4) (2 pts.) This is a "retrosynthesis" problem. Identify the TWO MOLECULES necessary to prepare theamine shown below via reductive amination.CN-CH₂N.CH3

Step 1:Two ways are possible 1) way with one molecule 2) way two molecules Step 2:Answer is 2) way…

Answered: 4) (2 pts.) This is a "retrosynthesis"…

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter23: Amines

Section: Chapter Questions

Problem 23.51P

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Similar questions

Rank the following compounds in order of increasing basicity in aqueous solution, least basic first a) Propylamine, ammonium, dipropylamine b) Methyl-3-aminopropanoate, sectutylamine, NH3*CH2CH2NH2 c) Aniline, methyl m-aminobenzoate,, methy! p-aminobenzoate
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(d) When a primary amine is combined with a ketone, both an imine and an enamine can be obtained. With most ketones, the major product is the imine, as shown: H3C NH2 -N -CH3 -CH3 imine: major product enamine: minor product However, in some cases, like the one shown below, the major product is the enamine. CO₂Et CO₂Et CO₂Et H H3C NH2 -CH3 imine: minor product -CH3 enamine: major product Referring to specific features of the starting materials, intermediates, or products, explain why.
i need the answer quickly
6. Draw the products formed upon Hofmann Elimination of the two isomeric amines below. (Excess CH3-I and K₂CO3 then Ag₂O) of NH₂
( -NH NH Identify the Bronsted base in the following reaction of I and II shown below. НО 11 CF₂ CF₁ A) compound I B) compound II
When 2-methylcyclohexanone is treated with pyrrolidine, two isomeric enamines areformed.Why is enamine A with the less substituted double bond the thermodynamicallyfavored product? (You will find it helpful to examine the models of these twoenamines.)
(1) Which is the most basic amine and which is a secondary amine? (2) Which can undergo hydrolysis? (3) Which gives a diazonium salt upon reaction with HNO2, HCl at 0oC?
4. Propose a synthesis scheme for the amine shown below using the starting material indicated. No mechanisms (electron flow arrows, etc.) are needed! (More than one reaction will be needed to make this amine.) Make: From: NH, and other reagents/reactants
3) (2 pts.) Identify the TWO MOLECULES necessary to prepare the tertiary amine shown below via reductive amination.
Electrostatic potential maps of anisole and thioanisole are shown. Which do you think is the stronger acid, p-methoxybenzoic acid or p-(methylthio)benzoic acid? Explain.
Arrange these compounds in order of increasing acidity: 2,4-dichlorophenol, phenol, cyclohexanol.

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4) (2 pts.) This is a "retrosynthesis" problem. Identify the TWO MOLECULES necessary to prepare the amine shown below via reductive amination. CN-CH₂ N. CH3