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IUPAC Nomenclatrue of Organic Compounds

The document outlines IUPAC nomenclature rules for various organic compounds including alkanes, alkenes, alkynes, alcohols, aldehydes, ketones, carboxylic acids, amines, nitro compounds, halides, dienes, diynes, polyols, diones, nitriles, ethers, and epoxides. A total of 83 examples of organic compounds and their IUPAC names are provided to illustrate the nomenclature system.

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Ryan Samuel
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0% found this document useful (0 votes)
490 views9 pages

IUPAC Nomenclatrue of Organic Compounds

The document outlines IUPAC nomenclature rules for various organic compounds including alkanes, alkenes, alkynes, alcohols, aldehydes, ketones, carboxylic acids, amines, nitro compounds, halides, dienes, diynes, polyols, diones, nitriles, ethers, and epoxides. A total of 83 examples of organic compounds and their IUPAC names are provided to illustrate the nomenclature system.

Uploaded by

Ryan Samuel
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as DOCX, PDF, TXT or read online on Scribd
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IUPAC NOMENCLATURE OF ORGANIC COMPOUNDS

1) CH3 – CH2 – CH – CH3 2-Methylbutane

CH3

2) (CH3)3 – C – CH2 – CH2 – CH – CH3 2,2,5-Trimethyl hexane

CH3

3) CH3 – (CH2)4 – CH – CH3 3-Methyloctane

C2H5

4) CH3 – (CH2)4 – CH – CH2 – CH3 3-Ethyl-2 methyloctane

CH – CH3

CH3

5) CH3 – CH2 – CH = CH2 But-1-ene

6) CH3 – CH = CH – CH3 But-2-ene

7) CH3 – C = CH – CH2 – CH – CH3 2,5-dimethylhex-2-ene

CH3 CH3

CH3

8) CH2 = CH – CH2 – CH2 – C – CH3 5,5-dimethylhex-1-ene

CH3

9) CH3 – CH2 – CH2 – CH2 – CH = CH2 Hex-1-ene

10) CH3 – CH2 – CH2 – CH2 – C ≡ CH Hex-1-yne


CH3

11) CH3 – C – CH2 – C ≡ C – CH3 5,5-dimethylhex-2-yne

CH3

12) CH3 – CH2 – CH – C ≡ C – CH2 – CH3 5-Ethylhept-3-yne

C2H5

13) CH3 – CH2 – OH Ethanol

14) CH3 – CH2 – CH2 – OH Propan-1-ol

15) CH3 – CH2 – CH2 – CH2 – OH Butan-1-ol

16) CH3 – CH – CH2 – CH3 Butan-2-ol

OH

17) CH3 – CH – CH3 Propan-2-ol

OH

18) CH3 – CH2 – CH – CH – CH2 – CH3 4-Methyl hexan-3-ol

OH CH3

19) CH3 – CH2 – CH2 – CHO Butanal

20) CH3 – CH2 – CH2 – CH – CH2 – CH3 2-Ethyl pentanal

CHO
21) (CH3)3 C – CH2 – CH2 – CHO 4,4-Dimethylpentanal

22) CH3 – C– CH3 Propanone

23) CH3 – CH2 – CH2 – CH2 – C – CH3 Hexan-2-one

24) CH3 – CH2 – CH2 – C – CH2 – CH3 Hexan-3-one

CH3

25) CH3 – CH – C – CH2 – C – CH3 4,4,5-Trimethylhexan-2-one

CH3 CH3 O

26) CH3 – CH2 – CH2 – COOH Butanoic acid

27) CH3 – COOH Ethanoic acid

CH3 CH3

28) CH3 – CH – CH – (CH2)3 – CH2 – COOH 6,7-Dimethyloctanoic acid

29) CH3 – CH2 – NH2 Ethanamine

30) CH3 – CH2 – CH2 – NH2 Propan-1-amine


31) CH3 – CH – CH – CH3 3-Methylbutan-2-amine

CH3 NH2

32) CH3 – CH2 – CH2 – CH – CH2 – CH3 2-Ethylpentan-1-amine

CH2 – NH2

