Organic chemistry

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Organic chemistry by Mind Map: Organic chemistry

1. Reagent: steam

2. Aldehydes

2.1. Reagent: potassium dichromate and dilute sulphuric acid

2.2. Conditions: warm, distillation

2.3. Type of reaction: mild oxidation

2.4. Equation: RCH2OH + [O] --> RCHO + H2O

3. Primary alcohols

4. Alcohols

4.1. Conditions: 300 oC, 60 atm, H3PO4 catalyst

4.2. Type of reaction: electrophilic addition

4.3. CH2=CH2 + H2O -> CH3CH2OH

5. Carboxylic acids

5.1. Reagent: potassium dichromate and dilute sulphuric acid

5.2. Conditions: heat, reflux

5.3. Type of reaction: oxidation

5.4. Equation: CH3CHO + [O] -> CH3COOH

6. Esters

6.1. reaction: esterification

6.2. produces water (condensation)

6.3. conditions: concentrated sulphuric acid

7. Nitriles

8. conditions: RT

9. with inorganic chloride

9.1. CH3CH2OH + SOCL2 ->CH3CH2Cl + SO2 HCl

10. equation: CH3CH=CH2 + Br2 -> CH3CHBrCH2Br

11. reagent: Br2

12. Ketones

12.1. Reagent: potassium dichromate and dilute sulphuric acid

12.2. Conditions: heat, distillation

12.3. Type of reaction: oxidation

12.4. Equation: (CH3)2CH(OH) + [O] --> (CH3)2C=O + H2O

13. Secondary alcohols

14. Polyalkenes

14.1. conditions: low T, high p

14.2. Type of reaction: addition polymerisation (free radical)

15. Dibromoalkanes

15.1. Type of reaction: electrophilic addition

16. Bromoalkanes

16.1. reagent: HBr

16.2. conditions: RT

16.3. Type of reaction: electrophilic addition

16.4. equation: CH2=CHCH3 + HBr -> CH3CHBrCH3

17. Chloroalkanes

17.1. reagents: Cl2

17.2. conditions: UV light

17.3. Type of reaction: free radical substitution

17.4. equation: CH3CH3 + Cl2 --> CH3CH2Cl + HCl

18. Alkanes

19. Alkenes

20. Halogenoalkanes

20.1. Nucleophiles

20.1.1. Water

20.1.1.1. Heat

20.1.1.1.1. CH3CH2OH + HBr

20.1.2. Hydroxide ions

20.1.2.1. Heat with NaOH

20.1.2.1.1. CH3CH2OH + Br ion

20.1.3. Ammonia

20.1.3.1. Heat under pressure in a sealed tube with NH3 in ethanol

20.1.3.1.1. CH3CH2NH2 + HBr

20.1.4. Cyanide ion

20.1.4.1. Heat in ethanol with NaCN

20.1.4.1.1. CH3CH2CN + Br ion

21. Type of bromoalkane

21.1. Primary

21.1.1. SN2

21.2. Secondary

21.2.1. SN1 + SN2

21.3. Tertiary

21.3.1. SN1

22. Tertiary alcohol

23. No reaction

24. Nucleophilic substitution

24.1. with concentrated HBr