relative rate of SN1 reaction when 40% water plus 60% Ethane out as a solvent
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In our discussion of chemical kinetics we described two alternative reaction profiles that are typical of nucleophilic aliphatic substitution reactions. They are reiterated in Figure 1. The profile in the left-hand panel is typical of nucleophilic aliphatic substitution reactions that proceed by a concerted, 1-step process, i.e. by an Sn2 mechansim. We are now going to look at a group of nucleophilic aliphatic substitution reactions that proceed by a non-concerted, 2-step process.
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