Chapter 3 lecture Flashcards

(84 cards)

1
Q

Heteroatoms

A

Not C or H

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2
Q

Which is the hydrogen bond acceptor and donor and why? (look at word)

A

notes page 75

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3
Q

How can dipole dipole occur?

A

polar molecules where one end is partially positive and the other end is negative

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4
Q

What is the dipole dipole interaction of acetone? (look at word)

A

note page 75

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5
Q

Dipole dipole interaction of CH3-C(triple bond) N

A

note page 75

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6
Q

Van der waal forces

A

Weak interactions caused by momentary changes in electron density and results in temp dipole

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7
Q

What compounds are attractive forces present?

A

nonpolar

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8
Q

What happens for attractive forces between 2 molecules based on surface area

A

Larger surface area= larger attractive force

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9
Q

Which molecule has larger attractive force (on word)

A

note page 75

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10
Q

What does it mean if a compound has a higher temperature boiling point

A

attractive forces are stronger

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11
Q

longer chains cause what

A

Stronger attraction of molecules together

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12
Q

Polizability

A

measure of how electron cloud around atoms respond to changes

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13
Q

What type of atom has stronger VDW forces based on polarizability

A

larger atoms= loosely held= more polarizabile
smaller atoms= tightly held = less polarizablie

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14
Q

Which atom has more polarizability? I or F

A

I is more polarizable

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15
Q

As intermolecular forces increases what also increases

A

Boiling point

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16
Q

Rank increasing boiling points and why? CH3Cl,CH3Br, CH3I, CH3F

A

CH3F,CH3Cl,CH3Br,CH3I

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17
Q

rank highest boiling point and why
1. CH3CH2CH2CH2CH3
2. CH3CH2CH2CH2OH
3. CH3CH2CH2CHO

A

1 VDW
3 DD VDW
2 HB DD VDW

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18
Q

On word doc which has a higher boiling point and why

A

1 because it has more surface area

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19
Q

On word doc rank higher boiling point and why

A

1, 2, 3

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20
Q

What is the increasing strength of intermolecular forces

A

VDW, DD, HB

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21
Q

rank which has highest Melting point and why

A

note page 77

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22
Q

If they all have same F group what will have higher melting point

A

more symmetrical compound

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23
Q

What are the normal solubility trends

A

like dissolves like

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24
Q

organic compound only water-soluble if

A

1 polar functional group that can do hydrogen bonding with solvent for every 5 C atoms

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25
Why do polar solvents dissolve in polar solvents
hydrogen bonding
26
What causes functional groups?
Heteroatoms and Pi bonds
27
What are the parts of an organic molecule?
Hydrocarbon backbone (R), covalent bond, functional group
28
What do functional groups do
determine properties
29
Aliphatic Hydrocarbons
Only made of C and H and have poor reactivity
30
Alkane
R-H
31
Example of Alkane
Note page 55
32
Alkene
R(double bond)FG
33
example of Alkene
Note page 55
34
Alkynes
R(triple Bond)FG
35
Example of Alkynes
Note page 55
36
Phenyl
Note Page 55
37
Aromatic Hydrocarbons
only C and H in a circle with poor reactivity
38
What is the most common Aromatic Hydrocarbon
Beneze
39
Alkyl Halide
R--X (X= F,Cl,Br,I)
40
Example of Alkyl Halide
CH3-I
41
Functional group name of Alkyl Halide
halo
42
Alcohol
R-OH
43
Example of Alcohol
CH3CH2--OH
44
Functional group name of alcohol
hydroxyl
45
How do you know what is the back bone?
larger chain of carbon
46
Ether
R--O--R
47
when is an ether symmetrical and unsymetrical?
Symmetrical when both R are = Unsymmetrical when both R are not =
48
Example of ether
CH3OCH3 CH3OCH2CH3
49
Functional group name of ether
Alkoxyl
50
Amine and names of types
R-NH2 Primary R-NH-R Secondary R-NH-R Tertiary | R
51
Functional Group name Amine
Amino
52
Thiol
R-SH
53
example of Thiol
CH3SH
54
Functional Group name Thiol
Thio mercapto
55
Sulfide (thioether)
R-S-R
56
Example Sulfide (thioether)
CH3-SCH3
57
Functional Group name sulfide (thioether)
Alkylthio
58
Carbonyl Group
C=O
59
Ketone
Note Page 71
60
Example of Ketone
Note page 71
61
Functional group name for Ketone
Carbonyl
62
Aldehyde
Note page 71
63
Example of Aldehyde
Note page 71
64
Functional group name for Aldehyde
Carbonyl
65
Carboxylic acid
Note page 71
66
Example of Carboxylic acid
Note page 71
67
Functional group name of carboxylic acid
carboxyl
68
Ester
Note page 71
69
Example of ester
note page 71
70
Functional group name of ester
ester
71
Amide and types
Note page 71
72
example of amide
note page 71
73
Acid halide
note page 72
74
example of acid halide
note page 72
75
Types of bonds and strengths
Hydrogen bonds strongest, dipole-dipole moderate, van der Waals forces weak
76
Hydrogen bonding
HO, HN, HF attracted to to lone pair on O,N,F
77
Are Hydrocarbons soluble in CCl4 and H2O?
CCl4 yes H2O no
78
Are ketones soluble in CCl4 and H2O?
CCl4 yes H2O yes
79
Why is Aceton solube in CCl4 and H2O
Hydrophobic hydrocarbons= Soluble with CCl4 Hydrophilic O= soluble with H2O
80
Hydrophobic
81
Hydrophilic
82
Which molecules are more soluble in water
83
Vitamin A
84
Vitamin C