(Solved): The following is a nucleophilic substitution reaction of \( \mathrm{R}-3 \)-bromohexane with \( \ma ...

The following is a nucleophilic substitution reaction of \( \mathrm{R}-3 \)-bromohexane with \( \mathrm{SH} \). The experimental rate law for this reaction is Rate \( =k \) [R-3-bromohexane] ['SH] The mechanism for this reaction is \( \mathrm{S}_{\mathrm{N}} 2 \) Draw the organic molecule(s) which is(are) formed in this reaction. Do not include molecules like \( \mathrm{H}_{2} \mathrm{O} \) or \( \mathrm{HCl} \). Draw the specific configuration (R or S) at any chiral carbons within your product(s). If both configurations are formed in the product(s), draw both as separate molecules/products: (You have 2 chances until the answer will be given; you have already tried 0 times). Draw only one molecule in each drawing box. If need more compounds for your answer, click this buttòn