Chapter 4 book Flashcards

(56 cards)

1
Q

Acyclic alkanes

A

CnH2n+2 and are linear or branched and sp3 and tetrahedral

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

cycloalkanes

A

contains C on rings CnHn

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

Constitutional isomers

A

differ how atoms are connected

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

Methylene group

A

CH2

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

Homologous series

A

Compounds differ by 1 CH2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Systematic naming

A

rules of nomenclature and compounds by chemical structure using IUPAC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Generic naming

A

Official and internationally approved name of drug

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

trade naming

A

name assigned by company that manufacters it

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

Parent name

A

of longest carbon chain

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

suffix

A

indicates functional group

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

prefix

A

indicates identity, location, and # of substituents

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

How to name alkanes

A

Prefix+Parent+Suffix

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

Alkyl groups

A

remove 1 H from alkane

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

Propyl

A

parent-CH2CH2CH3

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

isopropyl

A

parent-CH(CH3)2

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

butyl

A

parent-CH2CH2CH2CH3

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

sec-butyl

A

CH3CHCH2CH#
. |
. Parent

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

isobutyl

A

CH2CH(CH3)2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

tert-butyl

A

C(CH3)3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Naming cycloalkane

A

prefix+cyclo+parent+suffix

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Are alkane polar or nonpolar

A

nonpolar

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

What type of forces do they have

A

Van Der Waals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Explain alkane boiling and melting points

A

normally low
# of C increase=increase surface area=increase BP and MP
If branched=decreases surface area=decrease BP
If branched=increase symmetry=increase MP

24
Q

What are alkanes soluble in

A

organic solvents

25
stereochemistry
3-D structure
26
Conformations
different arrangements of atoms interconverted by rotation around single bond
27
eclipsed conformations
C-H bonds on 1 C aligned with C-H on adjacent C
28
staggered conformations
C-H bonds on 1 C bisect H-C-H bond on other C
29
How do you change an eclipse into a staggered
rotate 60 degrees
30
dihedral angle
angle separates bond on 1 atom from bond on adjacent atom
31
Newman project
shows 3 groups bonded to each C-C with dihedral angles
32
Is staggered or eclipsed more stable
staggered
33
torsional energy
difference between staggered and eclipsed
34
torsional strain
increase in energy caused by eclipsed interactions
35
Which conformation has greater energy for a CH3CH3
eclipsed
36
anti conformation
2 larger groups 180 degres from each other in staggered
37
gauche conformation
2 larger groups 60 degrees from each other in staggered
38
steric strain
increase energy resulting when atoms forced too close to each other
39
Angle strain
increase energy when tetrahedral bond angle is not 109.5
40
baeyer stain theory
rings with bond angles different from tetrahedral bond angle
41
what does chair form do
eliminates angle and torsional strain
42
axial substituent
above and below ring
43
equatorial substituent
in-plane of ring
44
When there are 2 large substituents what conformation is most stable
conformation with both substituents equatorial
45
stereoisomers
differ in how molecules are oriented
46
Cis
2 groups on same side
47
Trans
2 groups on opposite side
48
When is a 1,4-dimethylcyclohexane trans and cis
trans when both substituents are either axial or equatioral cis when one is axial and one is equatioral
49
What reaction occurs with alkanes
Redox
50
When is a compound reduced
C-H increases C-Z decreases and gain of e-
51
when is a compound oxidized
C-H decreased C-Z increased and loss of e-
52
Combustion
a compound burns in presence of O to make CO2 and H2O
53
lipids
biomolecules with properties of alkanes and hydrocarbons
54
What type of solvent are lipids soluble in
inorganic solvents
55
waxes
2 long C chains joined by O
56
prostaglandins
C-C, C-H, and COOH group