Identify reagents necessary to convert cyclohexane into 1,3-cylohexadiene: notice that the starting material has no leaving grou
ps and cannot simply be treated with a strong base. you must first introduce functionality into the starting material.
1 answer:
<span>1,3-cylohexadiene i synthesized starting from cyclohexane in following 4 steps.
1) Free Radical Substitution Rxn: Halogenation of cyclohexane in the presence of UV yield chlorocyclohexane.
2) Elimination Rxn: Dehydrohalogenation of chlorocyclohexane yields cyclohexene.
3) Halogenation of Cyclohexene (Electrophillic Addition Rxn) gives 1,2-dihalocyclohexane.
4) Elemination Rxn: When dibromocyclohexane is treated with KOH and heated it gives 1,3-cyclohexadiene as shown below,</span>
1) Free Radical Substitution Rxn: Halogenation of cyclohexane in the presence of UV yield chlorocyclohexane.
2) Elimination Rxn: Dehydrohalogenation of chlorocyclohexane yields cyclohexene.
3) Halogenation of Cyclohexene (Electrophillic Addition Rxn) gives 1,2-dihalocyclohexane.
4) Elemination Rxn: When dibromocyclohexane is treated with KOH and heated it gives 1,3-cyclohexadiene as shown below,</span>
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Answer:
Explanation:
Hello there!
In this case, according to the given information, it turns out necessary for us remember that the first-order kinetics is given by:
Whereas the 27.5% complete means A/Ao=0.275, and thus, we solve for the rate constant as follows:
Then, we plug in the variables to obtain:
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