a) Use the carbonyl group, number of carbons, and type of stereochemistry (D or L) t classify the following monosaccharides. B CH2OH 0: CHO но -H- HO- Но -H- HOCH2- -HO- HO- ČH,OH ČH2OH i.Compound A is a(n with stereochemistry. ii.Compound B is a(n) with stereochemistry.
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- Assign a name to each of the following monosaccharides. Use D and L designations. H b. CH 2OH a. C=0 C=0 HO-C-H H-C-OH HO-C-H Н-С-Он CH,OH CH 2OH a. b. Circle all chiral centers for the monosaccharides shown. С. d. True or False: The molecules shown can rotate plane polarized light?In the following monosaccharide hemiacetal, identify the anomeric carbon atom. Identify the appropriate atom by selecting an atom and assigning it a map number of 1. To do this, rigl mark to enable the Map field before entering a value. H: 122 EXP" CONT. 0 0 H но OH S Br OH [1] ÓH P. -Which of the following is the correct glycosidic bond linkage of the disaccharide shown? OH но но он Он но но. OH OH O B-(1–1) glycosidic bond O B-(1–6) glycosidic bond O a-(1–6) glycosidic bond O a-(1-1) glycosidic bond
- Classify the following lipid (choose all that apply for the overall structure, not the individual residues). a. wax ester b. fatty acid c. polyunsaturated d. trans alkene(s) e. steroid f. monounsaturated g. triglyceride h. cis alkene(s) i. saturatedIdentify the D,L convention of the following monosaccharidesIdentify the component monosaccharides of each of the following compounds and describe the type of glycosidic linkage in each.
- H HN-C-C-OH H-C-CH, CH2 CH3 The following short passage is about the compound with chemical structure shown above. Use the following word bank to fill in the blanks in the passage. NOTE that some options may be used more than once: functional, L-serine, nonpolar, two, carboxyl, ketone, optimally, hydroxyl, three polar, neutral, methyl, L-isoleucine, four, amino, carbonyl, L-threonine, acidic, one, aldehyde, hydroxide, amine, D-threonine, asymmetrical, optically, D-serine basic, D-isoleucine, 2-hydroxybutanoic acid, L-glutamic acid, five, ionisable active compound with a maximum number of chiral carbon(s) Its is an example of a(n) chemical structure also contains a maximum number of ionisable group(s) at physiological pH. While the presence of a(n) group gives the compound its partial acidic properties group makes this compound nonpolar, the presence of a(n)Draw the following Lipids in: A) Condensed (detailed) Structure B) its Block Diagram.C) Show/Indicate the type of linkages per structure (put an arrow). 1.) Biological Wax (use arachidic acid and a 20-Carbon long chain alcohol to form the ester). Waxes uses saturated fatty acid since it is generally solid at room temperatuesClassify the following lipid (choose all that apply). HO, O wax ester O cis alkene(s) O steroid fatty acid O omega-6 O saturated O monounsaturated O omega-3 O triglyceride O polyunsaturated O trans alkene(s) O O
- d) Consider the following disaccharide C. i. ii. iii. iv. OH HO OH OH HO Disaccharide C OH OH OH Give the IUPAC name for disaccharide C. What is the type of glycosidic linkage. Is disaccharide C a reducing sugar? Does it mutarotate? Explain your answer. What products are formed when disaccharide C is hydrolysed with H3O+.From the following monosaccharides, identify the a anomers. Select all that apply. Select one or more: OH он OH OH O a. OH OH HO но- Ob. ÓH H OH HO но- он H OH O c. HO OH ÓH ÓH d.Draw the structure for an unknown disaccharide using the hints given below: Formed with two glucose monomers. The monomers are linked with a B (1 → 6) glycosidic bond. The disaccharide has an anomeric carbon in the a-configuration.