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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- How many stereoisomers are possible for the following monosaccharide? a. 4 b. 8 c. 16 d. 2 e. 1Give the molecular and structural formulae for: –2 examples of structural isomers of monosaccharides –3 examples of stereoisomeric monosaccharides. (Do not include glucose, fructose, galactose)(a) What are the two principal polysaccharides in starch? (b) Which of these polysaccharidescontains unbranched chains of the monosaccharides?
- Identify the monosaccharide represented by each of the following structures. Name each compound.Which of the following define the stereochemistry of alanine (as per the structure shown)? Note: Functional groups arranged horizontally are facing towards the front, and the functional groups arranged vertically are facing towards the back. a) d- b) S- c) R- d) I-what is the name of the illustration complex lipids?
- Name the identity of the carbohydrates.Given the structure of disaccharide below: (a) is it reducing? (b) will it react positively with Benedict's reagent and (c) what specific glycosidic linkage is the name of the disaccharide?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. saturated