Chapter 18: Problem 61
Suppose that you start with a diisocyanate and a diol. Show how their reaction can lead to a polymer called a polyurethane (Section 29.5D).
Chapter 18: Problem 61
Suppose that you start with a diisocyanate and a diol. Show how their reaction can lead to a polymer called a polyurethane (Section 29.5D).
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Get started for freeFollowing is a retrosynthetic analysis for the synthesis of the herbicide (S)-Metolachlor from 2-ethyl-6-methylaniline, chloroacetic acid, acetone, and methanol. Show reagents and experimental conditions for the synthesis of Metolachlor from these four organic starting materials. Your synthesis will most likely give a racemic mixture. The chiral catalyst used by Novartis for reduction in Step 2 gives \(80 \%\) enantiomeric excess of the \(S\) enantiomer.
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Using your roadmaps as a guide, show how to convert 1-bromopentane and sodium cyanide into \(N\)-hexylhexanamide. You must use 1-bromopentane and sodium cyanide as the source of all carbon atoms in the target molecule. Show all reagents and all molecules synthesized along the way.
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