1. Identify the monomer shown above 2. Describe two polymers, i that this monomers can form and the function/ of these polymers
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- Name and encircled the functional group present in the given compound. NOTE: Since only 3 can be answered, please answer the A, B, AND CPlease explain the following terms: Chirality Enantiomer Stereoisomer Diastereomernot a possible value for the number of monosaccharide units in an oligosaccharide?
- 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. saturatedConvert each of the following chair conformations to an open-chain from and to a Fischer projection. Namethe monosaccharides you have drawn.Identify the monomers for the following polymers A.) Maltose B.) Sucrose C.) Lactose
- How many reducing ends and non reducing end does O-a-D-glucopyranofil(l ➔1) a-D-glucopyranoside(a disaccharide) has? Explain with the structure of the disaccharideDraw tripeptide Lys-Thr-Glu at pH 7.4 and circle the six atoms that are restricted in the same plane.How many stereoisomers are possible for the following monosaccharide? a. 4 b. 8 c. 16 d. 2 e. 1