Quiz 2 Flashcards

1
Q

Alkanes

A
  • Flammable! Undergoes combustion reactions
  • Nonpolar
  • Melting and boiling points are directly proportional to the strength of intermolecular forces
  • Strength of London dispersion forces between molecules are directly proportional to the surface area of the molecules
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2
Q

Flammable! Undergoes combustion reactions

A

alkane + O2 (excess) = CO2 (g) + H2O (g) + energy

alkane + O2 (difficient) = C (s) + 2 H2O (g)
 CO (g) + 2 H2O (g)

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3
Q

Nonpolar

A
  • Immiscible (i.e. do mix) with water or other polar molecules
  • Very weak London dispersioin forces keep molecules attracted to one another
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4
Q

Strength of London dispersion forces between molecules are directly proportional to the surface area of the molecules

A
  • Boiling points increase substantially with molecular weight
  • Boiling points decrease somewhat with braching; i
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5
Q

propane

A

C3H8, -42 C

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6
Q

butane

A

C4H10, 0 C

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7
Q

2,2-dimethylpropane

A

C5H12, 10 C

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8
Q

2-methylbutane

A

C5H12, 28 C

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9
Q

pentane

A

C5H12, 36 C

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10
Q

hexane

A

C6H14, 68 C

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11
Q

1 – 4

A

gas, heating fuels (natural gas)

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12
Q

5 – 8

A

volatile, gasoline, non-polar solvents

-liquid evaporates quickly at high vapor pressure

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13
Q

9 – 17

A

“stable”, kerosene, diesel, jet fuel

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14
Q

18+

A

“stable”, lubricating oil, asphalt

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15
Q

ALKENES

A

contains a C = C (unsaturated)

vs. alkanes: more reactive, slightly lower BP/MP

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16
Q

ethane

A

30 g/mol

BP = 185 K (-89˚C)

17
Q

ethene (ethylene),

A

28 g/mol

BP = 170 K

18
Q

propane

A

44 g/mol

BP = 231 K

19
Q

propene (propylene),

A

42 g/mol

BP = 226 K

20
Q

butane

A

58 g/mol

BP = 274 K

21
Q

1-butene

A

56 g/mol

BP = 267 K

22
Q

trans-2-butene

A

BP = 274 K

23
Q

cis-2-butene

A

BP = 277 K

24
Q

CIS-TRANS ISOMERS

A

C – C bonds rotate freely

C = C bonds locked into place

25
Q

Cis

A

non-H substituents on the same side

26
Q

trans

A

non-H substituents non-H substituents

27
Q

HYDROGENATION

A

H2 w/ Pt/Pd/Ni catalyst

28
Q

BROMINATION

A

Br2 w/ light catalyst

29
Q

HYDRATION

A

H2O w/ H2SO4 catalyst

30
Q

ADDITION REACTIONS

A

OH attaches to C with most number of substituents

If same on both ends of C = C: two products are formed

31
Q

Aromatic ring

A

: 6-membered ring with alternating C=C & C – C bonds

3 double bonds: actually spread out
delocalized electrons
mostly unreactive C = C

32
Q

Aromatic ring ex

A

benzene

C6H6 (major carcinogen!)

33
Q

ALTERNATIVE SUBSTITUENT LOCATION NOMENCLATURE: for two substituents

A
1,2 = “ortho” (adjacent)
1,3 = “meta”
1,4 = “para”	(opposite
34
Q

benzoic acid

A

food preservative

35
Q

benzaldehyde

A

almond smell

36
Q

phenol

A

old disinfectant (Joe Lister)

37
Q

aniline

A

precursor to polyurethane

rotten fish smell

38
Q

toluene

A

indust. Solv.

rec. inhalant

39
Q

substituents:

A

Different functional groups attached to benzene