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rewona [7]
3 years ago
5

Draw the skeletal structure for the monohalogenated alkene formed when trans-1-chloro-4-iodocyclohexane is reacted with 1 equiva

lent of sodium tert-butyl oxide (naoc(ch3)3).

Chemistry
1 answer:
Ksivusya [100]3 years ago
5 0
Because I (iodide) is better leaving group than Cl, so it will leave when this molecule is reacted with strong base (sodium tert-butyl oxide) giving the elimination product provided in picture<span />

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<h3>Stoichiometric calculation</h3>

From the equation of the reaction:

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More on stoichiometric calculation can be found here: brainly.com/question/27287858

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