Determine the systematic (IUPAC) name for each of the molecules represented by the Newman projections below. Newman Projection H H Br H H H. H H3C H H CH3 CI CH3 IUPAC Name CH3 ☐ CH3 X show work. don't give Ai generated solution
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- Increased substitution around a bond leads to increased strain. Take the four substituted butanes listed below, for example. For each compound, sight along the C2-C3 bond and draw Newman projections of the most stable and least stable conformations. Use the data in Table 3-5 to assign strain-energy values to each conformation. Which of the eight conformations is most strained? Which is least strained? (a) 2-Methylbutane (b) 2,2-Dimethylbutane (c) 2,3-Dimethylbutane (d) 2,2,3-TrimethylbutaneHere is the chemical structure of 2-bromobutane: Н Η Н Н HHHH C C- C C-H H :Br Η Н .. Decide whether each molecule in the table below is another molecule of 2-bromobutane, a molecule of an isomer of 2-bromobutane, or a molecule of an entirely different compound. molecule CH₂ CH₂-CH₂-CH-Br CH₂ CH₂ -CH₂ Br HI H H H Η H_ H-C- C-C- H-C-H H H relationship to 2-bromobutane (Choose one) (Choose one) Br: a molecule of an isomer of 2-bromobutane ▼Determine the systematic (IUPAC) name for each of the molecules represented by the Newman projections below. Newman Projection IUPAC Name H₂C Br. H -CH3 ☐ H CH3 H. CH3 $ H H H CI H CH3 Br CI HA -H ☐ 0
- O B) II O A) I O D) IV OC) III Question 17 O FLY Which of the following is the correct Newman projection for the following compound as viewed down the indicated bond in the conform CI. H Br CH3 H Br CH3 1 CH3 H CH3 11 H Br CH3 H ||| CH3 Br Η. Bri CH3 CI IV CH3 H CI Br CH3 H H CH3 V1015MSC Chemistry of Biological Systems II Draw both Newman projection and Natta projection of these four molecules. Upload a picture of your drawing below. Watch this video to understand Natta and Newman projections: https://youtu.be/ryHnCOwqTTO Ethane C₂H6 Pentane C5H 12 epis Ethanol C₂H5OH 2-Methylbutane C5H 12 Ø HomI dont know how to find the IUPAC name for these two molecules
- 5. a-G a- Convert the following Newman projection into the bond line structural formula. Must use stereobonds to indicate the orientation of the groups. H3CO CN b- Draw the anti, gauche, and eclipsed conformations of the following molecule using Newman projection. H H H H c- i. Which cyclopropane molecule has the highest torsional strain? ii. Which cyclopropane molecule has the lowest torsional strain? C b aWhich of the following molecules are isomers? (Make sure you can see all of all three structures.) ннн нннн H нн ннн H-C-C-Ċ-Ċ-OH H-C-0-Ċ-Ċ-Ċ-H H-C-C-0-C-C-C-H нннн H ннн нн ннн I II III O , I, and II O I and II I and III Il and III None of the molecules are isomersPlease show reaekson and don't use hend raiting
- Which of the molecules listed could be represented by the following newman projection: 'F H Select one: F O a. F O b. F-F F Ос. .F O d. F• -- H (b) H,C 3-methylhexane CH, (c) B கூ CH, CH, HgCG; சீகூ H₂CH H 3-ethyl-1-methyloctane 3,3 diethyl pentane 5Å, Å,CH, W CH3 CH2 CH₂ W21 Su2... CH3 X -CH3 G b F E L cPlease don't use hend raiting