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Which of the following chair structures represents the highest energy conformation of trans-1-bromo-2-methylcyclohexane? Br Br Br...
Which conformation represents the most stable conformation of trans-1-bromo-4-methylcyclohexane? Br JCH, Br CH, I II сн. III O av
6. Draw both chair conformations of trans-1-bromo-2-methylcyclohexane. Circle the most stable conformation.
Which of the following chair structures represents the lowest energy conformation of cis-1-methyl-2-isopropylcyclohexane?
4. Why does the reaction of trans-1-bromo-2-methylcyclohexane yield the non-Zaitsev elimination product 3-methylcyclohexene on treatment with a base? Draw structures in chair conformations to support your explanation. сн, сн, КОН Br
Draw the most stable conformation for; a. trans-1-chloro-3-methylcyclohexane b. cis-1-ethyl-2-isopropylcyclohexane c. trans-1-bromo-4-ethylcyclohexane d. cis-2-bromo-1-methylcycclohexane Sppecifically, show the ring flipping and calculate the strain using the table given in the power point slides.
Question 9 4 pts Which of the following chair conformations represents the most stable chair conformation of (15,3S)-1-isopropyl-3-methylcyclohexane? n o CY
Dnes the two chair conformations for each of the following compounds and indi zable conformation: cts--tertbutyl-3-methylcyclohexane trans-1-tertbutyl-3-methylcyclohexane cis-1-tertbutyl-4-methylcyclohexane trans-1-tertbutyl-4-methylcyclohexane
Draw the chair conformation of cis-1-bromo-4-chlorocyclohexane in its lowest potential energy conformation.
1. Draw the chair conformation for the following molecules: 이 2. Draw the most stable conformation for the following molecules: a) cis-1-ethyl-3-methylcyclohexane b) trans-1-tert-butyl-4-ethylcyclohexane c) (1R,2R,4S) 2,4-dimethyl-1-isopropylcyclohexane
11. Draw, using chair conformations, the preferred conformations of each of the following. a. trans-1-bromo-4-propylcyclohexane b. cis-1-(1,1-dimethylethyl)-2-methylcyclohexane