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- rotation here a. Draw the three staggered and three eclipsed conformations that result from rotation around the designated bond using Newman projections. b. Label the most stable and least stable conformation. CH3-C-CH,CH31. Provide proper IUPAC names for the following compounds. a. CH3 | CH3C CCHCH2CH2CH3 CH3 Br b. H₂C=CH-C-CH-CC-H | CH3 C.which c-h bond has the lowest BDE (bond disassociation energy)?
- 4. Circle any n-conjugated portions in the molecules below. Draw all resonance structures for each conjugated molecule. OCH3 H2C=CH-C=N CH3 CH2 H2CConvert each three-dimensional model to a Newman projection around the indicated bond.The following Newman projection corresponds to what IUPAC name? H H. .CH2CH3 CH3CH2 H. H
- Consider 1,2-dimethylcyclohexane. a.Draw structures for the cis and trans isomers using a hexagon for the sixmembered ring. b. Draw the two possible chair conformations for the cis isomer. Which conformation, if either, is more stable? c. Draw the two possible chair conformations for the trans isomer. Which conformation, if either, is more stable? d.Which isomer, cis or trans, is more stable and why?draw newman projection for the indicated bond. put largest groups anti to each other.a.Draw the most stable conformation of trans-1,2-dimethylcyclohexane. b. Draw the most stable conformation of cis-1,2-dimethylcyclohexane.