4. Which designation of configurations for the stereoisomer of 3-bromomethyl-4-chloro-2-pentanol is correct? CH₁ H- OH H- -CH₂Br H- -CI CH3 A. 2R, 3R, 4R B. 2S, 3S, 4. C. 2R,3S, 4R D. 2S, 3R, 4S E. 2S, 3R, 4R
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PROBLEM 1) Can you explain this problem and solve it correctly, please!
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- up an example (not appearing in this ChemActivity) of a pair of molecules that are a)constitutional isomers, b) conformers. c) configurational stereoisomers.5. Give the stereochemical relationship between each pair of isomers. Examples are same compound (meso), constitutional isomers, enantiomers, and diastereomers. H3C CH3 HO OH lll a. Но OH H Br CH3 b. C/ H3C CI H. ICH3 CH3 с. CH3 H. CH3 d. Но. H3C OH CH2OH Ho CH2OH Br e. Br H3C f. H CH3 H3C CH3Sub-part D,E and F
- Sub-part D, E, and F4. For each of the following molecules, label each stereocenter as R or S. Label the molecules appropriately as chiral or meso. a. b. methionine NH₂ H d. но. OH c. D = 2H, T = ³H, isotopes of hydrogen. f.T. OH OH CI Y ОН5. Draw the structure of (S)-1-bromo-1-chloropropane. Take care to indicate the three- dimensional stereochemistry properly. 6. How many chiral centers does the following compound contain? CH3 7. Label each chiral carbon in the molecule below as having R or S configuration. HO₂C H F. H3C H CH₂CH3
- Describe the stereochemical relationship between the two structures below. H H CHO OH OH CH₂OH I OA Mesomers HO H B. Enantiomers OC. Conformers D. Raceomers E.Diasteromers CHO -H -OH CH₂OH IIimagine attached for question2. Assign the stereochemical configuration of the selected carbon-carbon double bonds (E, Z or N (not a stereocenter)) that are indicated by the arrows. a) HN H,, H3CO HO H H
- Part D. Do the two structures A and B of each pair drawn below represent the same molecule, constitutional isomers, or stereoisomers? If A and B are stereoisomers, further classify them as enantiomers or diastereomers.Draw a structural formula of the RR and RS configuration of the compounds shown below.correct stereoisomers for the reaction