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:
20 g/mol
Explanation:
We can use <em>Graham’s Law of diffusion</em>:
The rate of diffusion (<em>r</em>) of a gas is inversely proportional to the square root of its molar mass (<em>M</em>).
If you have two gases, the ratio of their rates of diffusion is
Squaring both sides, we get
Solve for <em>M</em>₂:
<h2> refer the attachment</h2><h2>If it is correct so mark as brainlest answer!</h2>
