20) option e that is (|v) is most stable because isopropyl and ethyl are anti to each other that is far from each other.
21) {||}represent the gauche form because both methyl group are in side of propyl group
22)correct option is c eclipse form are less stable than gauche and anti form
23) (vi) because it is least stable due to eclipsed form and hence highest energy
The Newman Projections below all represent 2,3,3-trimethylhexane. Use them to answer the following four questions H...
The Newman Projections below all represent 2.3.3-trimethylhexane. Use them to answer the following four questions. Η H2 V VI VII VIII 20. Which Newman Projection represents the most stable conformation of 2,3,3-trimethylhexane looking down the 3-4 C-C bond? a. b. c. VIII I VII d. e. III IV 21. Of the options below, which represents the "gauche" conformation of 2,3,3-trimethylhexane down the 2-3 C-C bond? a. II c. VỊ b. V d. I 22. Which answer choice correctly orders the...
CORRECTIONS Name: The Newman Projections below all represent 2.3.3-trimethylhexane. Use them to answer the following four questions. НАН v v VI 20. Which Newman Projection represents the most stable conformation of 2,3,3-trimethylhexane looking down the 3-4 C-C bond? a b. c. VIII I VII d. e. III IV 21. Of the options below, which represents the "gauche" conformation of 2,3,3-trimethylhexane down the 2-3 C-C bond? a. II C. VI b. V d. I 22. Which answer choice correctly orders the...
can you please explain the reasons behind the answers
Is below all represent 2,3,3-trimethylhexane. Use them to answer the following four questions. H VI VII VIII 20. Which Newman Projection represents the most stable conformation of 2,3,3-trimethylhexane looking down the 3-4 C-C bond? a. VIII d. III b. I e. TV c. VII 21. Of the options below, which represents the "gauche" conformation of 2,3,3-trimethylhexane down the 2-3 C-C bond? a. II c. VỊ b. V 22. Which answer choice...
draw the Newman projections. questions 1,2 and 3
1. (1 pts) 1 pts) Draw the Newman projection for the following species, looking down the between (i) ethyl and carboxylic acid group and (ii) OH and carboxylic acid group as the answer). in the bond indicated. Idell as anti, eclipsed or gauche соон OH (1) anti, eclipsed or gauche COOH WH HN (ii) anti, eclipsed or gauche 2. (1 pt.) Which conformation in question 1 is more stable (a) or (b)?...
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...
pt iso 5. (a) For each of the molecules below, draw a Newman projection of the conformation shown. Label any gauche interactions (i) (ii) OH B (b) Draw the Newman projections of the most and least stable conformationns of 3- methylpentane, viewed along the C-C, bond. Label any gauche interactions. example of steric strain or torsional strain? (c) Is a gauche interaction an-
pt iso 5. (a) For each of the molecules below, draw a Newman projection of the conformation...
Understanding Conformation Analysis Draw two Newman Projections for a n-pentane that depict and anti and gauche conformation looking down the c2-c3 bond. Which conformation is the most stable and why?
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)...
3. Consider 2,2,4-trimethylpentane Draw this compound. a. b. Now, provide Newman projections for the three staggered conformations for this compound looking down the C3 - C4 bond. c. Label the orientation of substituents (i.e. gauche or anti) in each structure and circle the most stable conformation(S)
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...