1.) Name this molecule and identify and assign a configuration if there are chiral centers.a) (25, TR)-9-chloro-2,7-diethyl nonaneb.) (25, 6R,7R) - 2-chloro-6,7-diethyl-8-methylnonanec.) (2R, 65, 75)-2-chloro- 6,7-diethyl - 8-methyl nonaned.) (25, 65, 75)-9-chloro-3,4-diethyl octane

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Answered: 1.) Name this molecule and identify and…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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3. Determine the relationship for the following pairs of structures. Use "E" for enantiomers, "D" for diastereomers, "C" for constitutional isomers, "S" for same, and "NS" (not same) for different compounds. a. b. с. d. е. f. Н н iPr "Де Br Br OH CH3 CH3 Ή OH OH OH Br Br CH3 CH3 Br -Н НО -Н H3C -ОН COOH Br Br Br Н H3C- Br OH CH3 Н CH3 iPr CH3 Н- -Br НО _H H OH OH CH3 ОН -OH COOH
3. Answer all parts (i-iii). This question relates to the amino acids alanine D and glycine E (structures shown below). H2N- -CH–C: ОН НаN — CH—с—он ČH3 H. D E i) Explain, with reference to their structures, why alanine D is chiral while glycine E achiral. ii) Assign the priority of the substituents present on the chiral carbon of alanine D. Building upon your answer in (ii) draw both the R and S enantiomers of alanine D. In your answer make sure to use "dashes" and "wedges" to indicate the stereochemistry of each enantiomer. ii)
1, part A) We observe 6 carbon stereocenters in the molecule below. Indicate each stereocenter, and give the absolute S or R configuration. 1, part B) Indicate each stereoisomer in this molecule, and give the absolute S or R configuration. Then, indicate E or Z configuration of all alkenes in it (*ignoring aromatic ring*).
Draw the skeletal structure of (S)-hex-5-en-3-ol. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric (chiral) centers, where applicable. Drawing
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Organic Chemistry, Ch.4, WS #2, Stereochemistry - Review of R&S configuration, Fischer Projections, Enantiomers, Diastereomers, Meso Compounds. 1. Assign R or S configuration to each stereocenter. (a) H₂C H₂C a H- H OH CH₂CH₂ - Br CH, (b) 2. For each Fischer Projection, assign R or S configuration. CH₂ CH₂CH₂ b. H₂N- H COOH + -H CH₂ C-OH (c) HTC OH CH₂OH C. Br- CH₂OH CI CHO CH
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Explain your answer. I have the solutions to the questions. The instructor has given us the answer key. I still don't get the professor's answers. It's only the second part of the problem.
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Set C. Some Relatively Easy Molecules (1) SF;CI (2) Chlorobenzene (3) 1,2-Dichlorobenzene (4) 1,3-Dichlorobenzene (5) 1,4-Dichlorobenzene (6) 1,3,5-Trichlorobenzene (7) 1,2,3-Trichlorobenzene (8) 1,2,4-Trichlorobenzene (9) trans-(CrCl,(H,O).J* (ignore H atoms) (10) (11) OPCI, (12) trans-Pt(NH,),Cl; (ignore H atoms) (13) cis-Pt(NH,),Cl, (ignore H atoms) (14) BICIF (15) What is the point group for each of the following substituted cyclo- butanes? Assume that C,H, itself has D symmetry and that replacing an H by X or Y changes no other structure parameters. (a) (d)

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1.) Name this molecule and identify and assign a configuration if there are chiral centers. a) (25, TR)-9-chloro-2,7-diethyl nonane b.) (25, 6R,7R) - 2-chloro-6,7-diethyl-8-methylnonane c.) (2R, 65, 75)-2-chloro- 6,7-diethyl - 8-methyl nonane d.) (25, 65, 75)-9-chloro-3,4-diethyl octane