Chemistry, 17.12.2019 04:31, coolquezzie
The reaction of 2,2-dimethyl-1-piopanol with hbr is very slow and gives 2-bromo- 2-methyibutane as the major product. give a mechanistic explanation for these observations. select all that apply. stereoelectronic effects result in an antic op lanar rearrangement of the carbon skeleton. steric hindrance prevents nucleophilic attack. the mechanism requites the development of an unstable positively charged species in the transition state. the mechanism results in a carbocation rearrangement in which a methyl shift occurs. the mechanism requires dissociation of a poor leaving group.
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The reaction of 2,2-dimethyl-1-piopanol with hbr is very slow and gives 2-bromo- 2-methyibutane as t...
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