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Concept explainers
(a)
Interpretation:
The name of the given glycoside is to be stated.
Concept introduction:
Glycoside is a class of compounds which are formed when the carbohydrate reacts with alcohol with an acid catalyst such as
(b)
Interpretation:
The products that would be formed when
Concept introduction:
Glycoside is a class of compounds which are formed when the carbohydrate reacts with alcohol with an acid catalyst such as
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Chapter 24 Solutions
EBK ORGANIC CHEMISTRY
- A triglyceride can be optically active if it contains two or more different fatty acids.(a) Draw the structure of an optically active triglyceride containing one equivalent of myristic acid and two equivalentsof oleic acidarrow_forwardDraw the structure of each of the following compounds. an α-N-glycoside formed from D-arabinose and C6H5CH2NH2arrow_forward(a) Provide four distinct forms of phenylalanine. (b) Rank the solubility of these forms in water. (c) Explain your ranking.arrow_forward
- Draw the structure of: (a) a polysaccharide formed by joining D-mannose units in 1→4-β- glycosidic linkages; (b) a polysaccharide formed by joining D-glucose units in 1→6-α- glycosidic linkages. The polysaccharide in (b) is dextran, a component of dental plaque.arrow_forwardIndicate whether each statement is true or false: (a) Fat molecules contain amide bonds. (b) Phosphoplipids can be zwitterions. (c) Phospholipids form bilayers in water in order to have their long hydrophobic tails interact favorably with each other, leaving their polar heads to the aqueous environment.arrow_forwardFrom examination of the molecular models i–v, choose thesubstance that (a) can be hydrolyzed to form a solutioncontaining glucose, (b) is capable of forming a zwitterion,(c) is one of the four bases present in DNA, (d) reacts withan acid to form an ester, (e) is a lipid.arrow_forward
- How glycosidic bonds are formed? Write two real-life application of glycosides and the associated reactions. EXPLAIN.arrow_forwardDraw the structure of an optically active triglyceride containing one equivalent of stearic acid and two equivalents of oleicacid. Draw the products expected when this triglyceride reacts with the following reagents. In each case, predict whetherthe products will be optically active.(a) H2 and a nickel catalyst (b) Br2 in CCl4 (c) hot aqueous NaOH (d) ozone followed by (CH3)2Sarrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
- General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
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