1. Explain why 1-bromo-2.2-dimethylpropane has difficulty undergoing both SN2 and SN1 resctions. 2. Can it undergo E2 and E1 reactions? Match the words in the left column to the appropriate blanks in the sentences on the right. Make certain each sentence is complete before submitting your answer. Reset Help 1. The bulky tert-butyl substituent blocks the back side of the bromine to nucleophilic attack, making an secondary E1 bonded to the carbon resction difficult. An Sy1 reaction cannot occur because it would require the formation of an unstable can hydrogen carbocation. cannot 2. It undergo an tertiary reaction, because the B- SN2 carbon is not bonded to a .It undergo an E2 reaction, because that would require the primary formation of a carbocation.

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1. Explain why 1-bromo-2,2-dimethylpropane has difficulty undergoing both SN2 and SN1 reactions.
2. Can it undergo E2 and E1 reactions?
Match the words in the left column to the appropriate blanks in the sentences on the right. Make certain each sentence is complete before submitting your answer.
Reset Help
secondary
1. The bulky tert-butyl substituent blocks the
back side of the
bonded to the
E1
bromine to nucleophilic attack, making an
carbon
reaction difficult. An
Sy1
reaction cannot occur because
it would require the formation of an unstable
can
carbocation.
hydrogen
cannot
2. It
undergo an
tertiary
reaction, because the B-
carbon is not bonded to a
It
SN2
undergo an
E2
reaction, because that would require the
primary
formation of a
carbocation.
Transcribed Image Text:1. Explain why 1-bromo-2,2-dimethylpropane has difficulty undergoing both SN2 and SN1 reactions. 2. Can it undergo E2 and E1 reactions? Match the words in the left column to the appropriate blanks in the sentences on the right. Make certain each sentence is complete before submitting your answer. Reset Help secondary 1. The bulky tert-butyl substituent blocks the back side of the bonded to the E1 bromine to nucleophilic attack, making an carbon reaction difficult. An Sy1 reaction cannot occur because it would require the formation of an unstable can carbocation. hydrogen cannot 2. It undergo an tertiary reaction, because the B- carbon is not bonded to a It SN2 undergo an E2 reaction, because that would require the primary formation of a carbocation.
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