None Determine the systematic (IUPAC) name for each of the molecules represented by the Newman projections below.NewmanProjectionH HBrHHH.HH3CHHCH3CICH3IUPAC NameCH3☐CH3Xshow work. don'tgive Ai generatedsolution

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Answered: Determine the systematic (IUPAC) name…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter4: Organic Compounds: Cycloalkanes And Their Stereochemistry

Section4.SE: Something Extra

Problem 40AP: From the data in Figure 4-12 and Table 4-1, estimate the percentages of molecules that have their...

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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-Trimethylbutane
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 V
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 a
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Nitesh
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
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Provide the IUPAC name for each one
Fqu_5 -. H A dihedral CAqa (o) .el B H ܠܝܢ ܐ ܠܐ ܝܐ ܒܘ ܢܵܐ 14 H H # 14 CI CI H .4 H ww + 0 ub ]8 24 3® 30 4 14 H F H H
Which one of the structures below is the most stable / lowest energy confor of the cis disubstituted-cyclohexane? %3D II IV OII O IV
Organic Chemistry Мaxwell presented by Macmillan Learning Complete the most stable chair conformation of trans-1-tert-butyl-3-methylcyclohexane by filling in the missing atoms. Use the numbering provided on the ring. H Answer Bank 1 H. methyl tert-butyl H H H- 4 3 H H. CO 2.
Q8 Conformational Analysis of Cycloalkanes In this question you will look at the conformations of the following molecule: CH3 C В F CH3 D -E A H3C F I II Energy Costs for Interactions in Alkane Conformers: Computed Energy Cost (kJ/mol)* 3.8 Interaction H+H eclipsed H+CH3 eclipsed CH3+CH3 eclipsed CH3+CH3 gauche H»CH(CH3)2 gauche H CH(CH:)2 eclipsed CH3+CH(CH3)2 gauche CH3+CH(CH3)2 eclipsed HeC(CH:)3 eclipsed CH3+C(CH3)3 gauche CH3+C(CH:)3 eclipsed H+I eclipsed I+CH3 gauche I+CH3 eclipsed "Values computed with Gaussian09 using B3LYP/6-31G(d) for structure optimization and B3LYP/6-311+G(2df,3p) for the conformation energy. The calculations were performed in the gas phase (no solvent). *This result for t-butyl is a bit peculiar given that the value is less than that for isopropyl, but there is an explanation that I can tell you about in office hours! 4.8 12.6 3.7 (0.0) 3.1 3.6 17.3 2.8 13.6 18.7 6.7 1.2 15.5 Steric Strain in Monosubstituted Cyclohexanes: 1,3-Diaxial strain Y (kJ/mol)…

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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