Chapter 2 chem ORGANIC CHEMISTRY

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323 Terms

1
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<p>Name</p>

Name

  • 4-ethyl-4,6-dimethyl-5-propylnonane

<ul><li><p>4-ethyl-4,6-dimethyl-5-propylnonane</p></li></ul><p></p>
2
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<p>Name</p>

Name

  • 4-ethyl-2,3,4-trimethylheptane

<ul><li><p>4-ethyl-2,3,4-trimethylheptane</p></li></ul><p></p>
3
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<p>Name</p>

Name

  • 4-ethyl-4-isopropylheptane

<ul><li><p>4-ethyl-4-isopropylheptane</p></li></ul><p></p>
4
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<p>Name</p>

Name

  • 4-ethyl-5-propyloctane

<ul><li><p>4-ethyl-5-propyloctane</p></li></ul><p></p>
5
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<p>Name</p>

Name

  • 1-chloro-3-iodooctane

6
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<p>Name</p>

Name

  • dichlorodifluoromethane

7
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<p>Name</p>

Name

  • 2,4-dibromo-1,6-dichloro-4-iodo-6-methylheptane

8
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<p>Name</p>

Name

  • 4,6-dibromo-1,1,1-trichlorononane

9
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General formula for alkanes?

  • CnH2n+2

10
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General formula for cycloalkanes?

  • CnH2n

11
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<p>name</p>

name

  • methylcyclooctane

12
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  • 1-ethyl-2-methylcyclohexane

13
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<p>name</p>

name

  • 1-ethyl-2-isopropyl-1-methylcyclobutane

14
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<p>Name</p>

Name

  • 1,3-diethyl-5-methylcyclohexane

15
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<p>name</p>

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  • 1-ethyl-2,3-dimethylcyclopropane

16
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17
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<p>name</p>

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18
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<p>name</p>

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19
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Draw:

3-ethyl-5,5-dimethylhept-2-ene

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20
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Draw:

3,4,5-trichloropenta-1,3-diene

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21
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<p>Name</p>

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22
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<p>Name</p>

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<p>Name</p>

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24
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25
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<p>Name</p>

Name

  • 3-chloro-2-methylhexane

26
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<p>Name</p>

Name

  • 2,5-methylhex-1,3,5-triene

27
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draw:

3-isopropylhex-3-ene

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28
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<p>Name:</p>

Name:

  • 3,3-dimethylpent-1-en-5-yne

29
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<p>name</p>

name

  • 4,4-dimethylhex-2-yne

30
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<p>name</p>

name

  • 5-fluoro-6-iodooct-1-yne

31
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<p>name</p>

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  • 2,6-dimethylhept-3-yne

32
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Between a cis geometric isomer and a trans isomer which one has a higher boiling point and why

  • cis does (groups on same side)

  • because cis isomers are polar and have a slight dipole moment that trans isomers do not have

33
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Draw all the constitutional isomers of:

C4H10

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34
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Draw all the constitutional isomers of:

C5H12

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35
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Draw all the constitutional isomers of:

C4H8

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36
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<p>name</p>

name

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37
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<p>name</p>

name

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38
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<p>geometric isomer or not?</p>

geometric isomer or not?

<p></p>
39
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<p>geometric isomer or not</p>

geometric isomer or not

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40
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<p>geometric isomer</p>

geometric isomer

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41
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<p>1) determine whether geometric isometric is possible</p><p>2) name the molecule</p>

1) determine whether geometric isometric is possible

2) name the molecule

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42
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<p>1) determine whether geometric isometric is possible</p><p>2) name the molecule</p>

1) determine whether geometric isometric is possible

2) name the molecule

  • cis-4-chlorohex-2-ene

<ul><li><p>cis-4-chlorohex-2-ene</p></li></ul><p></p>
43
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<p>1) determine whether geometric isometric is possible</p><p>2) name the molecule</p>

1) determine whether geometric isometric is possible

2) name the molecule

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44
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<p>1) determine whether geometric isometric is possible</p><p>2) name the molecule</p>

