11. One doctor allowed 2-methylbutane to undergo chlorination at 300°C and obtained as products 36% 1-chloro-2-methylbutane, 18% 2-chloro-2-methylbutane, 28% 2-chloro-3-methylbutane, and 18% 1-chloro-3-methylbutane. Calculate the relative ease of removal of a hydrogen atom from a tertiary, secondary, and primary carbocation? (8%)

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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11. One doctor allowed 2-methylbutane to undergo chlorination at
300°C and obtained as products 36% 1-chloro-2-methylbutane,
18% 2-chloro-2-methylbutane, 28% 2-chloro-3-methylbutane, and
18% 1-chloro-3-methylbutane. Calculate the relative ease of
removal of a hydrogen atom from a tertiary, secondary, and
primary carbocation? (8%)
Transcribed Image Text:11. One doctor allowed 2-methylbutane to undergo chlorination at 300°C and obtained as products 36% 1-chloro-2-methylbutane, 18% 2-chloro-2-methylbutane, 28% 2-chloro-3-methylbutane, and 18% 1-chloro-3-methylbutane. Calculate the relative ease of removal of a hydrogen atom from a tertiary, secondary, and primary carbocation? (8%)
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