Explain why 3-methylcyclohexene is more stable than methylcyclohexane.
Explain why 3-methylcyclohexene is more stable than methylcyclohexane. ОН HA -H20 2-Methylcyclohexanol cis, and trans) 3-Methyl-...
Draw one chair conformation of cis-2-methylcyclohexanol and one chair conformation of trans-2-methylcyclohexanol. Which is more stable?
In each of the cases below, which isomer is more stable? a) 1,4-dimethylcyclohexane (cis/trans?): b) 1-bromo-2-methylcyclohexane : (cis/trans?) c) 1,3-diethylcyclohexane (cis/trans?)
Consider the molecule 1-tert-butyl-3-methylcyclohexane. These two groups can be cis or trans. Which arrangement is more stable? Answer this question by using wedges and dashes to add the two groups on the cyclohexane template provided
i know that trans is more stable than cis but i really
confusion between 2 and 4. please give me the answer with clear
explanation and clear writing.
i dont know anything about bulky group
5. Which of the following is the most stable conformation of trans-1-ethyl-3-methylcyclohexane? CH.CH CH2CH3 ÇH CH3 CH3 CH2CHE CH2CHE - C O (A) 1 (B)2 O(C) 3 O (D) 4
PART B: Cyclohexane Procedures: 1. Make a model of cis-1,2-dimethylcyclohexane and trans-1,2-dimethylcyclohexane. Do a ring flip of both *Draw the two conformation of the cis and trans cyclohexane structures above *List the number of axial and equatorial substituents for both the cis and trans *Which isomer is more stable overall, cis or trans? Why? 2. Make a model cis-1,3-dimethylcyclohexane and trans-1,3-dimethylcyclohexane. Do a ring flip *Draw the two conformation of the cis and trans cyclohexane structures above *List the number...
cis-cyclohexane-1,2-diol is more acidic than trans-cyclohexane-1,2-diol. Based on charge stability, explain why this is the case?
4. Propose two synthetic routes to trans-1-methyl-2-(methylthio)cyclohexane (below) from the starting compound (a) cis-1-chloro-2-methylcyclohexane; (b) trans-1-chloro-2- methylcyclohexane. SCH CH3 5. Rank each of the following groups of substrates in order of decreasing S 2 reactivity. a. b. C. CHỊCH,CH,CI, CHÚCI, (CH, CH) CHOI (CH3),CHCH,CH,Br, (CH3),CHCH,Br, (CH3),CHBr CHỊCH,CI, CH, CH,I, (CH,),CHCl, CH2CH2Br
**WRITTEN WORK** Would the cis or trans isomer be more stable for the following disubstituted cyclohexane? Explain.
**WRITTEN WORK** Would the cis or trans isomer be more stable for the following disubstituted cyclohexane? Explain.
Draw the most stable form of cis-1-Bromo-4-methylcyclohexane and explain why it is the most stable form