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- best condition for the reaction (1r,2s)-1 bromo-2methylcyclohexane->(s)3-methylcyclohex-1eneDraw skeletal structures of the following molecules and show the steps: (R)-2-chloro-2-methyloxypentane (2S,3S)-2-bromo-3-chloropentane (1R,2S)-1,2-dibromocyclopentaneOrganic Chemistry HW see image attached Please illustrate on the given image the correct answers - not handwritten Thank you
- iupac nme include stereochemistry if ncessaryone of the chair structures of cis-1-chloro-3-methylcyclohexane is more stable than the other by 15.5 kj/mol (3.7kcal/mo) which is it ? what is the energy cost of a 1,3-diaxial interaction between a chlorine and a methyl group?The reaction CH3-CH=CH-CH3 CH3CH(I)CH(I)CH3 can be achieved with
- for 1-chloro-1-methylcyclopropane + H20 1-methylcyclopropane + HCIThe potential energy of a CH3 group in ethane as it is rotated around the C-C bond can be written V= 1/2V0(1 +cos φ), where φ is the azimuthal angle as shown and V0 = 11.6 kJ mol-1. (a) What is the change in potential energy between the trans and fully eclipsed conformations? (b) Show that for smal lvariations in angle, the torsional (twisting) motion around the C-C bond can be expected to be that of a harmonic oscillator. (d) Estimate the vibrational frequency of this torsional oscil lation.Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This group is called an ethyl group and can be considered a sphere about twice the sizeof a methyl group. Draw the following Newman projections sighting down the C1C2 bond... a. The lowest potential energy conformation. b. The highest potential energy staggered conformation.