Which is the most stable Newman projection of the molecule below, assuming a Br-CH3 gauche interaction...
Which Newman projection represents the most stable conformation of (CH),CHCH(CH)2? CH3 CH3 СCH3 (B) (A) CH3 H CH3 "СHз CHз CH3 CH3 н CH3 (D) (C) H. tCH3 CH3 CH3 Н Н CH3 CH3
Which Newman projection correctly identifies the HIGHEST energy conformation of the below molecule? Br CH3 • H9C5 Br -Н НХ Х H3C H3CBr НА H9C5 o H3C Br -С5Нэ Н Н H9CsBr -СН3 HTS
7. Draw a wedge and dash structure of the following Newman projection GHz ви HBr CH3 t Br 8. Which of the following is a gauche conformation for butane? Which is the least stable conformation? The most stable? What is the dihedral angle for conformation ? нсна н CH... HOC CH3 сна нен нан, нен нен н" нэн IV 9. What is the IUPAC name of the following compound?
Please provide explainations for your answers. Thanks! 1. Draw 3 contributing resonance structures of the molecule shown. OCH H2N OCH3 A B Which structure do you suppose contributes most? Why? 2. Provide the IUPAC name for the molecule shown below. Br IUPAC name: Ph 3. Draw the 6 Newman projections for the molecule shown, looking down the C(2)-C(3) bond. Circle the Newman projection that you think would be most stable. Use the table of gauche interactions to determine your answer...
'H 22. Given the following table of eclipse and gauche energy values (these are added strains to the molecule). Fill in all 6 newman projects for 2,2,3-trimethylpentane viewed down the C3-C4 bond. Then calculate the total energy of each newman projection and plot them on the graph below. H-H H-Me H-Bu Me-tBu Interaction Gauche Energy (kcal/mol) Eclipse Energy (kcal/mol) Me-Me 0.8 0 2.7 0.5 1.0 8.5 1.3 2.5 3.0 Conformational Energies 360 300 240 180 120 60
Which Newman projection correctly identifies the HIGHEST energy conformation of the below molecule? Br. CH3 H9C5 Br HX H3C H3CBr -H HXH H9C5 CH3C Br -CsH9 H
use a Newman projection of the C3-C4 bond of 223-trimethy1-4-phenylhexane to show the most stable conformation first. Rotate through all of the eclipsed and staggered conformations. Using the energy values provided in the tables below calculate the relative energies of the different conformations. Plot the changes in energy in the graph diagram providd. Hint: Draw a 2D structure first and "bold" the bond viewed in your Newman projection. vided. 2D Structure Approximate Eclipsing Energy Values (kcal/mole) H Me Et i-Pr...
x Consider 2,2,3-trimethylbuttane. Using a Newman projection formula, draw the most stable conformation, sighting along the C2-C3 bond. Compute the total strain energy for this conformation. Refer to strain energy values given below. Strain energies with respect to atoms/groups bonded to C-C (one atom/group bonded to each C) H <---> H eclipsed: 4 kJ/mol CH3 <---> H eclipsed: 6 kJ/mol CH3 <----> CH3 eclipsed: 11 kJ/mol CH3 <----> CH3 gauche staggered: 3.8 kJ/mol Selected Answer: D. 7.6 kJ/mol Answers: A....
4. Draw the most stable E2 elimination product for the following. Include a newman projection justify your answer. (2 points) CH3 - CH₂ a. ČH₂ či H3C- CH b. H. CH₂ (2 points)
4. Draw the most stable and most unstable Newman Projection for the following molecules using the rotation around the C3-C4 bond (use the IUPAC rules to number the chain) 5. Draw the two chair conformations for each of the following cyclohexane derivatives and then choose the conformation that is the most stable. Br BA 3 3 3 $ 2879 So ya 6. For the following compounds, identify the chiral carbons with an asterisk (*) and for those that are not...