Hydrolysis Of 2 Bromo 2 Methylpropane Tert Butyl Bromide Yields 2 Methylpropan 2 Ol Ch Cbr 2h O Ch Coh H O Br Be 1 (19.7 KiB) Viewed 70 times
Hydrolysis Of 2 Bromo 2 Methylpropane Tert Butyl Bromide Yields 2 Methylpropan 2 Ol Ch Cbr 2h O Ch Coh H O Br Be 2 (26.73 KiB) Viewed 70 times
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (CH₂),CBr +2H₂O(CH),COH+H,O+Br Be sure to scroll down to see the complete question. A. The reaction proceeds by an S1 mechanism. Identify the steps of the mechanisms. Not all steps will be used. water adds to the alkylbromide water eliminates a p-hydrogen Start of mechanism addition of water to the carbocation End of mechanism AntwerBank deprotonation of protonated water loss of brumine leaving group to form a carbocation addition of bromine to the carbocation
water adds to the alkyl bromide water eliminates a B-hydrogen addition of water to the carbocation Answer Bank deprotonation of protonated water addition of bromine to the carbocation loss of bromine leaving group to form a carbocation B. What is the purpose of the second equivalent of water? The water acts as mechanism. in step of the
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