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answe plz asap Elimination of HCl from (S)-2-chlorobutane in the presence of a strong base affords only the Z-alkene whereas elimination from (R)-2-chlorobutane affords only
answe plz asap
Elimination of HCl from (S)-2-chlorobutane in the presence of a strong base affords only the Z-alkene whereas elimination from (R)-2-chlorobutane affords only E-alkene as shown below. Propose a mechanism and a full explanation for the observed stereochemical outcome of these reactions. [19 marks] Step by Step Solution
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