ochem Flashcards

(38 cards)

1
Q

Alkanes

A

saturated hydrocarbon
only contains C-H and C-C single bonds
Chemical formula: CnH2n+2

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2
Q

Alkenes

A

unsaturated hydrocarbon
single C-H and double C-C bonds
Chemical formula: CnH2n
* double bonds have priority when counting direction
when double bond is at C #1, don’t put number in the middle of the last thing

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3
Q

Complete structural diagram

A

shows all the atoms in a structure and the way they are bonded to one another

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3
Q

Alkynes

A

unsaturated hydrocarbon
single C-H and triple C-C bonds
Chemical formula: CnH2n-2

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4
Q

Condensed structural diagram

A

Shows the bonds between the carbon atoms but not those between the carbon and hydrogen atoms

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4
Q

Number of C atoms: 2

A

Ethane

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4
Q

Number of C atoms: 1

A

Methane

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5
Q

Line structural diagram

A

shows only lines representing bonds between carbon atoms

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5
Q

Number of C atoms: 4

A

Butane

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6
Q

Number of C atoms: 3

A

Propane

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7
Q

Number of C atoms: 5

A

Pentane

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8
Q

Number of C atoms: 6

A

Hexane

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9
Q

Number of C atoms: 7

A

Heptane

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10
Q

Number of C atoms: 8

A

Octane

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11
Q

Number of C atoms: 9

A

Nonace

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12
Q

Propyl

A

-CH2CH2CH3 for alkyl

12
Q

Number of C atoms: 10

13
Q

Structural Isomers

A

Compounds that have the same molecular formula, but different structures
Example:
- Pentane (C5H12)
- 2-methylbutane (C5H12)

13
Q

Isopropyl

A

CH3-CH-CH3 Where the middle Carbon is attached to another functional group
For alkyl
Also called Propan-2-yl

13
Q

Cycloalkane

A

Carbons are arranged in the form of a ring
Use a line diagram for the cyclic chain
Chemical formula: CnH2n

14
Q

Stereoisomers

A

Geometric Isomers
Pair of molecules differing only in the spatial arrangement of their atoms
Found in some, but not all, alkenes
Occurs due to the RESTRICTED rotation of the C=C bond
This produces two possible structures that are not interchangeable
Groups/atoms are on opposite sides of the double bond = trans-isomers
Groups/atoms are on the same side of the double bond = Cis-isomers

14
Q

Haloalkanes

A

one or more hydrogen atoms have been substituted with halogen atoms (F, C l , Br, I)
1. Name using a prefix (fluoro-, chloro-, bromoor iodo-)
2. List in alphabetical order with alkyl groups and include a position #

15
Q

Benzene

A

C6H6
is composed of six carbon atoms joined in a planar ring with one hydrogen atom attached to each
the bonding structure causes it to be very stable
electrons are shared over the entire molecule
considered 6 identical bonds (halfway between a C–C and C=C)
phenyl- if not parent chain. This is when the other carbon chain has more than 5 carbons.
ortho-ethylmethylbenzene when substituents are on carbon 1 and 2 of benzene
meta-ethylmethylbenzene when substituents are on carbon 1 and 3 of benzene
para-ethylmethylbenzene when substituents are on carbon 1 and 4 of benzene

16
Q

Aromatic Compounds

A

compounds containing a benzene ring

17
Benzenol
Common name: phenol Benzene ring with OH group attached to one C. When more than one OH on Benzene, can;t be phenol For example: OH on Carbon 1 and 2 of Benzene ring is called benzene-1,2-diol
18
Properties of Ethers
Like alkanes, ethers are unreactive substances. Pure ethers cannot form hydrogen bonds and have lower boiling points than similar (carbon length) alcohols. Slightly higher boiling points than hydrocarbon of the same length because the C-O bond is a polar bond
18
Properties of alcohols
Because alcohols have an -OH group, they can form hydrogen bonds with other molecules. This leads to: Higher boiling points and greater solubility than alkanes of the same size Polar -OH group, and non-polar hydrocarbon chain The more hydrocarbons that are attached to one OH, the less soluble it is in water.
19
Thiols
Contain Sulfhydryl group, -SH have a strong odour (ex. skunk, garlic, sewage, additive to natural gas). mainly nonpolar due to the -SH bond (H and S have very similar EN’s). lower melting and boiling points compared to similar length alcohols. Increasing boiling points with more C-H bonds
19
Aldehyde
Contain the carbonyl (C=O) functional group Has the C=O at the end of a parent chain More polar than ketones because of the C-H bonds lower boiling point than alcohol
20
Ketone
Contain the carbonyl (C=O) functional group Has a C=O within the parent chain
21
Carboxylic acid
-oic acid R-COOH When a benzene ring is attached to a carbon that is a carboxylic acid, it's called phenylmethanoic acid (common name: benzoic acid) The polar carboxyl groups cause carboxylic acids to have higher melting points compared to hydrocarbons of similar lengths Since they are polar, carboxylic acids can form hydrogen bonds with water molecules Smaller acids are soluble in water Longer carbon chains in larger acids make them relatively insoluble in water. Carboxylic acids are found in citrus fruits, rhubarb, and other foods with a sour taste.
22
Ester
R-COOR' -oate Esters have a carbonyl group, but no hydroxyl group. This makes them: Less soluble in water than their corresponding carboxylic acids Esters with ≤4 carbons are soluble in water while larger esters are insoluble Have lower boiling points than their corresponding alcohols and carboxylic acids Smaller esters are gases and liquids at room temperature, but the larger esters are waxy solids
22
Amines
an organic compound derived from ammonia (NH3) by replacement of one or more hydrogen atoms with alkyl groups polar compounds that can form hydrogen bonds amines have higher boiling / melting points than similar-sized hydrocarbons amines with low molecular masses have a fishy /decaying odours lower boiling points than similar sized alcohol molecules due to N-H being less polar than O-H
23
Amides
R-CONR' Contain a polar carbonyl group and 1º and 2º amides have at least one –NH group which allows them to form strong hydrogen bonds among themselves Smaller amides are soluble in water because they can form hydrogen bonds with water
24
catalysts
FeCl3, FeBr3, AlCl3
24
toluene
a benzene ring with a hydrocarbon on one of the carbons.
25
UV lights
used when its a cyclohexane with a halogen
26
Acid
Acid like H2SO4 is added to a alkene+water to help make alcohol. can be for hydration and dehydration