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Elimination reactions remove small molecules from saturated compounds to form alkenes, primarily focusing on alcohol dehydration and haloalkane dehydrohalogenation via E1 or E2 mechanisms. E1 occurs with tertiary alcohols and involves a carbocation intermediate, while E2 occurs with primary or secondary haloalkanes in a single step without intermediates. Zaitsev’s rule indicates that the more substituted alkene is usually the major product, and key exam tips include naming the mechanism and showing curly ar

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aryaganesh

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EN