Draw the most and least stable conformation of 2,4-dimethylheptane as a wedge-dash structure down the C3-C4bond...
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.
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?
3. (a) A bond-line (dash/wedge) structure for butane is shown below. Using the Newman projection templates provided, draw the overall lowest energy (most stable) and overall highest energy (least stable) conformation possible in Newman projection form sighting down the bond indicated. Provide a brie explanation to justify the conformer shown for cach case. (2pts each correct Newman, 2pts for valid explanation) sight down CG- bond Lowest Energy (most stable) Highest Energy (least stable) Explain: (b) For the bond-line structure below...
1. Draw the dash-wedge structure that corresponds to the following Newman proje OH Htci CH CH3 4 Label each stereocenter in the following molecule with an asterisk (*) and identity it as na configuration. molecule with an asterisk (*) and identify it as having an R or an S NH2 3. Draw the most stable chair conformation for the following molecule. 4. Draw 3-ethoxypentane. 5. Assign the priority of the substituents around the asymmetric carbon. Br H I BY BE
that represents the most and the least stable conformation of 3,3- 3) Draw the Newman projection the dimethylhexane viewed along the C3-C4 bond. (3pts)
3. 1) Draw the Newman projection of the following compound, looking down the indicated bond. (2) Label this Newman projections as a staggered or eclijpsed conformation. (3) Rotate this Newman projection to draw the Newman projection of the most stable conformation of this compound. (3) Label this Newman projections as a staggered or eclipsed conformation. (4) Re-draw this most stable conformation in a wedge-dash form as the original compound below is shown). a. он в н b. Cl 3. 1)...
how to draw wedge dash structure and newman projection for C2-C3 bond for 3-bromo-2,2,3-trichloro-1-fluorobutane
осс Стриотсуттогасити рта 9 часосото. Draw a wedge-and-dash structure of the lowest energy anti-gauche conformation of pentane. Explicitly draw out ALL hydrogen atoms on the first 4 carbons. Draw the last CH3 without explicitly drawing out its 3 hydrogen atoms. Edit
1. Draw the Neman Projection of the following Promane descriptions Newman projection for most stable Newman projection for least stable conformation conformation 2. Draw the Newman projections for butane looking down the C2-C3 bond through a full 360 degree rotation. Start with the anti-staggered Newman projection then draw and label each Newman projection (staggered, eclipsed, gauche, anti-staggered, fully-eclipsed) for every 60 degrees of rotation Newman projection for most stable Newman projection for second-most stable conformation Conformation Newman projection for least...
how to draw wedge dash structure and newan projection for C2-C3 and C5-C6 bond for (1R,2R,3R,5S)5-bromo-2-chloro-3-ethyl-5-methylcyclohexanol