QCAA CHEMISTRY - Reaction Pathways

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22 Terms

1
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Alkane to haloalkane

Through a substitution reaction with the halogen under UV conditions

2
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Alkene to alkane

Through an addition/reduction reaction with hydrogen and a catalyst

3
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Alkene to haloalkane

Through an addition reaction with a hydrogen and halogen (e.g., HCL)

4
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Alkene to dihaloalkane

Through an addition with a dihalogen molecule (e.g., Cl2)

5
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Alkene to Alcohol

Through an addition reaction with heat, H2O and a catalyst

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Alkene to Polymer

Through an addition reaction with a catalyst, heat and pressure

7
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Haloalkane to Alcohol

Through a substitution reaction with reflux and NaOH(aq)

8
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Haloalkane to Amine

Through a substitution reaction with NH3 and conc

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Haloalkane to Nitrile

Through a substitution reaction with KCN and reflux

10
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Haloalkane to Alkene

Through an elimination reaction with NaOH and reflux

11
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Primary Alcohol to Aldehyde

Through an oxidation reaction with H/MnO4 and heat

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Primary Alcohol to Carboxylic Acid

Through a second oxidation reaction (alcohol to aldehyde to carboxylic acid) with H/Cr2O7 and heat for longer

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Secondary Alcohol to Ketone

Through an oxidation reaction with H/MnO4 or H/Cr2O7

14
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Carboxylic Acid to Ester

Through a condensation or esterification reaction with an alcohol and heat

15
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Carboxylic Acid to Salt

Through a neutralisation reaction with a base

16
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Amine to Amide

A condensation reaction with a carboxylic acid

17
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Amine to Salt

A neutralisation reaction with an acid

18
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Nitrile to Amine

A reduction/addition reaction with a H2/Ni catalyst and heat

19
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How are alkanes distinguished from alkenes?

When using Br2, alkenes turn the red colourless

20
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How do you determine the level of alcohols?

Through the number/products of oxidation. Primary alcohols oxidise twice, secondary once and tertiary null.

21
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How to determine between an aldehyde and ketone?

Because aldehydes oxidise and ketones don't, aldehydes turn orange dichromate green and purple manganate pale pink

22
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Markovnikov's Rule

When an unsymmetrical reagent is added to an unsymmetrical alkene, the H goes to the C's that has the most H's