2. Analyze each pair of compounds below. Identify which class of isomers each pair of structures...
Analyze each pair of compounds structures represent. Your cho cach pair of compounds below. Identify which class of isomers each pair of s represent. Your choices are: (i) constitutional, (ii) conformational, (iii) omers, (iv) diastereomer or (v) identical (non-isomers). Only one label for each pair should be used. For each case show work (drawings, (R)/(S), rotation of bonds, chair- "ps, etc) which led you to each answer for the pairs below. Any differences of answers between you and your peers...
6. Which pair of the following compounds are constitutional isomers? A B and C B. A and D C. C and D D. B and D E. A and C 7. Which pair of the following compounds are constitutional isomers? A B and C B. A and D C. C and D D. B and D E A and C 8. Which of the following is a Newman projection for the following compound as viewed down the indicated bond in...
For A, B, C and I and II. It just asks you to draw a pair of examples of the rype of ionomers. isomers. Then, for each class, draw a pair of structures (in bond-line form) to clearly illustrate each class of isomer. Be sure to show proper spatial orientation where needed (often using dash/wedge bonds, or correct double-bond geometry). During your peer review: Did your peers draw correct examples? Suggest improvement if not.] A. Constitutional Isomers (or Structural Isomers)...
Instructions: Read the instructions carefully and answer the following questions in the space provided. Then attach the PDF file on Discussion Board for peer discussion and peer review. 1. In a few sentences define and concisely describe each of the three main classes of isomers below. Configurational Isomers can be further classified as either enantiomers or diastereomers and should also be discussed. Your descriptions should enable your peers to quickly and easily compare and contrast the differences between the different...
7. For each pair of structures shown, indicate whether the two species are constitutional isomers, enantiomers, diastereomers of one another, or identical molecules. (16 pts) . Donna Cat
D. Specify whether each pair of structures below are constitutional isomers, identical, enantiomers, diastereomers or not related. (3 pts) A. ОН ОН Он OH В. ОН но
7. 16 pts Indicate the relationship between each pair of structures listed below by labeling each as either the same, constitutional isomers, enantiomers or diastereomers. Pair of structures Relationship CH H Hairs) diastreamers +2 Hot CO₂H Hgo r H+Bris .COM Constrol ismus o co diesbet diasteamers
4) For each pair of structures, determine if they enantiomers (E), diastereomers (D), or None (N). (12 pts) are identical (I), structural isomers (SI), conformers (C), a) b) Br HJ CH3 Нас. F F Fl Br H CH3 CH3 F F c) d) но но CI 4) Below are Newman projection representations for (2R,3R)-, (2S,3S)- and (2R,3S)- stereoisomers of
please help Identify each pair as identical, conformers, enantiomers, diastereomers, or constitutional isomers. Do not use any designation more than once. (4 pts) CHO B Fisher Projection CHO and BIH CH3 сн. Br- and Br OCH CFS CH' HECH Har BE CF3 and SH and HSH
need help with #2 Enantiomeric pairs: Diastereomeric pairs: Identical molecules: 2. For the structure given below, the name of a specific stereoisomer is given. Show the stereochemistry of the named stereoisomer using a perspective (dash & wedge) structure, a staggered Newman projection and a Fischer projection. (3 pts) он о Y O H (2R,3R)-3-hydroxy-2-nitropentanoic acid NO 7 change ( 3. Decide whether each of the following pairs of structures represent enantiomers, diastereomers, or identical molecules (6 pts) ame one crates