GenChem review plus Naming & Structures Flashcards
(69 cards)
0
Q
Eth
A
2 C
1
Q
Meth
A
1 carbon
2
Q
Prop
A
3 C
3
Q
But
A
4 C
4
Q
pent
A
5 C
5
Q
hex
A
6 C
6
Q
hept
A
7 C
7
Q
oct
A
8 C
8
Q
non
A
9 C
9
Q
dec
A
10 C
10
Q
Alkanes only have
A
Carbon and hydrogen atoms (hydrocarbons) single bonds.
11
Q
H replaced by OH=
A
alcohol
12
Q
H repl by NH2=
A
amine
13
Q
H repl by halogen
A
alkyl halide
14
Q
H repl by OR
A
ether
15
Q
Primary
A
attached to 1 other carbon
16
Q
secondary
A
attached to 2 carbons
17
Q
tertiary
A
attached to 3 carbons
18
Q
iso-
A
common name.
Have CH w/ two CH3
19
Q
sec-
A
secondary carbon is attached to the parent chain
attached to 2 other C
20
Q
ter-
A
attached to 3 other carbon
21
Q
Atomic #
A
protons & electrons for a neutral atom
22
Q
mass #
A
P & N
23
Q
Ionic bond
A
metal + nonmetal
24
covalent bond
2 nonmetals
25
most organics are (polarity)
bipolar. Part polar part nonpolar
26
Lewis structure shows
lines, 1 dimensional, + lone pairs, formal charge
27
Kekule structure
similar to Lewis structures w/o lone pairs, formal charge
28
Condensed structures
No bonds shown, all elements involved and how they are bonded. NOT a molecular formula
29
Line bond structure
No C or H shown
30
Lewis acid\*
e- pair acceptors (e- deficient)
31
Lewis base\*
e- pair donors (e- rich)
32
Bronstead-Lowry acid
H+ donor
33
Bronstead-Lowry base
H+ acceptor
34
single bond
σ
35
double bond
σ, π
36
Triple bond
σ, 2π
37
diamagnetic
all e- are paired up
38
paramagnetic
some unpaired e- (anti-bond)
39
Bond order formula
_Bonding electrons – antibonding electrons_
2
40
Formal charge
_(# val e-) - (# lone pair e- )_
2
41
2 groups attached
sp hybridized
## Footnote
sp+sp
42
3 groups attached
sp2
sp2+sp2+sp2
43
4 groups attached
sp3
sp3+sp3+sp3+sp3
44
5 groups attached
sp3d1
45
Conjugate pairs
differ by one H+
acids have more than bases
46
Ka
acid dissociation constant
[products]/ [reactants]
inc Ka inc strength
47
Pka
-log[ka]
↓pka inc acid strength
48
In determining acid/bases ____ predominates over \_\_\_\_\_
size
EN
49
Strongest acids
HCl
HI
H2SO4
HNO3
HClO4
50
weak overlap
H+ easily comes off
51
favorable reactions
strong reactants-\> weaker products(stable)
52
Resonance
Creates a weaker base
53
Formal charge for metals
charge -bonds
54
constitutional isomers
same molecular formula, different drawing (diff connectivity)
55
Parent chain
longest C chain
56
Formal naming
IUPAC names.
Longest parent chain, substituents and location
57
substitients
location-name-loc-name parent
written in alphabetical order (sec,tert don't count)
*#locations=#substituents*
58
Halogens as substituents
fluoro
chloro
iodo
bromo
59
when naming
OH as substituent
Hydroxy
60
ethers
"alkoxy"
ex: OCH3=methoxy
61
isopropyl
Y
62
prefixes (di,tri...) used for
more than one same substituent
63
isobutyl
64
alcohols
alkan-ol
OH=hydroxy (lowest #possible)
65
66
amines
alkan-amine
ex: propanamine
67
Intermolecular forces
dispersion
dipole-dipole
H-bonding
ion-dipole
ion-ion
68