Organic Chemistry Flashcards

1
Q

How many bonds can carbon atoms form and why?

A

It can only form 4 bonds because it has 4 electrons in its outer shell

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2
Q

What is a hydrocarbon?

A

A compound made up of only hydrogen and carbon

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3
Q

In what ways are a structural formula and a molecular formula different?

A

A structural formula shows atoms and bonds while a molecular formula shows just atoms

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4
Q

Alkanes are ______ hydrocarbons

A

Saturated

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5
Q

Alkenes are ______ hydrocarbons

A

Unsaturated

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6
Q

What are saturated hydrocarbons?

A

Hydrocarbons with only single bonds between C atoms (alkanes)

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7
Q

What are unsaturated hydrocarbons?

A

Hydrocarbons with a C=C double bond (alkenes)

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8
Q

What are the general formulae for alkanes and alkenes?

A

Akanes: Cn H2n+2

Alkenes: Cn H2n

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9
Q

How is crude oil formed?

A

From remains of marine organisms over millions of years

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10
Q

How are individual hydrocarbons extracted from crude oil?

A

Fractional distillation

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11
Q

What is the first step in fractional distillation?

A

Evaporation of crude oil

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12
Q

Why do fractions condense at different points in a fractional distillation column?

A

Because they have different boiling points. Fractions with a high bp will condense lower in the column (longer chains of C) and fractions with a low bp will condense higher in the column (shorter chains of C)

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13
Q

What happens to the properties of the gases as you rise through a fractional distillation column?

A

Burn easier - better fuels
Chain length decreases
Bpt decreases
Lighter colour

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14
Q

What properties do larger molecules have? (FD)

A

High boiling point
Not very volatile
Do not flow easily
Do not ignite easily

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15
Q

What properties do smaller molecules have? (FD)

A

Low boiling point
Very volatile
Flow easily
Ignite easily

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16
Q

What does volatility mean?

A

How readily a substance vapourises (goes from a liquid to a gas)

17
Q

Which length chains are the most commercially valuable?

A

Short chains because they are the best fuels

18
Q

How can you solve the problem of oversupply of long chain saturated hydrocarbons after fractional distillation?

A

Cracking

19
Q

What is cracking?

A

The breaking down of long chain saturated hydrocarbons (alkanes) using heat and a catalyst

20
Q

What does cracking produce?

A

Shorter chain alkanes (better fuels) and alkanes which can be used to make plastics

21
Q

What will a combustion reaction with an alkane/alkene always produce?

A

Carbon dioxide and water

22
Q

What does hydrogen produce when it burns?

A

Water

2H2+O2->2H2O

23
Q

What can hydrogen be used for?

A

As rocket fuel and increasingly to power cars

24
Q

What are the advantages of using hydrogen as a fuel?

A

It’s renewable because it’s produced from water

Water is the only product made when it burns so it doesn’t contribute to global warming

There’s lots of it about because there’s a lot of water in the environment

25
Q

What are the disadvantages of using hydrogen as a fuel?

A

Large amounts of electricity are needed to produce hydrogen by electrolysis

Storage of fuel in the car is in heavy, pressurised containers

Forms an explosive mixture with air

26
Q

Why is using hydrogen as a fuel not completely carbon-neutral?

A

It takes a lot of electricity to carry out electrolysis to separate hydrogen from water

27
Q

How could we make hydrogen a carbon neutral fuel?

A

Generate energy for electrolysis through renewable sources e.g. wind or solar

28
Q

What is the fire triangle?

A

The 3 things needed to start and maintain a fire

29
Q

How can we apply the fire triangle to fire fighting methods?

A

Removing one of the 3 essential things that keep a fire burning
e.g. Add water -> Removes heat
Fire blanket -> Removes oxygen
Create fire break -> Removes fuel

30
Q

What are isomers?

A

Molecules with the same molecular formula but a different structural formula

31
Q

How do we name isomers?

A

Based on how many carbon atoms can be in a line

e.g. Butane has the same number of carbon atoms as methylpropane

32
Q

In what case do we use the preposition methyl-?

A

When there is one side-chain of carbon stemming from the longest chain

e.g. Methylpropane
(isomer of butane)

33
Q

In what case do we use the preposition dimethyl-?

A

When there are two side-chains of carbon in opposite directions from the longest possible chain

34
Q

In what case do we use the preposition ethyl-?

A

When there is a side chain consisting of two carbon atoms stemming from the largest possible line of carbon atoms

35
Q

How can you create a different isomer in an alkene without creating a side-chain?

A

By moving the position of the double bond

We show this by placing a number in the middle of the name
e.g. But-1-ene or But-2-ene

36
Q

How would you go about drawing an isomer from a name?

A

Start from the back of the name, create the carbon skeleton and work backwards through the name