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![c) The mixture of D and E would give a specific rotation of [a] = 0°
c. True
d. False](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F23b13ba8-0c65-450d-8dff-f0669c53c193%2F58fb1bf5-1df2-474c-9f39-1e650a6ceebb%2Fvodg1t_processed.jpeg&w=3840&q=75)
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- Provide an appropriate word which may be used to describe a compound with a specific rotation of (a) + 22.5° and (b) -22.5°.7. Determine if cis-trans isomerism is possible for the following compounds. If cis-trans is possible, draw both the cis and the transform. If cis-trans is not possible, explain why. a) isopropylcyclobutane b) 1,2-diethylcyclopropane c) 1-ethyl-1-methylcyclopropaneWhich of the following Newman projections depicts the configuration with the least strain energy. CH CH5 "CHs CHs H3C. CH3 CH3 CH3
- 5. Circle the following molecules that have the R configuration? H. CH,CH,CH,CH, H3C Br --CH,CH, NH2 HC=CH H3C--- H;C CH(CH3)2 H. . 1 3Consider the derivative of cyclohexane A and its representation in chair conformation B: 7 3 H3C $1 Ń 4 9 1 2 Complete Structure B: 3 4 5 6 7 8 9 HO 10 AT Choose... H OH electron lone pair CH3 CH2OH Choose... Choose... Choose... Choose... F Choose... OH ◆ + ♦ ◆ H 10 B 6 5Determine the R and S configurations for the following compounds. (Check placement of lowest priority) *b is a Cl (chlorine) & E has 2 chiral centers-give answer for both HO е. COSH но d. H
- A student isgiven a solution labeled only as 2,3-dihydroxybutane. She used the polarimeter to determine its optical rotation, and found that the solution was not optically active. Draw the absolute configuration of theisomer of 2,3-dihydroxybutane that would give zero optical rotation.I need help with this problem. Draw the rotation or reflection of the XeF4. sigma h of XeF4 and inversion of XeF4. Please draw how you did that.I thought these were both S configuration and it was marked incorrect. Are they both S, or one S and the other R? can someone explain. I think maybe I prioritized each atom incorrectly because I wasnt sure what to do when there were double bonds present