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In the synthesis of alkyl chloride, comment on the ease of formation of tert-chlorobutane form tert-butanol and concentrated HCl. Why did we not use concentrated HCl when we prepared 1- bromobutane from 1-butanol? You generated the nucleophile from sodium bromide and sulfuric acid, when you prepared 1-bromobutane from 1-butanol. What was the nucleophile generated? What are the other products that can be formed in the presence of sulfuric acid?

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