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- Assign an R or S configuration to the chiral center in each molecule.Assign an R or S configuration to the chiral center in each molecule.Determine and label the configuration of each chiral carbon in the molecule shown below. HN B O FI OH The molecule shown below is the synthetic drug Latuda (Lurasidone) that is prescribed for antipsychotic for the treatment of schizophrenia in adults and adolescents (13-17 years). Examine the molecule carefully and answer the following questions. H 'N (S) H INH (R) (S) (R) IH H (S) O (S) a) Identify and label the functional groups in the molecule. b) Confirm the configuration of each stereogenic (R/S) center the molecule. c) Label the hybridization of all the nitrogen atoms in the molecule d) Circle of the most basic atom in the molecule and estimate the pKa of the conjugate acid of the base.
- Assign R or S configuration to the chirality centers in the molecule below.1.identify the presence of any chiral carbons in your structure by putting a star/highlighting at the appropriate carbon(s). If you have none explain why? 2. identify the presence of an anomeric carbons in your structure by putting a star/highlighting at the appropriate carbon(s). If you have none explain why?2. Assign R and S configurations for each chiral center in the following compound. Draw enantiomers, diastereomers and clearly indicate them. CH3 H C CI Br CH3 H
- Identify each molecule as Chiral or Achiral and write the number of Asymmetric carbons present in each chiral molecules. T) 3 - Chloro- 2- butanol H- -HO- H- -HO- H- -HO- H- -OH ČH2OH U) V)Determine whether each compound is chiral or achiral.There are eight chirality centers in the following molecule. Identify each asymmetric carbon atom by clicking on the circled carbons that are chiral. HO
