Consider the e2 elimination of 3‑bromopentane with hydroxide. the starting material consists of a chiral carbon with an in plane bond to bromine pointing to the upper left, an in plane bond to ethyl pointing to the right, a wedged bond to ethyl pointing to the lower left and a dashed bond to hydrogen pointing to the lower left. this reacts with hydroxide to form the product, water and bromide ion. complete the curved arrow electron-pushing mechanism and draw the structure of the organic product formed.
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Consider the e2 elimination of 3‑bromopentane with hydroxide. the starting material consists of a ch...
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