Identify the chiral carbons in -D-fructose. Identify the appropriate atom by selecting an atom and assigning it a map number of 1. To do this, ri mark to enable the Map field before entering a value. EXP. CONT. но- S CI Br ÓH ÓH P F z O
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- (a) Identify the base and monosaccharide in the following nucleotide. (b) Give the name and three- or four-letter abbreviation for the compound.When a monosaccharide cyclizes, the carbonyl carbon becomes a chiral center. The pair of sterioisomers thus generated is called: tautomers. aptamers. vitamers. epimers. anomers.Identify the monosaccharide below
- Briefly and in simple terms, describe the glycoside bond connecting two monosaccharides in a di- or polysaccharide.Explain the meaning of the designations d and l used to specify the configuration of monosaccharides.Identify the base and sugar in each of the following nucleotides: A. CMP B. dAMP C. dTMP D. UMP
- In the side chain of the amino acid E, there is a carboxylate group attached to the— α-carbon atom. β-carbon atom. γ-carbon atom. δ-carbon atom. ε-carbon atom.Complete the following table by providing the Fischer and Haworth Projections of the given sugars. In the Fischer Projection put an asterisk (*) mark in the chiral centers of the molecule. Sugar Fischer Projection Haworth Projection (Complete) alpha-anomer Haworth Projection (Abbreviated) beta-anomer D-Mannose D-Xylose L-LyxoseComplete the following table by providing the Fischer and Haworth Projections of the given sugars. In the Fischer Projection put an asterisk (*) mark in the chiral centers of the molecule. Sugar Fischer Projection Haworth Projection (Complete) alpha-anomer Haworth Projection (Abbreviated) beta-anomer L-Galactose L-Fructose D-Mannose D-Xylose L-Lyxose