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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14.945798 in us fluid ounce
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there are spaces within the enzymes that is active. That active site allows substrates to join in. This helps the enzyme carry out the chemical reaction with the substrate.
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I don’t see nun tho where’s the objects