Mechanisms : conditions and reagents

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Last updated 4:26 AM on 10/8/26
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28 Terms

1
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Alkane to alkene

Catalytic cracking

catalyst ; Al2O3

450 degrees

2
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Alkene to alkane

Hydrogenation :

Reagent - H2

Conditions;

- Nickle catalyst

150 degrees

5 atm

3
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Alkane to halogenoalkane

Free radical substitution

- HX/ X2

UV light

4
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Alkene to haloalkane

Electrophillic addition

- HX / X2

5
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Haloakane to alkene

Elimination

- KOH in ethanol

Reflux

6
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Alkene to alcohol

Hydration

- Steam

- Conc H2SO4

- 300 degrees celcius

- 60atm

7
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Alcohol to Alkene

Dehydration

- Excess conc H2SO4

- 170 degrees celcius

8
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Haloalkane to Alcohol

Nucleophilic substituion

- KOH in aq

- reflux

9
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Alcohol to Haloalkane (Chlorine )

Nucleophilic substitution

- Reagent ; PCL5

- Room temp

- HCl gas produced

10
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Alcohol to Haloalkane (Br)

Nucleophilic substitution

- Reagents : KBr and 50% conc H2SO4

- Heat under reflux

11
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Alcohol to Haloalkane (I)

Nucleophilic substitution

- Red phosphorus and Iodine

- Heat under reflux

12
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Primary alcohol to aldehyde

K2Cr2O7/H2SO4, distil

13
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aldehyde to carboxylic acid

K2Cr2O7, H2SO4, reflux

14
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secondary alcohol to ketone

K2Cr2O7, H2SO4, reflux in ethanol

15
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aldehyde to primary alcohol

Reduction

- LiAlH4 in dry ether

- followed by dilute acid

16
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ketone to secondary alcohol

LiAlH4 in dry ether

17
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Ketones/Aldehyde to hydroxynitrile

Nucleophillic addition

- HCN

- Room temp

18
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Nitrile to carboxylic acid (Acidic)

Hydrolysis

- Dilute HCl or H2SO4

- Heat under water

- Will produce Carboxylic acid + Ammonium

19
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Nitrile to Carboxylic acid (alkaline)

Hydrolysis

- Dilute NaOh

- Under reflux

- Dilute HCl or H2SO4

- Will produce a carboxylate salt and ammonia

20
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Carboxylic acid to primary alcohol

reduction, LiAlH4 in dry ether

21
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carboxylic acid to carboxylate salt

Neutralisation

NaOH(aq)

22
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carboxylic acid to acyl chloride

halogenation

PCl5, rtp(anhydrous)

23
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carboxylic acid to ester

Esterification

Alcohol

conc. H2SO4

24
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Acyl chloride to carboxylic acid

Cold H2O

25
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Acyl chloride to ester

alcohol - ethanol

26
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Acyl chloride to primary amide

NH3

27
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Acyl Chloride to N-Substituted Amide

Primary or secondary amine

28
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Diols to polyester

-Condesnation polymerisation

- Add dicarboxylic acid

- Catalyst : H2SO4

Heat under reflux