58.7 %
Please correct me if I’m wrong. :)
The tert-butyl chloride in ethanol would surely react faster than the solvolysis of 1-chloro-2,2-dimethyl propane. It is known that both reactions are under the SN2 category so it would be hard for these reactions to occur. However, SN1 reactions are possible because of the ethanol which is a polar solvent. Both would form carbocations but tert-butyl chloride forms a more stable carbocation while the 1-chloro-2,2-dimethyl propane forms a primary carbocation only.
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Any Questions?
So i can give you the answer
I 90% sure that it would be supersaturated
