Questions and Answers of Organic Chemistry

When the following optically active alcohol is treated with HBr, a racemic mixture of alkyl bromides is obtained:Draw the mechanism of the reaction, and explain the stereochemical outcome. Br Он
Draw resonance structures for each of the following compounds:a.b.c.d.e.f.g.h.i.j. N.
There are three constitutional isomers with the molecular formula C5H12. Chlorination of one of these isomers yields only one product. Identify the isomer, and draw the product of chlorination.
(S)-2-Iodopentane undergoes racemization in a solution of sodium iodide in DMSO. Explain.
Draw bond-line structures for all constitutional isomers with molecular formula C4H9Cl.

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