indicate, with asterisks ("), all of the chirall centers in each of the following molecules. For each molecule, what is the maximum number of stereoisomers that can be formed? H H H as needed. HO H
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Indicate, with asterisks (*), all of the chiral centers in each of the following molecules. For each
molecule, what is the maximum number of stereoisomers that can be formed?
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- B) For each compound below, list the number of chiral centers it contains (dashed box). C) If a compound contains one chiral center, list its groups from highest (1.) to lowest (4.) Cahn-Ingold-Prelog (CIP) priority below the structure. D) In the box below the list, provide the absolute configuration (R) or (S) of each chiral center in the molecule. (If there are zero chiral centers, (R) and (S) have no role). D-NA- 1. 2. 3. 4.B) For each compound below, list the number of chiral centers it contains (dashed box). C) If a compound contains one chiral center, list its groups from highest (1.) to lowest (4.) Cahn-Ingold-Prelog (CIP) priority below the structure. D) In the box below the list, provide the absolute configuration (R) or (S) of each chiral center in the molecule. (If there are zero chiral centers, (R) and (S) have no role). CI 1. 2. 3. 4. 0...B) For each compound below, list the number of chiral centers it contains (dashed box). C) If a compound contains one chiral center, list its groups from highest (1.) to lowest (4.) Cahn-Ingold-Prelog (CIP) priority below the structure. D) In the box below the list, provide the absolute configuration (R) or (S) of each chiral center in the molecule. (If there are zero chiral centers, (R) and (S) have no role). Scroonshot 0... 1. 2. 3. 4. Scroonshot Sorbonchot Screensho roo
- Suppose compounds A and B are enantiomers. What can be said about A and B (select all that apply). a. They are mirror images of eachother b. Neither contains a chiral center c. They consist of the same number & types of atoms d. They are superimposible e. They are NOT superimposable f. They are stereoisomerschiral. If you were able to make another molecule that is a mirror image of the chiral molecule, the mirror image and the original molecule will be non-superimposable. i.e. the atoms surrounding carbon won't completely align. The lack of alignment of the suround atom makes the two molecules different from each other. The central carbon must be surrounded by 4 different groups. The chiral carbon is highlighted. CH;CH) CHICH2 CH3-C-CH2-CHy OH CH) miror The 3D structure of the above molecule focuses on the chiral carbon and the bond surrounding the chiral carbon. The molecule on the left is different from the molecule on the right (mirror image) because they are non-superimposable. H. CH3-C-COOH HOOC COOH CH NH2 NH2 mimor Answer the following questions: 1. Draw five structural isomers for hexane, CHe. Isomer 3 Isomer 2 Isomer 1 Isomer 5 Isomer 4 2. Draw three structural isomers as possible for CHO.[References] Write a structural formula for the lowest-molecular-weight chiral compound that contains C and H, contains only one functional group, and is an alkane. • 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. • Alkene or alkyne groups are not considered to be functional groups for this purpose. H - + O. √n Sn [1 [F ChemDoodle
- view File Edit View Go Tools Screenshot 2023-09... Edited Construct a model of CH₂Cl2 using MolView and answer the following: Can it be superimposed on its mirror image? (Y/N) A/ Is CH₂Cl2 chiral? (Y/N) + Does CH₂Cl2 contain a plane of symmetry? (Y/N) A Window Help 10 minutes remaining A Oh yeah I knowIdentify all the chiral atoms in the below structure by right-clicking a chiral atom to bring up a menu that includes "Atom Properties. Click on "Atom Properties," then click the lock symbol next to the Map field to unlock the field. Enter "1" in the Map field box and click "OK." *Mac users: Use Control-click to access the menu. ▸ View Available Hint(s) L DOCH ¹ CONT? 로 [1] A H₁4] H H-C- H₁ Br H H 'Н Br123 H -H131 H[Review Topics) References] M Identify the absolute configuration of the chirality centers in each of the following compounds as R or S. Note: if multiple chirality centers are present, indicate the stereochemical designations as: RR, SS, RS, or SR (Other terms used for chirality center include chiral center, stereocenter, and stereogenic center.) M MD M CH3 req N. req NH2 req HO2C НО-С 9 more group attempts remaining Retry Entire Group Submit Answer Nes Previous Save and Exit 7:01 PM ) E 10/30/2019
- Check the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the none of the above box under the table. Br HI!... OH Molecule 1 *** H" Br H Molecule 4 OH Br OH Onone of the above Molecule 2 H Br Br ""OH ОН Molecule 5 OH _ H Molecule 3 Br CI H Molecule 6 Br H OH X 5Question 2 Determine whether the molecules below have a mirror image that is the same or different from the original molecule. [answer: same/different] Based on the mirror image, determine whether or not the structure is chiral. [answer: chiral/achiral]. Separate the 2 answers with a comma, no space, e.g., an answer might be same,achiral (C) H H C H H₂C-C-COOH or H analine B Br trant-1,2-dibromocyclopentane OH W H₂C different achiral H NH₂ Does compound A have a mirror image that is the same or different? Is the mirror image chiral or achiral? same,achiral Does compound B have a mirror image that is the same or different? Is the mirror image chiral or achiral? different,achiral Does compound C have a mirror image that is the same or different? Is the mirror image chiral or achiral?2. Butaclamol (at the right) is a potent antipsychotic that has been used clinically in the treatment of schizophrenia. (a) How many stereogenic centers does this compound have as drawn (add an asterisk by those atoms)? acidic solution, the number of stereocenters it possesses changes. What is that number _?) Explain by drawing the functional group (partial structure is fine) that results under acidic conditions? Label all FGs on original structure and the new one that forms under acidic conditions. OH (b) When butaclamol is isolated from an