chapter 2 Flashcards

0
Q

aliphatic hydrocarbon

A
  • fats

- three groups: alkanes, alkenes, alkynes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
1
Q

hydrocarbon

A

organic compound consisting of only hydrogen and carbon

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

alkanes

A

hydrocarbons in which all bonds are single

ex. ethane (C2H6)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

alkenes

A

contain at least one carbon-carbon double bond

ex. ethylene (C2H4)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

alkynes

A

contain at least one carbon-carbon triple bond

ex. acetylene (C2H2)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

aromatic hydrocarbon

A
  • oils
  • arenes
    ex. benzene (C6H6) - ring
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

sigma bond

A
  • a bond in which orbitals overlap along a line connecting the atoms (the inter-nuclear axis)
  • electron distribution is cylindrically symmetrical
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

bonding theory

A
  • starting with 2 atomic orbitals, you end up with 2 molecular orbitals
    • one orbital will be higher in energy
    • one orbital will be lower in energy
      • net result 0
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

molecular orbitals vs atomic orbitals

A

the # of MOs is the same # of AOs that combine to produce them

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

general formula of alkanes

A

CnH2n+2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

methane

A
  • CH4
  • most abundant
  • lowest boiling point
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

ethane

A

-C2H6

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

propane

A

-C3H8

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

methyl group

A

CH3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

methylene group

A

CH2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

constitutional isomers

A

same molecular formula different connectivity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

pentane

A

5 carbons

CH3CH2CH2CH2CH3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

hexane

18
Q

unbranched alkanes

A

straight-chained alkanes (zigzag line)

19
Q

C5H12 isomers

A
  • unbranched isomer = pentane
  • isomer with single methyl group = isopentane
  • isomer with 3C chain and two methyl groups = neopentane
20
Q

methane

21
Q

ethane

22
Q

propane

23
Q

butane

24
pentane
5 carbons
25
hexane
6 carbons
26
heptane
7 carbons
27
octane
8 carbons
28
nonane
9 carbons
29
decane
10 carbons
30
ethyl group
CH3CH2
31
heptyl group
CH3(CH2)5CH2
32
octadecyl group
CH3(CH2)16CH2
33
primary carbon
directly attached to one other carbon
34
secondary carbon
directly attached to two other carbons
35
tertiary carbon
directly attached to 3 other carbons
36
propyl group
CH3CH2CH2 | -common name n-propyl
37
1-methylethyl group
(CH3)2CH | -common name-isopropyl
38
butyl group
CH3CH2CH2CH2 | -common name n-butyl
39
1-methylpropyl
CH3CH2C-(CH3)H | -common name sec-butyl
40
higher boiling point
more carbons in compound
41
lower boiling point
more branched the compound is
42
combustion of alkanes
- higher energy compounds have less branching - more branching, more stable (low energy) - less branching, more unstable (high energy)
43
Cycloalkane
Alkanes that contain a ring of three or more carbons | -CnH2n