a) Find a single, simple (me othn funational graup) alkyl halide be readily conveitad into both of thse producto; (aplic is OK) That can one R-X reagont A, 1-bromo-2-methylcyclohexane Treegont B 1- methylcyclohexene (o) 6) Solentify naazent A. e) Sdantefgrangent B tht would minimaie compsting mualeophibe Autratitutions.

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Chapter1: Chemical Foundations
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**3.**

a) Find a single, simple (no other functional group) alkyl halide (cyclic is OK) that can be readily converted into both of these products:

\[ \text{one R-X} \xrightarrow{\text{reagent A}} \text{1-bromo-2-methylcyclohexane} \]

\[ \text{ } \quad \quad \xrightarrow{\text{reagent B}} \text{1-methylcyclohexene \hspace{1em}} (\small{\text{drawing of a hexagon representing the structure}}) \]

b) Identify reagent A.

c) Identify reagent B that would minimize competing nucleophilic substitutions.

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The diagram in part a) consists of a reaction scheme with two paths. The first path is a transformation from "one R-X" to "1-bromo-2-methylcyclohexane" using an unspecified "reagent A". The second path transforms the same "one R-X" reactant to "1-methylcyclohexene" using "reagent B". There is a drawn structure of a cyclohexene, represented as a hexagon.
Transcribed Image Text:Certainly! Here's the transcription of the image for an educational website: --- **3.** a) Find a single, simple (no other functional group) alkyl halide (cyclic is OK) that can be readily converted into both of these products: \[ \text{one R-X} \xrightarrow{\text{reagent A}} \text{1-bromo-2-methylcyclohexane} \] \[ \text{ } \quad \quad \xrightarrow{\text{reagent B}} \text{1-methylcyclohexene \hspace{1em}} (\small{\text{drawing of a hexagon representing the structure}}) \] b) Identify reagent A. c) Identify reagent B that would minimize competing nucleophilic substitutions. --- The diagram in part a) consists of a reaction scheme with two paths. The first path is a transformation from "one R-X" to "1-bromo-2-methylcyclohexane" using an unspecified "reagent A". The second path transforms the same "one R-X" reactant to "1-methylcyclohexene" using "reagent B". There is a drawn structure of a cyclohexene, represented as a hexagon.
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