Write hydrocarbon radicals that can be formed as intermediates during monochlorination of 2-methylpropane? Which of them is more stable? Give reasons
Write hydrocarbon radicals that can be formed as intermediates during monochlorination of 2-methylpropane? Which of them is more stable? Give reasons
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1 Answer
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This is a short answer type question as classified in NCERT Exemplar
The 2-methylpropane would lead to two types of radicals.
Among the two 3o radical is most stable as it contains 9 ∝ -hydrogen whereas 1o radical contains only 1 ∝ -hydrogen.
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