Consider the molecule 1-tert-butyl-3-methylcyclohexane. These two groups can be cis or trans. Which arrangement is more...
consider the molecule 1-tert-butyl-3-methylcyclohexane.
Consider the molecule 1-lert-butyl-3-methylcyclohexane. These two groups can be cls or trans. Which arrangement is more stable? Answer this question by using wedges and dashes to add the two groups or the cyclohexane template provided.
Question 1.) Which of the following describes the most stable conformation of trans-1-tert-butyl-3-methylcyclohexane? a.) Both groups are equatorial. b.) Both groups are axial. c.) none of these d.) The tert-butyl group is axial and the methyl group is equatorial. e.) The tert-butyl group is equatorial. Question 2.) Alkanes with one to four carbons exists as gases at room temperature. a.) True b.) False Question 3.) How many monochlorination products would be obtained from the chlorination of pentane a.) 1 b.)...
The most stable conformation of cis-1-tert-butyl-4-methylcyclohexane hasA) both groups equatorialB) both groups axialC) the tert-butyl group axial and the methyl equatorialD) the tert-butyl group equatorial and the methyl axial
7. (13 points) For the compound 1-tert-butyl-4-methylcyclohexane: a. Draw the two possible chair conformations for the cis isomer, Which conformation, if either, is more stable? Circle one b. Draw the two possible chair conformations for the cis isomer, Which conformation, if either, is more stable? Circle one trans: C. Between the two more stable isomers circled above, which is more stable? Why?
How would you draw the most stable conformation of trans-1-tert-butyl-3-methylcyclohexane? Axial tert-butyl group on C-1, Axial methyl group on C-3 Equatorial tert-butyl group on C-1, Axial methyl group on C-3 Axial tert-butyl group on C-1, Equatorial methyl group on C-3 Equatorial tert-butyl group on C-1, Equatorial methyl group on C-3 Choices b and care both correct Choices a and d are both correct Submit Answer Tries 0/1 How would you draw the most stable conformation of cis-1-chloro-3-fluorocyclohexane? Axial chlorine on...
Write the two chair conformations of each of the following and in each part designate which conformation would be the more stable: a) cis-1-tert-butyl-3-methylcyclohexane, b) trans-1-tert-butyl-3-methylcyclohexane, c) trans-1-tert-butyl-4-methylcyclohexane, d) cis-1-tert-butyl-4-methylcyclohexane.
Which of the following is the most stable conformation of cis-1-(tert-butyl)-2-methylcyclohexane? Bul But Bul Me Me Me (b) But But But Me Me Me (d) ( e)
How would you draw the most stable conformation of trans-1-tert-butyl-2-methylcyclohexane? O Axial tert-butyl group on C-1, Axial methyl group on C-2 Equatorial tert-butyl group on C-1, Axial methyl group on C-2 O Axial tert-butyl group on C-1, Equatorial methyl group on C-2 O Equatorial tert-butyl group on C-1, Equatorial methyl group on C-2 Choices b and c are both correct Choices a and d are both correct Submit Answer Tries 0/1
Draw most stable chair form for the more stable stereoisomer
for the molecule. All help is appreciated
yclohexane Chair Practice 9. For each of the following do two things: A draw the most stable chair form for the more stable stereoisomer for the molecule B. identify whether the more stable stereoisomer is cis or trans. 7. 1-butyl-2-methylcyclohexane 8. 3-t-butyl-1-methylcyclohexane 9. 1,4-diethylcyclohexane C. For each of the following, do two things: A draw the most stable chair form over groups C...
Explain why 3-methylcyclohexene is more stable than
methylcyclohexane.
ОН HA -H20 2-Methylcyclohexanol cis, and trans) 3-Methyl- 1-Methyl Methylene- cyclohexene cyclohexene cyclohexane