subject
Chemistry, 24.03.2020 18:12 td0715

The Wolff–Kishner reaction uses hydrazine (H2NNH2) and hydroxide (–OH) to reduce a carbonyl to the alkane. The first steps of the mechanism convert a carbonyl to a hydrazone in a manner similar to imine formation. Draw the mechanism arrows for the reaction from the hydrazone to the alkane. Be sure to add lone pairs of electrons and nonzero formal charges to all species.

ansver
Answers: 1

Another question on Chemistry

question
Chemistry, 21.06.2019 18:30
Calculate the change in entropy if br2(l) is converted to br2(g). s° for br2(l) = 152.2 j/(mol•k) s° for br2(g) = 245.5 j/(mol•k) s° for br(g) = 175.0 j/(mol•k)
Answers: 3
question
Chemistry, 22.06.2019 03:00
Which step in naming unsaturated hydrocarbons is used for alkenes but not alkynes
Answers: 2
question
Chemistry, 22.06.2019 23:00
Which of two curves exhibits exponential growth
Answers: 1
question
Chemistry, 23.06.2019 03:00
The size (radius) of an oxygen molecule is about 2.0 ×10−10m. make a rough estimate of the pressure at which the finite volume of the molecules should cause noticeable deviations from ideal-gas behavior at ordinary temperatures (t= 300k ). assume that deviatons would be noticeable when volume of the gas per molecule equals the volume of the molecule itself.
Answers: 3
You know the right answer?
The Wolff–Kishner reaction uses hydrazine (H2NNH2) and hydroxide (–OH) to reduce a carbonyl to the a...
Questions
question
Mathematics, 22.04.2021 21:40