Draw theSawhorsee and newman projections of trans 1,3 dibromo cyclohexane in chair form. Please include how you went from chair formation to sawhorse formation and then to new projection
While drawing Newman projection you have to go through sawhorse. And the substituted groups should be in the consecutive position through which you will see the C-atoms so that the upper and lower carbon dont bear those substituted groups (here Br). Because then you would not be able to show their cis and trans positioning.
Draw theSawhorsee and newman projections of trans 1,3 dibromo cyclohexane in chair form. Please include how...
Draw newman projections of 1-2 cyclohexane and 1-3 cyclohexane cis and trans. there should be 8 total newman projections. 1,2 and 1,3 dimethylcyclohexane is what it is supposed to be The 8 newman projections include ringflips of cis and trans.
5. Construct a model of 1,2-difluoroethane. Draw the Newman projections for the staggered and eclipsed conformations of 1,2-difluoroethane. Are these molecules isomers or conformers? If they are isomers to what specific category do they belong? 6. The structure of cyclohexane (C6H12) is based on a six membered ring of carbon atoms. Construct a model of cyclohexane. Cyclohexane can exist in two conformations; the boat or chair conformation (shown below). What are the C-C-C, C-C-H, and H-C-H bond angles at each...
1. Draw (1S,3S)-3-aminocyclohexanecarbonitrile structure below: 2. Draw the two chair conformations of the above disubstituted cyclohexane compound, before and after ring-flip. 3. Draw the Newman projections of both chair conformations about the C1−C6 and C3−C4 bonds. 4. Which conformation is the least stable one? Briefly explain your answer with words AND by showing it on the appropriate Newman projection.
2.16. Using a Newman projection, draw a staggered and eclipsed 2.17. For alkanes containing four or more carbons, use the Newman projection to draw 2.18. Describe what contributes to the changes in the potential energy of an alkane as you on of an alkane. (Section 4.7) the gauche and anti conformations. (Section 4.8) rotate around a carbon-carbon bond. (Section 4.7 & 4.8) energy conformations. (Section 4.7 &4.8) carbon bond. (Section 4.7 & 4.8) 2.19. Use a sawhorse projection or Newman...
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)?...
Draw the Newman structures for 1,2 dimethycyclohexane , 1,3 dimethylcyclohexane and 1,4 dimethylcyclohexane. Please draw the cis and trans for each. thank you
1. (a) Different conformations are found in pentane. (i) Using Newman Projection, draw all the possible staggered and eclipsed conformations of pentane by referring to the bond rotation at C2-C3. (ii) Compare their stability and explain your answer. (b) Draw the most stable form of the chair conformers for trans- and cis-1,4-dimethyl cyclohexane. Comment on their stability. thanks
6) (10 Pts) Draw the most stable and the least stable Newman projection for the following molecule looking down the indicated bond. Most Stable Least Stable 7) (16 Pts) Draw the most stable and the least stable chair form for the molecule below. You must also draw the Newman projection for both chair conformations looking from the direction indicated by the arrows. More stable chair Newman Projection -more stable chair less stable chair Newman Projection -less stable chair 6) (10...
please draw (trans)1,3-dimethylcyclohexane in the most stable chair conformation, and assign-EXPLAIN the stereochemistry to each chiral center.. (why S or R, assign priorities)