2. (10 points) For the following molecule: Cl Cl (a) Provide the IUPAC name for the...
OCH3 3. Indicate the electrophilic or nucleophilic centers for the following compounds: a) b) d) 4. Answer the following questions regarding 2,3-dimethylbutane: a) draw any staggered Newman projection of this compound looking down the C2-C3 bond. b) draw the highest energy conformation (as a Newman projection). Label each example of steric and/or torsional strain. c) draw the lowest energy conformation. Identify any sources of steric or torsional strain if present. m md iminetahm 5 Draw tra possiblechair conformatex For Jbrom-s-7ethiTmethychayo...
2. Consider the C2-C3 bond in n-pentane: a. Draw a Newman projection for the molecule. b. Show its most unstable conformation. c. Show its most stable conformation. d. Show one gauche conformation.
1. a) Calculate the lowest energy conformer of 2-methylpropane. Use as many calculations as necessary. Then, draw the Newman projection looking down the C1-C2 bond and draw it with 3-D geometry. b) Calculate the lowest energy conformer of 2-methylbutane. Use as many calculations as necessary. Then, draw the Newman projection looking down the C2-C3 bond and draw it with 3-D geometry.
Conformations of the 1 - bromopropane molecule: Draw the line-bond structure of the 1-bromopropane molecule (C_3 H_7 Br). You will draw your Newman projection based on the rotation of the bond between the first and second carbon atoms (C1-C2). Highlight this carbon-carbon bond by drawing the bond as a bold line. Next, use your model kit to build a model of the molecule. Draw the Newman projection for each dihedral angle at 60 degree interval (from 0 degree to 360...
18. How many rings does the following molecule have? AL B.2 0.3 0.4 E. None of the above 19. Which of the following would represent the lowest energy conformation of butane looking at the Newman projection down the C2-C3 bond? A. The (CH3,CH3) eclipsed conformation C. The gauche conformation B. The (H,CH) eclipsed conformation D. The anti-conformation E. The parallel conformation
ох 1. Provide the name of the following compounds. så stk 2. Provide the name of the following compounds. 3. Provide the line structure given the following names. A. 2,6,6,8-tetramethyl-5-neopentyldecane R. 7-methylbicycln[4.2.2]decane ох 4. A. Draw the Newman Projection of pentane looking down the C2-C3 bond in a stageered confirmation B. Draw an energy diagram showing the conformational analysis using the Newman Projection above (showing a 360 degree total rotation, 60 degrees at a time). Hint - see Figure 46,...
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...
CUI 2 1) Give the IUPAC name corresponding to the following structure: 2) Draw the Newman projection formula for the most stable conformation of the C2-C3 bond in 3-methylpentane. [3]
I need to know if my newman projections are labeled and drawn correctly TH rele all 2º carbons in the following molecule. (1 pt) 2 6-iso prop the molecule drawn below: a. Draw a Newman projection looking down the C3 to C2 bond. (2 pts) b. Draw the highest energy conformation looking down the C3-C2 bond (1 pts) Me t me B. Me H Me HO (22 6330 H 4 5 (GHS и a. Newman Projection b. Highest Energy ich...
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)...