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What sequence of reagents should be used to convert the following cyclic alkene into a diol? (List each reagent in the correct order.)

[tex]\[
\begin{array}{c}
\text{cyclic alkene} \\
\downarrow \\
\text{Reagent 1} \\
\downarrow \\
\text{Reagent 2} \\
\downarrow \\
\text{OH + enantiomer} \\
\end{array}
\][/tex]

OH
+
enantiomer

OH


Sagot :

Final answer:

To convert a cyclic alkene into a diol, OsO4 followed by Na₂SO3 (or KMnO4, OH, H2O) is used.


Explanation:

OsO4, 25°C is used first to add hydroxyl groups to the alkene, forming a cyclic diol. Then, Na₂SO3 (or KMnO4, OH, H2O) is used to further oxidize the diol, resulting in the formation of the diol product.


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