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- Predicting most stable conformer for Newman projections (What if there three different groups? Which one should be anti to each other? The largest one?) Can you explain it and provide examples pleaseFinding strain energy confusedLeast stable conformer of 2,3-dicholorbutane in Newman projection form.
- PayalMonosubstituted cyclohexanes occur in two equilibrium conformations. In one conformation, the substituent is in an axial position. In the other conformation, the substituent is in the equatorial position. Complete the drawing of each chair conformation below and circle the more stable conformation.Which of conformations in the options is a correct conformation of the following molecule and has the lowest energy? O CH3 CH3 it CH3 H3C CH3 CH3 CH3 CH3 CH3 H3C CH3 CH3
- Draw the conformations of pentane using a Newman projection of the view along the C2-C3 bond. Identify the least stable conformation.starting from the wedge and dash structure below, rotate the back carbon to provide the newman projection in the least stable conformationMonosubstituted cyclohexanes occur in two equilibrium conformations. In one conformation, the substituent is in an axial position. In the other conformation, the substituent is in the equatorial position. Complete the drawing of each chair conformation below and circle the more stable conformation. Br
- NO Consider the molecule below: H₂C H3C CH₂CH3 CH₂CH3 Consider rotation around the indicated bond. [1] Draw a Newman projection for the lowest energy conformer of this molecule looking down the indicated bond. [2] Draw a Newman projection for the highest energy conformer of this molecule looking down the indicated bond. # 3 d F4 % 5 F6 00Sighting down the Ci-C2 bond axis of 1-bromopentane, Br-CH2-CH2CH2CH»CH3, draw the Newman projection of a) the anti staggered conformation b) the gauche staggered conformation c) the two eclipsed conformations. Which eclipsed structure would you expect to have the highest strain energy?87. Subject :- Chemistry
