Between the cis and trans configuration of 1-chloro-3-methylcyclohexane, which is the most stable stereoisomer and configuration? To prove your argument, use your models or a modelling software to model cis- and trans-1-chloro-3-methylcyclohexane (show all the hydrogens and ensure proper chair conformation) and use arrows to show where steric strain occurs. Include these photos in your answer.

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A:

Q: a) b) c) CHO H- -NH₂ HO-H CH₂OH H CH3 o H H CH3 Ph H I J CI -I H I I H- CH₂OH -OH -NH₂ CHO H3C H Ph…

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Q: Cyclohexane derivatives exist primarily in the most stable of the available chair conformations.…

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Q: C. Using your molecular modeling kit, construct cis-1,4-dimethylcyclohexane. In the space below,…

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Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.