GenChem review plus Naming & Structures Flashcards

(69 cards)

0
Q

Eth

A

2 C

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1
Q

Meth

A

1 carbon

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2
Q

Prop

A

3 C

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3
Q

But

A

4 C

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4
Q

pent

A

5 C

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5
Q

hex

A

6 C

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6
Q

hept

A

7 C

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7
Q

oct

A

8 C

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8
Q

non

A

9 C

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9
Q

dec

A

10 C

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10
Q

Alkanes only have

A

Carbon and hydrogen atoms (hydrocarbons) single bonds.

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11
Q

H replaced by OH=

A

alcohol

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12
Q

H repl by NH2=

A

amine

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13
Q

H repl by halogen

A

alkyl halide

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14
Q

H repl by OR

A

ether

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15
Q

Primary

A

attached to 1 other carbon

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16
Q

secondary

A

attached to 2 carbons

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17
Q

tertiary

A

attached to 3 carbons

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18
Q

iso-

A

common name.

Have CH w/ two CH3

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19
Q

sec-

A

secondary carbon is attached to the parent chain

attached to 2 other C

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20
Q

ter-

A

attached to 3 other carbon

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21
Q

Atomic #

A

protons & electrons for a neutral atom

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22
Q

mass #

A

P & N

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23
Q

Ionic bond

A

metal + nonmetal

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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
Heasily 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