Ph Ph- CH3 Ph CH3 The Wolff-Kishner reaction involves the reaction of an aldehyde/ketone with hydrazine in the presence of KOH. The process is useful for converting an aldehyde or ketone into an alkane. The reaction involves formation of a hydrazone, followed by base-catalyzed double-bond migration, loss of N₂ gas to give a carbanion, and protonation to give the alkane. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions XE -CH₂CH₂CH3 HỘ NH, H H-OH H₂NNH₂ KOH :OH Ph- :OH -CH₂CH₂CH3 + N₂ + H₂O HẠNH, OH H₂O
Ph Ph- CH3 Ph CH3 The Wolff-Kishner reaction involves the reaction of an aldehyde/ketone with hydrazine in the presence of KOH. The process is useful for converting an aldehyde or ketone into an alkane. The reaction involves formation of a hydrazone, followed by base-catalyzed double-bond migration, loss of N₂ gas to give a carbanion, and protonation to give the alkane. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions XE -CH₂CH₂CH3 HỘ NH, H H-OH H₂NNH₂ KOH :OH Ph- :OH -CH₂CH₂CH3 + N₂ + H₂O HẠNH, OH H₂O
Chapter4: Organic Compounds: Cycloalkanes And Their Stereochemistry
Section4.SE: Something Extra
Problem 62AP: Alcohols undergo an oxidation reaction to yield carbonyl compounds on treatment with CrO3. For...
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