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Considering the following alkene: The correct decreasing order of stability is: `{:(underset("(I)")underset("But-l-ene")(CH_(3)CH_(2)=CH_(2))", "underset("(II)")underset("2,3-Dimethylbut-2-ene")((CH_(3))_(2)C=C(CH_(3))_(2)",")),(underset("(III)")underset("2-Methylbut-2-ene")((CH_(3))_(2)C=CHCH_(3))", "underset("(IV)")underset("2-Methylpropene")((CH_(3))_(2)C=CH_(2))):}`A. I gt II gt III gt IVB. II gt III gt IV gt IC. IV gt III gt II gt ID. III gt IV gt I gt II

Answer» Hint - More substituted alkene has the greater number of hypercojugative `C-H `bonds and so greater is the stability of alkenes.


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