chem 2 test 1 Flashcards

1
Q

primary alcohol

A

2 H’s

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2
Q

Secoundary Alcohols

A

1 H’s

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3
Q

Tertiary alcohols

A

no H’s

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4
Q

organic compound

A

composed of carbon and hydrogen

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5
Q

Geometric isomers/cis-trans isomers

A

same connectivity but different spatial arrangements

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6
Q

Oxidation reaction (o)

A

single bound OH to double bonded O

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7
Q

dehydration reaction (H+/triangle) or (H2SO4/heat)

A

alcohol (OH) to alkenes (Double bonded)

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8
Q

Alkanes

A

single bonded molecules

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9
Q

molecular geometry of alkanes

A

tetrahedral 109.5

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10
Q

isobutyl

A

chain of three with a methyl on two

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11
Q

secbutyl

A

chain of four, connected on two

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12
Q

tert-butyl

A

cross/X

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13
Q

boiling/melting point for alkanes

A

as number of carbons increase, boiling point increases

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14
Q

boiling/melting point for branching alkanes

A

as the number of branches increase boiling point decreases

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15
Q

combustion of alkanes

A

alkane +O2 = Co2+h20

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16
Q

alkenes

A

double bond

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17
Q

alkynes

A

triple bond

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18
Q

Hydrogenation (H2/Pt,Ni, or Pd)

A

Alkene to alkane (double to single) or alkyne (+2H2) to alkane (triple to single)

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19
Q

hydration (+h-oh -> h2SO4) or (+h20 -> H)

A

alkene to alcohol

20
Q

toluene

A

benzene with methyl

21
Q

aniline

A

benzene with NH2

22
Q

phenol

A

benzene with OH

23
Q

ortho/o

A

common naming for two apart on benzene

24
Q

meta/m

A

common naming for 3 apart on benzene

25
Para/p
common naming for 4 apart on benzene
26
alcohol with 2 OH groups
diol
27
Thiols
SH group
28
ethers
C-O-C
29
alcohols vs ethers boiling point
alcohols have greater boiling point
30
major product
less amount of H on double bond
31
formaldehyde
OH-CH3
32
Aldehyde
o=c to one H and one C
33
Ketone
0=c bonded to two C
34
acetaldehyde (ethanal)
0=c bonded to CH3 and H
35
Tollen's test (aldehyde + 2Ag ->o)
H becomes OH
36
Benedict's test (aldehyde+ 2Cu->)
H becomes OH
37
reduction of Ketones and aldehydes (->pd, pt, or pd)
double bond O breaks to become OH and another H is added
38
Hemiacetals
HO-C-C
39
Acetals
C-O-C-C
40
Aldose
contain h-c=O group on end of carbon backbone
41
Ketose
contains c=0 on side of carbon backbone
42
chiral molecules
same molecular formula but differnt bonding aragements
43
stereoisomers
identical molecular formula bot arranged differently in space
44
chiral
nonsuperimposable mirror images
45
achiral
superimposable
46
L-Isomer
OH on left
47
D-Isomer
OH on right