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- Consider the molecules shown here. Assign the R/S configuration to each chiral center.1. Tell whether the following pairs of structures are identical or not. 2. For those pairs that are not identical, explain what types of isomers they are. 3. If there are chiral centers, denote them with the correct R,S.Name the functional groups and circle any chiral centers in these molecules?
- Draw all possible isomers of trimethylcyclopropane. Name them. Which of these isomers are chiral? Indicate by underlining the name(s).IDENTIFY THE CONFIGURATION OF EACH CHIRAL CENTER IN THE FOLLOWING COMPOUNDS.Identify the configuration of the double bond of the given compound. Identify the chiral centers using an asterisk.
- For the compounds shown, use the R/S configuration given in the compound name to finish drawing the structure by changing bonds to the the appropriate wedge‑and‑dash bonds. For each compound, change two of the in‑plane bonds to a wedge and a dashed bond. You can select the chiral bond and click on top of an in‑plane bond to quickly modify it.1. Name and draw all possible isomers of trimethylcyclopropane. Which of the isomers is chiral?2. If this is chiral, then is it an R or S isomer?Mark all chiral carbons with a star in the following molecules.
- A chiral center is a(n) (select all possible answers) atom bearing groups such that interchanging of any two groups leads to a stereoisomer. plane of symmetry so that there are no stereoisomers. tetrahedral atom. enantiomer. non-superimposable mirror image. tetrahedral atom bonded to 4 different substituents.Which objects are asymmetric (have no plane of symmetry): (a) a circular clock face; (b) a football; (c) a dime; (d) a brick; (e) a hammer; (f) a spring?Draw two possible configurations at the given compound's (in the picture) 2 chiral centers.