Chemistry- Organic Chemistry Flashcards

(57 cards)

1
Q

organic compounds

A

covalently bonded compounds containing carbon, excluding carbonates and oxides

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2
Q

catenation

A

the covalent bonding of an element to itself to form chains and rings

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3
Q

hydrocarbons

A
  • compounds of only carbon and hydrogen
  • simplest organic compounds
  • often contain O, N, S, and halogens
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4
Q

isomers

A
  • compounds that have the same molecular formula but different structures
  • have different properties due to different arrangement
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5
Q

structural formula

A

indicates the number and types of atoms present in a molecule and the bonding arrangement of the atoms

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6
Q

structural/ constitutional isomer

A

substances that have identical molecular formula but different structural formulas

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7
Q

geometric isomers

A
  • often contain a double bond

- isomers in which the order of atom bonding is the same but the arrangement of atoms in space is different

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8
Q

cis

A

atoms or groups of atoms are on the same side of the double bond

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9
Q

trans

A

atoms or groups of atoms are on opposite sides of the double bond

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10
Q

saturated

A
  • compound containing only carbon-carbon single bonds

- difficult to break down

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11
Q

unsaturated

A

compound containing at least one double or triple carbon-carbon bond

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12
Q

molecular formula

A
  • shows the number of atoms of each element present

- ex. CH4 (methane)

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13
Q

stereochemical formula

A

shows molecule in 3-D

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14
Q

condensed structural formula

A
  • hybrid of molecular and structural formulas

- ex. CH3CH3 (C2H6)

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15
Q

skeletal/ bond line

A

abbreviated way to draw organic compounds

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16
Q

alkanes

A

saturated hydrocarbons with all single bonds

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17
Q

alkenes

A
  • unsaturated hydrocarbon with one carbon-carbon double bond
  • ends with “-ENE”
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18
Q

alkynes

A

unsaturated hydrocarbon with one carbon-carbon triple bond

- ends with “-YNE”

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19
Q

naming alkanes

A
  • count # of carbons in the longest, continuous chain
  • use Table P to find appropriate prefix
  • end with -ANE
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20
Q

functional group

A
  • any atom or group of atoms that is not part of the parent structure
  • primarily responsible for the properties of a molecule
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21
Q

halides

A
  • one or more halogen atoms are substituted for one or more hydrogen atoms
  • fluoro, chloro, iodo, bromo
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22
Q

naming halides

A
  • must have a locator number

- add the correct prefix (of halogen and # of carbon)

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23
Q

naming alcohols

A
  • drop the “e” and add “-OL”

- must have a locator

24
Q

ethers

A

two hydrocarbon groups are bonded to the same oxygen atom

25
naming ethers
- does not need a locator - count the shorter one first and end both with "-yl" - end the name with ether
26
aldehydes
carbonyl group (double bond with oxygen) is attached to a carbon atom at the end
27
naming aldehydes
- name parent chain | - drop the "e" and replace with "-AL"
28
ketones
have a non-terminal carbonyl group
29
naming ketones
- name parent chain (# of carbons) - drop the "e" and use "-ONE" - use locator number
30
organic acids
have a terminal carboxyl (COO) group
31
naming organic acids
- name parent chain - drop "e" and replace with "-OIC ACID" - no locator number necessary
32
esters
contains a carboxyl group that is NOT terminal
33
naming esters
- locate COO - first name part bonded to oxygen (-YL) - then name part double bonded to oxygen (include the carbon bonded to oxygen) and end with "-OATE"
34
amines
contains a nitrogen atom
35
naming amines
- name parent chain - drop "e" and replace with "-AMINE) - use locator
36
amides
contains a terminal carbonyl group bonded to a nitrogen atom
37
naming amides
- name parent chain | - drop "e" and replace with "-AMIDE"
38
naming organic molecule without functional group
- determine prefix by counting carbons | - if it is unsaturated, include location
39
naming "branched" hydrocarbons
- count number of carbons in the longest carbon chain (root of the name) - name the functional group using "-YL" - use locator number - ex. 2-methyl butane
40
alkyl groups
- smaller carbon chains that stick out from the parent chain | - missing one hydrogen atom and ends with "-YL"
41
naming cyclical compounds
- count the carbons in the ring and add prefix "CYCLO-" | - identify the location of the functional group if there is more than one present
42
benzene
- pi electrons (two electrons in each double bond) are delocalized - they are shared between all the carbon atoms in the structure
43
substitution reaction
- one or more atoms replace another in a molecule - between alkane (single bonds) and halogen/ hydrogen - occurs in multiple steps
44
addition reaction
- hydrogen or halogen is added across a double or triple bond - only works with unsaturated hydrocarbons - increases molecule's saturation
45
hydrogenation
- type of additional reaction | - hydrogen is added to an unsaturated molecule
46
condensation/ esterification reaction
- reaction between alcohol and organic acid resulting in the formation of an ester - H from alcohol is taken and OH from organic acid is taken out
47
elimination reaction
- a simple molecule such as water or ammonia is formed from adjacent carbon atoms of a larger molecule - opposite of addition reaction - saturated to unsaturated
48
combustion
- reaction where one of the reactants is oxygen | - often associated with burning
49
complete combustion
- oxygen is in excess | - creates water and carbon dioxide
50
incomplete combustion
- oxygen is limited | - creates water and carbon monoxide
51
fermentation
chemical process in which yeast breaks down sugar into CO2 and ethanol
52
saponification
soap and glycerol is made by reacting fatty acids (fats) with a strong base (NAOH/KOH)
53
polymers
large molecules made of many small units joined to each other through organic reactions
54
monomer
- simple | - small units that make up a polymer
55
copolymer
polymer made from two or more different monomers
56
addition polymers
- formed by addition reactions between monomers that contain a double bond - "n" means that it is repeated indefinitely
57
condensation polymers
- formed by condensation/dehydration reactions - monomers must contain two functional groups - usually copolymers with two monomers in alternating order - must have function groups with -OH