidic linkage present in chitin is
Heparin is a type of acidic polysaccharide. It contains the repeating unit of disaccharides. The glycosidic linkage present in heparin is
Hyaluronic acid is a type acidic polysaccharide that is, it has disaccharide as the repeating unit. The glycosidic linkages present in hyaluronic acid are
Glycogen is a starch polysaccharide. It stores glucose in human body and animals. The glycosidic linkage present in glycogen are both
Hence, the polysaccharides amylopectin and glycogen have some but not all the linkages as
(c)
Interpretation: The polysaccharides amylopectin, amylose, cellulose, chitin, glycogen, heparin and hyaluronic acid have to be matched with the given glycosidic linkage characterization.
Concept introduction: Glycosidic linkage is a type of covalent bond that joins one carbohydrate to another carbohydrate leading to the formation of disaccharide, oligosaccharides and polysaccharides.
(c)

Answer to Problem 18.163EP
In the polysaccharide hyaluronic acid, both
Explanation of Solution
Amylose is an unbranched polysaccharide of starch. The glycosidic linkage present in amylose is
Amylopectin is a branched polysaccharide of starch. The glycosidic linkages present in amylopectin are
Cellulose provides the structural component of plant cell walls. The glycosidic linkage present in cellulose is
Chitin is an unbranchedN-acetyl-d-glucosamine polysaccharide. The glycosidic linkage present in chitin is
Heparin is a type of acidic polysaccharide. It contains the repeating unit of disaccharides. The glycosidic linkage present in heparin is
Hyaluronic acid is a type acidic polysaccharide that is, it has disaccharide as the repeating unit. The glycosidic linkages present in hyaluronic acid are
Glycogen is a starch polysaccharide. It stores glucose in human body and animals. The glycosidic linkage present in glycogen are both
Hence, the polysaccharidehyaluronic acid have both
(d)
Interpretation: The polysaccharides amylopectin, amylose, cellulose, chitin, glycogen, heparin and hyaluronic acid have to be matched with the given glycosidic linkage characterization.
Concept introduction: Glycosidic linkage is a type of covalent bond that joins one carbohydrate to another carbohydrate leading to the formation of disaccharide, oligosaccharides and polysaccharides.
(d)

Answer to Problem 18.163EP
In the polysaccharides heparin and amylose, all the glycosidic linkages are
Explanation of Solution
Amylose is an unbranched polysaccharide of starch. The glycosidic linkage present in amylose is
Amylopectin is a branched polysaccharide of starch. The glycosidic linkages present in amylopectin are
Cellulose provides the structural component of plant cell walls. The glycosidic linkage present in cellulose is
Chitin is an unbranchedN-acetyl-d-glucosamine polysaccharide. The glycosidic linkage present in chitin is
Heparin is a type of acidic polysaccharide. It contains the repeating unit of disaccharides. The glycosidic linkage present in heparin is
Hyaluronic acid is a type acidic polysaccharide that is, it has disaccharide as the repeating unit. The glycosidic linkages present in hyaluronic acid are
Glycogen is a starch polysaccharide. It stores glucose in human body and animals. The glycosidic linkage present in glycogen are both
Hence, the polysaccharides amylose and heparin have all the
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Chapter 18 Solutions
General, Organic, and Biological Chemistry
- 1. Identify the following alkenes as E or Z NH₂ Br 2. Draw the structures based on the IUPAC names (3R,4R)-3-bromo-4-fluoro- 1-hexene (Z)-4-bromo-2-iodo-3-ethyl- 3-heptene تر 3. For the following, predict all possible elimination product(s) and circle the major product. HO H₂SO4 Heat 80 F4 OH H2SO4 Heat 어요 F5 F6 1 A DII 4 F7 F8 F9 % & 5 6 7 * ∞ 8 BAB 3 E R T Y U 9 F D G H J K O A F11 F10arrow_forwardDraw the major product of this reaction. Ignore inorganic byproducts. ○ O 1. H₂O, pyridine 2. neutralizing work-up a N W X 人 Parrow_forward✓ Check the box under each molecule that has a total of five ẞ hydrogens. If none of the molecules fit this description, check the box underneath the table. tab OH CI 0 Br xx Br None of these molecules have a total of five ẞ hydrogens. esc Explanation Check caps lock shift 1 fn control 02 F2 W Q A N #3 S 80 F3 E $ t 01 205 % 5 F5 & 7 © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility FT * 8 R T Y U כ F6 9 FIG F11 F D G H J K L C X V B < N M H option command P H + F12 commandarrow_forward
- Draw the major product of this reaction. Ignore inorganic byproducts and the carboxylic acid side product. O 1. CHзMgBr (excess) 2. H₂O ✓ W X 人arrow_forwardIf cyclopentyl acetaldehyde reacts with NaOH, state the product (formula).arrow_forwardDraw the major product of this reaction. Ignore inorganic byproducts. N S S HgCl2, H2SO4 く 8 W X Parrow_forward
- tab esc く Drawing the After running various experiments, you determine that the mechanism for the following reaction occurs in a step-wise fashion. Br + OH + Using this information, draw the correct mechanism in the space below. 1 Explanation Check F2 F1 @2 Q W A os lock control option T S # 3 80 F3 Br $ 4 0105 % OH2 + Br Add/Remove step X C F5 F6 6 R E T Y 29 & 7 F D G H Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Ce A F7 DII F8 C Ո 8 * 9 4 F10 F C J K L C V Z X B N M H command P ge Coarrow_forwardIndicate compound A that must react with ethylbenzene to obtain 4-ethylbenzene-1-sulfonic acid. 3-bromo-4-ethylbenzene-1-sulfonic acid.arrow_forwardPart 1 of 2 Draw the structure of A, the minor E1 product of the reaction. esc I Skip Part Check H₂O, D 2 A + Click and drag to start drawing a structure. -0- F1 F2 1 2 # 3 Q A 80 F3 W E S D F4 $ 4 % 5 F5 ㅇ F6 R T Y F G X 5 & 7 + Save 2025 McGraw Hill LLC. All Rights Reserved. DII F7 F8 H * C 80 J Z X C V B N 4 F9 6arrow_forward
- File Preview The following is a total synthesis of the pheromone of the western pine beetle. Such syntheses are interesting both because of the organic chemistry, and because of the possibility of using species specific insecticides, rather than broad band insecticides. Provide the reagents for each step. There is some chemistry from our most recent chapter in this synthesis, but other steps are review from earlier chapters. (8 points) COOEt COOEt A C COOEt COOEt COOH B OH OTS CN D E See the last homework set F for assistance on this one. H+, H₂O G OH OH The last step is just nucleophilic addition reactions, taking the ketone to an acetal, intramolecularly. But it is hard to visualize the three dimensional shape as it occurs. Frontalin, pheromone of the western pine beetlearrow_forwardFor the reaction below: 1. Draw all reasonable elimination products to the right of the arrow. 2. In the box below the reaction, redraw any product you expect to be a major product. C Major Product: Check + ◎ + X ง © Cl I F2 80 F3 I σ F4 I F5 NaOH Click and drawing F6 A 2025 McGraw Hill LLC. All Rights E F7 F8 $ # % & 2 3 4 5 6 7 8 Q W E R T Y U A S D F G H Jarrow_forwardCan I please get help with this graph. If you can show exactly where it needs to pass through.arrow_forward
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