1) determine whether geometric isometric is possible

2) name the molecule

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45
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<p>1) determine whether geometric isometric is possible</p><p>2) name the molecule</p>

1) determine whether geometric isometric is possible

2) name the molecule

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46
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<p>1) determine whether geometric isometric is possible</p><p>2) name the molecule</p>

1) determine whether geometric isometric is possible

2) name the molecule

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47
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<p>1) determine whether geometric isometric is possible</p><p>2) name the molecule</p>

1) determine whether geometric isometric is possible

2) name the molecule

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48
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<p>1) determine whether geometric isometric is possible</p><p>2) name the molecule</p>

1) determine whether geometric isometric is possible

2) name the molecule

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49
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draw:

cis-1,1,1-trichloro-5-methylhex-3-ene

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50
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Why is the name

cis-4-bromo-2-methylpent-2-ene

incorrect?

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51
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52
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<p>name</p>

name

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<p>name</p>

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<p>name</p>

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<p>name</p>

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59
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<p>name</p>

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<p>name</p>

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<p>draw</p>

draw

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<p>draw</p>

draw

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<p>draw</p>

draw

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<p>draw</p>

draw

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<p>draw</p>

draw

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<p>draw</p>

draw

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67
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<p>draw</p>

draw

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68
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<p>draw</p>

draw

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69
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<p>name</p>

name

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70
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<p>name</p>

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<p>name</p>

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72
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73
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<p>name</p>

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  • toluene

74
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  • aniline

75
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  • phenol

76
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  • benzoic acid

77
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  • o-dibromobenzene

78
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<p>name</p>

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  • m-dibromobenzene

79
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<p>name</p>

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  • p-dichlorobenzene

80
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<p>name</p>

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  • p-bromoiodobenzene

81
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<p>name</p>

name

  • m-chloronitrobenzene

82
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<p>name</p>

name

  • o-methylnitrobenzene

83
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<p>name</p>

name

  • o-methylnitrobenzene

84
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<p>name</p>

name

  • 4-bromophenol

85
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<p>name</p>

name

  • 3-nitrobenzoic acid

86
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<p>name</p>

name

  • 2-iodoaniline

87
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<p>name</p>

name

  • 1,2,4-tribromobenzene

88
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<p>name</p>

name

  • 2-chloro-4-nitrophenol

89
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<p>name</p>

name

  • 2,4,6-trinitrotoluene

90
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Draw:

p-dinitrobenzene

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91
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draw:

m-bromonitrobenzene

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92
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draw:

o-chlorobenzoic acid

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93
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draw:

m-nitrotoluene

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94
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draw:

p-bromoaniline

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95
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draw:

m-iodophenol

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96
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draw:

1,3,5-trimethylbenzene

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97
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draw:

4-chloro-2,3-dinitrotoluene

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98
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draw:

2-amino-5-bromo-3-nitrobenzoic acid

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99
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draw:

2,4,6-trinitrophenol

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100
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<p>1) Examine table 1 on the right. How is the data organized? Is this a useful way to organize data?</p><p>2) You are searching for a trend in boiling points. Reorganize the data to make it more useful</p><p>3) Which substance(s) are gases (have already boiled) at room temperature (22 degrees Celsius)?</p><p>4) Which substance(s) boil between room temperature and body temperature (37 degrees Celsius)</p><p>5) Define<strong> intermolecular forces</strong></p><p>6) What can u infer about the intermolecular forces among decane molecules compared to those in butane?</p>

1) Examine table 1 on the right. How is the data organized? Is this a useful way to organize data?

2) You are searching for a trend in boiling points. Reorganize the data to make it more useful

3) Which substance(s) are gases (have already boiled) at room temperature (22 degrees Celsius)?

4) Which substance(s) boil between room temperature and body temperature (37 degrees Celsius)

5) Define intermolecular forces

6) What can u infer about the intermolecular forces among decane molecules compared to those in butane?

<p></p>