1. Other Organic Compounds

2. Hydrocarbon derivatives are organic molecules that contain one or more elements in addition to carbon and hydrogen.

3. A functional group is an atom or group of atoms in hydrocarbon derivatives that contain elements in addition to carbon and hydrogen.

4. In developing a general formula for types of organic compounds, the symbol R is used.

5. R represents a hydrocarbon fragment. Example: methyl group

6. The symbol R is from the German radikal.

7. A second R group is called R and a third R group is called R .

8. Alcohols

9. Alcohols have the general formula R  OH.

10. In the case of alcohols, the hydroxyl group, OH  1 is a substituent on a hydrocarbon.

11. Alcohols are named by replacing the  e on the end of the parent hydrocarbon with  ol.

12. Numbering may be necessary. The hydroxyl group is to be on the lowest number carbon.

13. Example: CH 3 OH is methanol because the R group comes from methane.

14. ethanol CH 3 CH 2 OH

15. 1-propanol CH 3 CH 2 CH 2 OH

16. 2-propanol CH 3 CHCH 3  OH

17. 6-bromo-2-methyl-2-hexanol CH 3  CH 3 CCH 2 CH 2 CH 2 CH 2 Br  OH

18. Ethers

19. An ether is an organic compound in which two hydrocarbon groups are joined to an oxygen.

20. The general formula for an ether is R  O  R

21. It is named with  oxy  in between the R group names.

22. CH 3 OCH 2 CH 3 is named methoxyethane

23. CH 3 OCH 3 methoxymethane

24. CH 3 CH 2 OCH 2 CH 3 ethoxyethane

25. Ethoxyethane (commonly called diethyl ether) was once the ether most widely used as an anesthetic in surgery.

26. Aldehydes

27. The carbonyl group is  C=O.

28. An aldehyde is an organic compound containing the carbonyl group bonded to at least one hydrogen.

29. The general formula of an aldehyde is O ║ R  C  H

30. Aldehydes are named with the suffix  al instead of the usual hydrocarbon ending.

31. The aldehyde carbon is always assigned as number one for referencing substituent positions in the name. Therefore, numbering is not necessary.

32. The name of the parent chain includes the carbon in the aldehyde.

33. CH 3 CH 2 CHO is propanal.

34. CH 3 CHO ethanal

35. CH 3 CH 2 CH 2 CHO butanal

36. Ketones

37. A ketone is an organic compound containing the carbonyl group.

38. The general formula of a ketone is O ║ R  C  R

39. Ketones are named with the final  e being replaced by  one and a number indicates the position of the carbonyl group where necessary.

40. The name of the parent chain includes the carbon in the ketone.

41. CH 3 COCH 2 CH 3 is called 2-butanone.

42. CH 3 COCH 3 propanone

43. CH 3 COCH 2 CH 2 CH 3 2-pentanone

44. Carboxylic Acids

45. A carboxylic acid is an organic compound containing the carboxyl group.

46. A carboxylic acid has the general formula RCOOH.

47. O ║ R  C  OH

48. Carboxylic acids are named by changing the suffix of the parent hydrocarbon to  oic acid.

49. The carbons are numbered so the carbon in the carboxyl group is the number one carbon.

50. CH 3 COOH is ethanoic acid.

51. CH 3 CH 2 CH 2 CH 2 COOH pentanoic acid

52. CH 3 CH 2 CH 2 COOH butanoic acid

53. Br CH 3   CH 3 CHCHCOOH 3-bromo-2-methylbutanoic acid

54. Esters

55. An ester is an organic compound produced by the reaction between a carboxylic acid and an alcohol.

56. Esters often have a sweet, fruity odor that is in contrast to the often pungent odors of the parent carboxylic acids.

57. An ester has the general formula RCOOR.

58. O ║ R  C  O  R

59. Esters are named by naming the R groups on either side of the COO group.

60. The R group bonded to the oxygen will have a  yl ending and the R group bonded to the C=O will have an  oate ending.

61. The carbon in the carbonyl group is counted with the carbon to which it is attached.

62. CH 3 CH 2 CH 2 OOCCH 3 is propyl ethanoate

63. O ║ CH 3 C  O(CH 2 ) 7 CH 3 octyl ethanoate

64. HCOOCH 3 methyl methanoate

65. CH 3 CH 3   CH 3 CHCH 2 COOCHCH 3 isopropyl 3-methylbutanoate

66. Amines

67. An amine is an organic base derived from ammonia in which one or more of the hydrogen atoms are replaced by organic groups.

68. An amine has the general structure R  NH 2.

69. Amines are named with by changing the parent hydrocarbon’s suffix to  amine.

70. CH 3 CH 2 NH 2 ethanamine

71. Amines can be classified as primary, secondary, or tertiary depending on the number of N  H bonds that have been replaced by N  C bonds.

72. CH 3 NH 2 is a primary amine.

73. (CH 3 ) 2 NH is a secondary amine.

74. (CH 3 ) 3 N is a tertiary amine.

75. Amides

76. An amide is an organic compound whose molecules have any one of the following groups:

77.  CONH 2  CONHR  CONR 2

78. Amides are named by changing the parent hydrocarbon’s suffix to  amide.

79. CH 3 CONH 2 ethanamide

80. CH 3 CH 2 CH 2 CH 2 CONH 2 pentanamide

81. Nitriles

82. Nitriles have the general formula R  C  N.

83. Nitriles are named by adding the word “nitrile” to the parent hydrocarbon.

84. CH 3 CH 2 CH 2 CN butanenitrile

85. CH 3 CH 2 CH 2 CH 2 CN pentanenitrile