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If a given molecule can exist as stereoisomers draw Fisher projection formula and include in the name R/S.
a) chloroethane
b) chlorobutane
Step by step
Solved in 3 steps with 3 images
- Draw the Newman projection so that it corresponds to the molecule and conformation shown when viewed down the red bond in the direction of the red arrow. Your projection should be oriented as shown by the arrow marked up. So the CH2SH group on the front carbon should be above the H and H3C groups, no matter which template you useDraw the potential energy of the molecule circled at the top. Draw the other 3 Newman projections based on the one already drawn by rotating the back carbon clockwise. Explain your answersdrawn newman projection for most and least stable confirmation and look in direction of arrow. include strains that the least stable conformation has... Is the right side of the molecule an isopropyl?
- Draw both chair confirmations of the substituted cyclohexane drawn below. Be certain to actually do a ring flip. Also be certain to very clearly distinguish axial from equatorial positions. Then circle the more stable conformation. Draw a planar representation of a stereoisomers which would have a higher heat of combustion and lower heat of combustion.( selection lowest energy conformation do all with explanation plz , if u hv already answered earlier do not answer again do not copyfirst box: Draw the missing curved arrow notation. Add lone pairs of electrons and nonzero formal charges. Second Box: Draw the product that will be produced. Be sure to draw in any hydrogen at chiral centers. Add lone pairs of electrons.
- Use flat representation of rings, not chair in the drawing. Determine the most and least stable. Consider the most stable chair for each of these isomers, and then draw the most stable and least stable isomer based on a comparison of the best chair for each one.What would a newman projection look like for A, B, and CQuestion: How many C-types do each of the following compounds have? Label them a, b,c ... And Circle the carbon type that would be the most downfield. Please answer all 4 parts of the question. Thank you!