Alkanes Flashcards

(49 cards)

1
Q

What types of bonds does carbon form in compounds?

A

Covalent

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2
Q

How many bonds does carbon always form?

A

4 covalent bonds

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3
Q

Molecular formula

A

The number of atoms of each type of element in a molecule

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4
Q

Empirical formula

A

The simplest ratio of atoms of each type of element in a compound

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5
Q

Structural formula

A

This shows the arrangement of atoms in the molecule

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6
Q

Displayed formula

A

This shows all the bonds between the atoms in a molecule

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7
Q

Skeletal formula

A

This shows the shape of the carbon skeleton

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8
Q

Structural isomers

A

Compounds which have the same molecular formula but different structural formula

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9
Q

Functional group

A

A group of atoms responsible for the characteristic reactions of a compound

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10
Q

Alcohol functional group

A

OH

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11
Q

Carboxylic acid functional group

A

COOH

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12
Q

Amine functional group

A

NH2

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13
Q

Alkene functional group

A

C=C

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14
Q

Chloro functional group

A

Cl

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15
Q

Aldehyde functional group

A

CHO

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16
Q

Homologous series

A

A family of compounds containing the same functional group and the same general formula but with each successive member has an extra CH2

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17
Q

Hydrocarbons

A

Compounds containing carbon and hydrogen only

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18
Q

Saturated hydrocarbon

A

Only contains C-C single bonds

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19
Q

Unsaturated hydrocarbon

A

Contains a C-C multiple bond

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20
Q

Aliphatic hydrocarbon

A

Branched, unbranched or non aromatic ring

21
Q

Alicyclic hydrocarbon

A

Non aromatic ring

22
Q

Aromatic hydrocarbon

A

Contains one or more benzene rings

23
Q

The general formula of an aliphatic alkane

24
Q

What is the structure of an aliphatic alkane?

A

They can have branched or unbranched chains

25
What type of hydrocarbon are alkanes?
Saturated
26
What types of bonds are the C-C and C-H bonds in alkanes?
Sigma bonds
27
Sigma bonds
The overlap of orbitals between bonding atoms
28
What is the bond angle and bond shape in alkanes?
109.5 and tetrahedral
29
Why do alkanes not react with most common reagents?
Because they have high bond enthalpies due to strong bonds and they have a low polarity of the sigma bonds due to carbon and hydrogen having similar electronegativities
30
Which alkanes will show structural isomerism?
Those with 4 or more carbons
31
The general formula of a cyclic alkane?
CnH2n
32
What two factors does the boiling points of alkanes depend on?
Chain length and chain branching
33
What is the trend in boiling points with chain length in alkanes?
As the number of carbons increase, the boiling points will increase
34
Explain the trend in boiling points with chain length in alkanes?
As the number of carbons increase there is more points of contact so there are more London forces present so more energy is needed to overcome the forces
35
What is the trend in boiling points with chain branching in alkanes?
Branched chain alkanes have lower boiling points than their unbranched isomers
36
Explain the trend in boiling points with chain branching in alkanes?
As the branching increases there is less points of contact so there is less London forces present so less energy is needed to overcome the forces
37
Complete combustion
In a plentiful supply of oxygen, carbon dioxide and water are produced
38
Incomplete combustion
When insufficient oxygen is present, carbon monoxide and water are produced and can also result in the formation of carbon and water
39
Halogenation
When alkanes react with halogens such as chlorine and bromine
40
What are the conditions of halogenation?
UV light
41
What is the type of mechanism in halogenation?
Radical substitution
42
What is the type of bond breaking in halogenation?
Homolytic fission
43
Homolytic fission
The breaking of a covalent bond to form 2 radicals
44
What are the products of halogenation?
Haloalkane + either HCl or HBr
45
Initiation step of halogenation
Chlorine radicals are produced because UV light has sufficient energy to break the Cl-Cl bond
46
Radicals
Species that contain unpaired electrons
47
Propagation step of halogenation
A radical reacts with a molecule, and a new radical and molecule are produced, leading to a chain reaction
48
Termination step of halogenation
Two radicals combine and the reaction sequence stops
49
What are two limitations of halogenation reactions?
Further substitution and substitution on different carbons