Determine whether the following molecule is chiral. If it is chiral, draw its enantiomer. If it is not chiral, draw a stereoisomer of the compound that is chiral. CH3 CH3
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- Part A Determine whether the following molecule is chiral. It is chiral, draw its enantiomer. It it is not chiral, draw a stereoisomer of the compound that is chiral CH, CH₁Is the following compound chiral, and does it have an enantiomer? Me -Me It is chiral, and it has an enantiomer. It is chiral, but it does not have an enantiomer. It is not chiral, and it does not have an enantiomer. It is not chiral, but it does have an enantiomer.Are the following compounds chiral ? Determine the configuration if it is chiral and draw the enantiomer, for each structure. CH3 OH c) H- CI d) e) Br CI
- 3. Now draw one enantiomer and one diastereomer for each of the following compounds if they have them. One of the compounds is chiral, but you cannot draw enantiomer or diastereomer- why? Br Et Et Br OH OH OH OH1) Which molecule is chiral? Redraw it in the R-configuration. H3C, CH3 CH3 H3C CH3 CH3 H3C H3C CH3 H3C H3C CH3 CH3 `CH3 C D E А В1a. How many stereogenic centers are present 1c. Draw a three-dimensional structure of a in the structure below? Indicate them with asterisk(s). How many stereoisomers stereoisomers are possible? chiral compound with the molecular formula of C4H4Cl₂ that does not have a stereogenic carbon. In addition, draw the enantiomer of this compound. Number of stereogenic centers: Number of stereoisomers possible: 1b. Draw one of the two most stable stereoisomers of the compound in 1a using a planar structure with wedges and dashes. Now draw it in its preferred chair conformation. 1d. Draw two meso compounds with the molecular formula of C7H14.
- Draw a structural formula of the S configuration of the compound shown below. • Use the wedge /hash bond tools to indicate stereochemistry where it exists. Include H atoms at chiral centers only. • Ifa group is achiral, do not use wedged or hashed bonds on it. CH3 CH3 CH;CHCHCN CH,CH,CH,CHCH,CH, CH2NH2 Draw a structural formula of the RS configuration of the compound shown below. Use the wedge /hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. If a group is achiral, do not use wedged or hashed bonds on it. ÇIOlfactory receptors in our noses, used for the detection of odors, are chiral. Therefore, in some cases, we can tell the difference between enantiomers by their odor. Carvone is one such compound that we can distinguish between the R and S enantiomer by their odor. br 1. Identify the chiral center in carvone and draw the R and S enantiomers in the indicated boxes.1. Below is the Fischer projection of a molecule. Is this the (R) or (S) enantiomer? 2. If you swap the positions of the H and the Cl, does this represent the same enantiomer or the opposite one? 3. Having swapped the positions of the H and CI, if you then swap the Cl and methyl group, what happens to the stereochemistry of the chiral center? CH3 H- CI CH,CH3
- Which enantiomer is this molecule? R/R? S/S? R/S? S/R? Give your answer by indicating the configuration of the chiral carbons from left to right on the drawing.1. Draw all possible stereoisomers for the following molecule. Once drawn, assign the configuration at each chiral center as R or S. Give the relationship between each stereoisomer that was drawn as enantiomers, diastereomers, or meso compound. You may build a table to give the relationship between each stereoisomer. ОН NH2Any molecule with two chirality centers is an achiral compound. True or False True False