This is one enantiomer of the molecule. OH H CCH2-CH2-CH3 CH3 Draw the structure of the other enantiomer using wedges and dashes. Click and drag to start drawing a structure.
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- Consider the compound below. a) Draw the structure showing stereochemistry, in which carbon 1 has S configuration and carbon 2 has R configuration. b) Draw the structure showing stereochemistry, in which carbons 1 and 2 have S configuration. c) are the two structures from part a and b diastereomers, identical, enantiomers, or unrelated?1) Circle any of the following characteristics that apply for each molecule and each pair. Label all chiral centers as R or S on the given lines. b. H₂C Br chiral achiral meso Br CH3 H₂C pair of enantiomers, pair of diastereomers, or same molecule chiral achiral Br meso CH3 BrGlucose is a simple sugar with five substituents bonded to a sixmembered ring. a.) Using a chair representation, draw the most stable arrangement of these substituents on the six-membered ring.b.) Convert this representation to one that uses a hexagon with wedges and dashed wedges.c.) Draw a constitutional isomer of glucose.d.) Draw a stereoisomer that has an axial OH group on one carbon
- Compound A is a meso compound. Compounds A and B are enantiomers of each other. Both statements are true. Both statements are false. Only the first statement is true. Only the second statement is true. A B |||||Construct a model in which a tetrahedral carbon atom has four different colored model atoms attached to it- red, green, orange and white representing 4 different atoms attached to the central atom. a) Does the atom have a plane of symmetry? why or why not? b) Now replace the green atom in your model with a second orange atom. Now two of the groups attached to the carbon atom are identical. Does the model now have a plane of symmetry? Describe it. c)A carbon atom has four different groups attached to the stereogenic center. Draw structural formulas for the following compound and mark stereogenic centers with as asterisk: 1-bromobutane, 2-bromobutane, 1,2-dibromobutane, 1,4-dibromobutane, 2,3-dibromobutane.Label each molecule with chiral centers (R) and (S). Which ones have more than one?
- Click on all of the carbon chirality centers in the molecule below. (Other terms used for chirality center include chiral center, stereocenter, and stereogenic center.) If no carbon qualifies, submit your answer without selecting any. H3C. CH3 H3CClick on all of the carbon chirality centers in the molecule below. (Other terms used for chirality center include chiral center, stereocenter, and stereogenic center.) If no carbon qualifies, submit your answer without selecting any. H. CO2H HODraw the following structure and next to it draw its enantiomer. Remember, dots and wedges are needed to convey 3D structure. Br hadi rabe 10 home OH
- Use flat representation of rings, not chair in the drawing. Determine the most and least stable. Consider the most stable chair for each of these isomers, and then draw the most stable and least stable isomer based on a comparison of the best chair for each one.Shown below is Streptomycin, and Neomycin B. Circle and label as many functional groups in these molecules as you can. a. Label each chiral carbon in Streptomycin. How many total stereoisomers exist for Streptomycin? b. Label each chiral carbon in Neomycin B. How many total stereoisomers exist for Neomycin B?Click on all of the carbon chirality centers in the molecule below.