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Given below is the reagent of a reaction. Predict the products of the following reactions: Indicate NR if there is no reaction.
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- From the data in Figure 4-12 and Table 4-1, estimate the percentages of molecules that have their substituents in an axial orientation for the following compounds: (a) Isopropylcyclohexane (b) Fluorocyclohexane (c) Cyclohexanecarbonitrile, C6H11CNDraw the most stable conformation of pentane, using wedges and dashes to represent bonds coming out of the paper and going behind the paper, respectively.True or False: If you perform a chair flip on cis-1,4-dichlorocyclohexane, the result is still called cis-1,4-dichlorocyclohexane.
- Draw the most stable conformation of 1,4-dichlorobutane, using wedges and dashes to represent bonds coming out of the paper and going behind the paper, respectively.A 1, 2-cis disubstituted cyclohexane, such as cis-1, 2-dichlorocyclohexane, must have one group axial and one group equatorial. Explain.what is the most stable conformation of (1R, 2S, 5R)-1,2,5-trimethylcyclohexane
