can you show how you got the anwser for both set by step Draw Newman projections looking down the C3 to C4 bond of (...
Draw Newman projections of 2, 3-dimethylbutane, looking down the C2 to C3 bond, in the most and least stable conformations. Label any important interactions.
Draw Newman projections (looking down the C2-C3 bond) of the three staggered conformers of 2-methylbutane. Rank the conformers in order of increasing energy. Justify your rankings. pls & thx
Draw a newman projection of the most stable staggered conformation of 4-bromo-3-methylheptane looking down the C3-C4 bond. Then draw a newman projection of the least stable staggered conformation of the same compound looking down the C3-C4 bond - label where different type(s) of strain occur making this conformation less stable? I have no idea how to do this so step by step would be perfect. Thank you.
6. Conformational Analysis: Newman Projections (25 points) Consider the rotation around the C3-C4 bond of (3R 4R)-3,4-dibromohexane. C3-C4 bond. B Draw all three eclipsed Newman projections. In no particular order. Calculate the total strain associated with each conformation using the table below, enter on the provided line, and identify the least stable conformation (Circle it) Briefly explain your assignment of the least stable conformation - including which specific types of steric strain are involved. Short phrases are great complete sentences...
draw the skeletal formula and newman projections for following: Look down (2 to C3 bond of (28,35, 55)-3,5-dimethylheptan-2-01
Draw the potential energy diagram for heptane upon rotation (of the C3-C4 bond) every 60 degrees. Label the x-axis "Rotation" and the y- axis "Potential Energy". Show the molecule in a Newman projection looking down the C3-C4 bond and draw each projection at the corresponding local maxima and minima. 8. Draw all structure of the isomer of CeH14 that only has primary and tertiary carbons. (3 points) 9. Draw the Potenti every 60 degrees, I ergy diagram for heptane (i.e....
16. Draw the Newman projection (viewing down the C3-C4 bond) for the two staggered conformations of hexane that have different energies. Indicate the conformation with the lowest energy. (5 pts) 17. Consider the molecule below. (10 pts) CZ Bry Br CI a) Is this molecule chiral? Provide an explanation. b) Draw both chair configurations for this molecule, and circle the more stable conformation (if applicable).
Draw Newman Projections for 360 rotation around C3-C4 bond of 3-isopropylhexane. Label each structure as totally eclipsed eclipsed, gauche or anti. Estimate the relative energy of each structure and draw the potential energy diagram | QUESTION 6 Complete the following acid-base reaction and estimate the equilibrium constant: 2 он H2C H2 H2 QUESTION 7 If a solution of a pair of enantiomers has a measured rotation of +15°, and the pure S enantiomer has a specific rotation of +25°, what...
Can you explain these 2 especially how you will know the leaving groups... please only answer if you know the correct answer. I will rate 3. Predict the major product for the following elimination reaction. Make sure that you draw any relevant Newman projections (looking down the C3-C4 bond) to support your answer. КО-Bu Hас" ён, t-BuOH 1 Draw a dibromide with molecular formula Ci4H12Br2 that would give exclusively the following alkene 4. under E2 reaction conditions. Use wedges and/or...
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...