4.1 Basic Concepts and Hydrocarbons Flashcards

(39 cards)

1
Q

What are aliphatic hydrocarbons?

A

In which the carbon atoms are joined together in straight unbranched chains or branched chains.

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2
Q

What are alicyclic hydrocarbons?

A

Carbon atoms joined together in ring structure.

Not aromatic

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3
Q

What are aromatic hydrocarbons?

A

At least one benzene ring in the structure.

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4
Q

What is nomenclature.

A

Naming system for compounds.

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5
Q

What are alkanes?

A

A homologous series of saturated hydrocarbons

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6
Q

What happens when you remove a hydrogen atom from an alkane?

A

And alkyl group is formed.

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7
Q

General formula for alkanes?

A

CnH2n+2

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8
Q

What is the general formula for alkenes?

A

CnH2n

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9
Q

What is the formula for alcohols?

A

CnH2n+1OH

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10
Q

What’s an isomer?

A

Same molecular formula but different arrangements of atoms.

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11
Q

What are stereoisomers?

A

Organic compounds with the same molecular formula but different arrangements of atoms in space.

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12
Q

Define reaction mechanism

A

Models that show the movement of electron pairs during a reaction.

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13
Q

What are curly arrows for?

A

Model the flow of electron pairs during reaction mechanism

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14
Q

What is homolytic fission?

A

When each bonding atom receives one electron from the bonded pair, forming two radicals.
Fission = bond breaking
Bonded our split EQUALLY

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15
Q

What are radicals?

A

A species with one or more unpaired electrons

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16
Q

What is heterolytic fission?

A

When one bonding atom receives both electrons from the bonding pair

17
Q

What happens to the boiling point of an alkane as chain length increases?

A

Boiling point increases due to larger molecular mass, larger surface area and larger dipole dipole forces.

18
Q

What happens to the boiling point of alkanes as branching increases?

A

Lower boiling points due to fewer surface area interactions, fewer induced dipole dipole

19
Q

Define complete combustion

A

Oxidising a fuel in a plentiful supply of air

20
Q

Define incomplete combustion

A

Oxidising a fuel in a limited supply of air

21
Q

What are alkenes?

A

A homologous series of unsaturated hydrocarbons.

22
Q

What is an electrophile?

A

An electron pair acceptor

23
Q

What is needed for hydrogenation?

A

A temperature of 150 and a suitable catalyst.

24
Q

What can halogenation be used for?

A

A test for saturation.

25
What does the process of hydration require?
High temperatures and high pressures with a phosphoric acid catalyst
26
What is a reaction mechanism?
A model that shows the movement of electrons in an organic reaction.
27
What happens with a hydrogen halide is added to an unsymmetrical alkene?
There are two possible products.
28
What does markownikoffs rule state?
When H-X is added to an unsymmetrical alkene, the hydrogen becomes attached to the carbon with the most hydrogen atoms to start with.
29
Method one monitoring hydrolysis of haloalkanes
AgNO3 Water bath and ethanol 40-80C Relative rate of precipitation
30
Method two monitoring hydrolysis haloalkanes
AgNO3 NaOH NEUTRALISE WITH HNO3 Relative amount of precipitation
31
Uses for CFCs other than propellants
Fire extinguishers decreasing agents Dry cleaning Blowing polystyrene
32
Why are branched alkanes better for fuel?
More efficient combustion
33
How can environmental damage be reduced when dealing with polymers?
``` Making bio or photodegradable polymers Develop ways of sorting AND recycling Use as chemical feedstock by cracking Make from plant based chemicals Use a higher atom economy ```
34
Define homologous series
A series of compounds with the same functional group and each successive member differing by -CH2
35
What metals are in a catalytic converter?
Platinum, rhodium and palladium are thinly spread over a mesh
36
What happens in catalytic converters
Gasses pass over the catalyst
37
Reactions in catalytic converter?
2CO + O2 = 2CO2 | 2NO + 2CO = CO2 + N2
38
What type of forces there there between alkane chains?
London force
39
Why are alkanes not reactive to electrophiles and nucleophiles?
Carbon and hydrogen have similar electronegativities and sigma bonds are hard to break