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20.5.1 DEDUCE THE REACTION PATHWAYS GIVEN THE STARTING MATERIAL AND THE PRODUCT. (ONLY TWO CONVERSIONS REQUIRED) 20.5 Reaction Pathways.

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Presentation on theme: "20.5.1 DEDUCE THE REACTION PATHWAYS GIVEN THE STARTING MATERIAL AND THE PRODUCT. (ONLY TWO CONVERSIONS REQUIRED) 20.5 Reaction Pathways."— Presentation transcript:

1 20.5.1 DEDUCE THE REACTION PATHWAYS GIVEN THE STARTING MATERIAL AND THE PRODUCT. (ONLY TWO CONVERSIONS REQUIRED) 20.5 Reaction Pathways

2 Additional Reaction Pathways HL

3 Reaction Pathways You are responsible to be able to convert a reactant into any product listed here, but it can only be through 2 steps. Could be anything, however we’ll focus on the one that is mentioned in the syllabus

4 Conversion of 1-bromopropane to 1-butylamine 1.1-bromopropane can be reacted with potassium cyanide (KCN) to form butanenitrile. 2.Butanenitrile is reduced by heating with hydrogen and a nickel catalyst to form 1- butylamine.

5 Step 1: forming nitrile This example shows the mechanism for bromoethane, but it would be similar for 1-bromopropane.

6 Step 2: forming amide It would be propanenitrile, instead of an unknown chain length and we would heat it with hydrogen and use Ni as a catalyst.

7 Try a couple on your own. You can look at the flow chart and make them up, or try these. Don’t forget to mention conditions for the steps involved. 1.Conversion of 2-butene to 2-butanamine 2.Conversion of propene to butanenitrile


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