explain why the two stereoisomers of 1,4-dimethylcyclohexane are achiral
Cis-1,2-dimethylcyclohexane and cis-1,4-dimethylcyclohexane have very similar heats of combustion. However, cis-1,2-dimethylcyclohexane is slightly higher. Why?
rank cis-1,2-dimethylcyclohexane, cis-1,3-dimethylcyclohexane and cis-1,4-dimethylcyclohexane in increasing order of stability.
Which, if either, of the 1,4-dimethylcyclohexane isomers shown below is more stable? Explain your answerusing depictions of the relevant conformational equilibria.
Draw the Newman structures for 1,2 dimethycyclohexane , 1,3 dimethylcyclohexane and 1,4 dimethylcyclohexane. Please draw the cis and trans for each. thank you
Predict the percent areas of all of the products ofmonochlorination of 1,4-dimethylcyclohexane.
Which of the following molecules is chiral at room temperature (25 degree C) and why? A.1,1-dimethylcyclohexane B.cis-1,2-dimethylcyclohexane C.trans-1,3- dimethylcyclohexane D, trans- 1,4 - dimethylcyclohexane
Draw the newman projections for 1,4 dimethylcyclohexane for cis and trans with ring flip. there should be 4 newman projections.
Draw 1,4 -Dimethylcyclohexane in hawthorne projection first, then show it in chair conformation in cis then show it flipped. Also, then show it in chair conformation in trans and then show it flipped.
Question 13 (1 point) Is a teapot chiral or achiral? Explain why.
Does 1,3 - dimethylcyclohexane have a higher or lower vapor pressure than water? Please explain why and what factor size has on this situation. I will vote thumbs up for a quick and detailed response. Thanks (: Also, if you could explan why dimethylcyclohexane is not soluble in water, that would be much appreciated!