32) CH3 – CH2 – CH2 – NH – CH2 – CH3 N-Ethylpropan-1-amine

33) CH3 – CH – CH3 N-Ethylpropan-2-amine

NH – CH2 – CH3

34) CH3 – CH2 – CH2 – NO2 1-Nitropropane

35) CH3 – CH – CH3 2-Nitropropane

NO2

36) CH3 – CH – CH2 – CH – C(CH3)3 2,2,5-Trimethyl-3-nitrohexane

CH3 NO2

37) CH3 – CH2 – Cl Chloroethane

38) CH3 – CH2 – CH2 – Br 1-Bromopropane

39) CH3 – CH – CH3 2-Bromopropane

Br

40) CH3 – CH – CH – CH3 2-Bromo-3-methylbutane

Br CH3
41) CH2 = CH – CH2 – CH = CH – CH3 Hexa-1,4-diene

42) CH2 = CH – CH – CH2 – CH = CH2 3-Methylhexa-1,5-diene

CH3

43) CH3 – CH = CH – CH2 – CH = CH – CH2 – CH = CH2 Nona-1,4,7-triene

44) CH ≡ C – CH2 – C ≡ CH Penta-1,4-diyne

45) CH3 – C ≡ C – CH2 – C ≡ C – CH2 – C ≡ CH Nona-1,4,7-triyne

46) CH2 = CH – CH2 – CH = CH – CH2 – CH = CH2 Octa-1,4,7-triene

47) HO – CH2 – CH2 – OH Ethane-1,2-diol

48) CH3 – CH – CH – CH2 – CH3 Pentane-2,3-diol

OH OH

49) CH2 – CH – CH2 Propane-1,2,3-triol

OH OH OH

50) HO – C – CH2 – CH2 – CH2 – C – OH Pentane dioic acid

O O
51) H – C – CH2 – CH2 – CH2 – CH2 – C – H Hexane dial

O O

52) CH3 – CH2 – C – CH2 – CH2 – C – CH3 Heptane-2,5-dione

O O

53) CH3 – CH2 – CH2 – CH – COOH 2-Hydroxypentanoic acid

OH

54) CH3 – C – CH2 – CH – CH3 2- Methyl-4-oxopentanoic acid

O COOH

55) CH3 – CH2 – C – CHO 2-Oxobutanal

56) CH3 – CH2 – CH – CH2 – C – CH2 – CH3 5-Hydroxyheptan-3-one

OH O

57) BrCH2 – CH2 – CH = CH2 4-Bromobut-1-ene

58) CH3 – CH2 – CH2– CH – CH3 4-Aminopentan-2-ol

OH NH2
59) CH3 – C – CH2 – CH2 – CH2 – NH2 5-Aminopentan-2-one

60) CH3 – CH2 – C – CH – CH2 – CH – CH3 4-Hydroxy-2-methyl-5-oxoheptanenitrile

O OH CN

61) CH3 – CH = CH – CH2 – CH2 – C ≡ CH Hept-5-en-1-yne

62) CH3 – CH = CH – CH2 – C ≡ C – CH3 Hept-2-en-5-yne

63) CH3 – CH = CH – CH2 – CH2 – CH – CH3 Hept-5-en-2-ol

OH

64) CH2 = CH – CH2 – COOH But-3-enoic acid

CH3

65) CH3 – CH = CH – CH2 – CH – CHO 2-Methylhex-4-enal

66) CH3 – O – CH2 – CH2 – CH – CH – COOH 2-Hydroxy-5-methoxy-3-methylpentanoic acid

CH3 OH

67) CH3 – CH – CH2 – CH – CH2 – CHO 3-Hydroxy-5-nitrohexanal

NO2 OH

68) CH3 – CH = CH – CH – CH3 Pent-3-en-2-amine


NH2
69) CH3 – O – CH2 – CH2 – CH – CH3 1,3-Dimethoxybutane

OCH3

70) CH3 – CH2 – CH2 – CH – COOH 2-Formylpentanoic acid

CHO

71) CH3 – C ≡ C – CH2 – C – CH3 Hex-4-yn-2-one

72) CH3 – CH = CH – CH2 – CN Pent-3-enenitrile

73) CH3 – CH – CH2 – CH = CH – CN 5-Methylhex-2-enenitrile

CH3

74) CH3 – CN Ethanenitrile

75) CH3 – CH2 – CN Propanenitrile

76) CH3 – CH2 – CH2 – CH – CH2 – CH3 2-Ethylpentanenitrile


CN

CH3

77) CH3 – C – CH2 – CN 3,3-Dimethylbutanenitrile

CH3

78) CH3 – CH2 – O – CH2 – CH3 Ethoxyethane


79) CH3 – O – CH3 Methoxymethane

80) CH3 – CH2 – O – CH3 Methoxyethane

81) CH3 – CH2 – CH2 – O – CH3 1-Methoxypropane

82) CH3 – CH – CH3 2-Methoxypropane


OCH3

83) CH3 – CH – CH – CH3 2-Methoxy-3-methylbutane


CH3 OCH3

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