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: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter23: Addition To A Carbonyl

Section: Chapter Questions

Problem 25E

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4) This is a "retrosynthesis" problem. Identify the TWO MOLECULES necessary to amine shown below via reductive amination. a NH
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What is the first step in planning a retrosynthesis of the amine shown below. 1st retrosynthesis step? Carbon heteroatom (C-X) disconnection between the carbon-nitrogen bond B Functional group interconversion to an imine C Functional group interconversion to an amide D Reductive elimination
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( -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
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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