alcohols Flashcards

(71 cards)

1
Q

what is the definition of biofuel?

A

a fuel produced from plants or other living matter

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2
Q

what is the definition of carbon neutral?

A

an activity that has no net annual carbon emissions to the atmosphere

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3
Q

what is the definition of oxidation?

A

loss of electrons, gain of oxygen, loss of hydrogen

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4
Q

what is the definition of oxidising agent?

A

a substance which is reduced so another substance can be oxidised

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5
Q

position isomer

A

structural isomers that differ by having the functional group in a different position

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6
Q

what is the definition of reduction

A

gain of electrons, loss of oxygen, gain of hydrogen

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7
Q

what is the definition of reducing agent

A

a substance which is oxidised so that another substance can be reduced

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8
Q

what is the definition of reflux?

A

heating a reaction mixture while continually cooling the vapour produced back into the liquid form using a condenser

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9
Q

what is stereoisomer?

A

molecules with the same molecular and structural formulae but a different spatial arrangement of atoms

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10
Q

what is structural isomer

A

molecules with the same molecular formular but different structures

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11
Q

what is the definition of unsaturated

A

molecule containing double bonds

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12
Q

What is the general formula for alcohols?

A

CnH2n+1 OH

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13
Q

How can the formula for alcohols be shortened?

A

ROH

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14
Q

What is the first step in naming alcohols?

A

Identify the parent alkane

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15
Q

What should you find when identifying the parent alkane?

A

The longest continuous carbon chain containing the hydroxyl group (-OH)

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16
Q

What is the second step in naming alcohols?

A

Replace the ‘-e’ ending of the parent alkane name with ‘-ol’

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17
Q

If the parent alkane is ‘propane’, what is the name of the corresponding alcohol?

A

Propanol

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18
Q

What is the third step in naming alcohols?

A

Number the carbon atoms in the chain

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19
Q

Why is it important to number the carbon atoms in the alcohol chain?

A

So that the hydroxyl group (-OH) has the lowest possible number

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20
Q

What do alcohol groups have priority over in naming?

A

Carbonyl groups

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21
Q

How do you indicate the position of the hydroxyl group in the alcohol name?

A

Use a number to indicate the position of the hydroxyl group

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22
Q

If the hydroxyl group is on the second carbon, how would you name the alcohol?

A

Propan-2-ol

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23
Q

What should you do if there are other substituents on the carbon chain?

A

Name them as usual and include their positions using numbers

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24
Q

How should substituents be ordered in the naming of alcohols?

A

List substituents in alphabetical order

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25
What prefixes are used to indicate the number of hydroxyl groups in a compound?
Di, tri, tetra ## Footnote These prefixes indicate two, three, and four hydroxyl groups, respectively.
26
What is the bond angle in alcohols?
105° ## Footnote This angle is due to the arrangement of bonding and lone pairs around the oxygen atom.
27
Why is the bond angle in alcohols reduced from the ideal tetrahedral angle?
Lone pairs repel more than bonding pairs ## Footnote This leads to a position of minimum repulsion, resulting in a smaller bond angle.
28
What defines a primary alcohol (1º)?
The carbon atom bonded to the -OH group is attached to one other carbon atom ## Footnote Primary alcohols have the general formula R-CH2OH.
29
How is a secondary alcohol (2º) characterized?
The carbon atom bonded to the -OH group is attached to two other carbon atoms ## Footnote Secondary alcohols have the general formula R-CHOH-R'.
30
What distinguishes a tertiary alcohol (3º)?
The carbon atom bonded to the -OH group is attached to three other carbon atoms ## Footnote Tertiary alcohols have the general formula R-COH(R')2.
31
What type of molecules are alcohols?
Polar molecules ## Footnote Alcohols have a -OH group which contributes to their polarity.
32
What causes the partial positive charge in alcohols?
The highly electronegative O atom in the -OH group pulls electron density away from adjacent H and C atoms ## Footnote This results in a polar bond.
33
What type of bonds can form between alcohol molecules?
Hydrogen bonds ## Footnote These bonds lead to higher melting and boiling points compared to alkanes.
34
How does the presence of the alcohol group affect solubility in water?
It makes short-chain alcohols like methanol and ethanol soluble in water ## Footnote The ability to form hydrogen bonds with water contributes to this solubility.
35
What interactions do alkyl chains form?
Weak instantaneous temporary dipole-dipole interactions ## Footnote Alkyl chains are non-polar and do not form hydrogen bonds.
36
What happens to the effects of the alcohol group as the chain length increases?
The unique effects of the alcohol group become less prominent ## Footnote Longer carbon chains lead to decreased solubility in water.
37
What is the state of ethane at room temperature?
Gas ## Footnote Ethane cannot form hydrogen bonds like ethanol.
38
What is the state of ethanol at room temperature?
Liquid ## Footnote Ethanol forms hydrogen bonds which require more energy to overcome.
39
What type of interactions exist in ethane compared to ethanol?
Instantaneous temporary dipole-dipole interactions ## Footnote These are weaker than hydrogen bonds in ethanol.
40
Why does ethanol have a higher boiling point than ethane?
Ethanol requires more energy to overcome hydrogen bonds ## Footnote Higher thermal energy is needed due to stronger intermolecular forces.
41
Fill in the blank: Alcohols form _______ with other alcohol molecules.
Hydrogen bonds
42
What do alcohols produce when they undergo complete combustion?
Carbon dioxide and water ## Footnote The reaction is represented as: alcohol + oxygen → carbon dioxide + water.
43
What type of flame do smaller alcohols burn with?
An almost invisible flame
44
How can ethanol be produced sustainably?
By the fermentation of sugars
45
What is the energy density of ethanol compared to petrol?
Lower than petrol
46
What must cars running on ethanol have due to its lower energy density?
A larger fuel tank or fill up more often
47
What is the benefit of blending ethanol with petrol or diesel?
Increases energy density and makes flames easier to see
48
What socio-economic concern is associated with using large quantities of farmland for ethanol production?
It could be better used for food production
49
Fill in the blank: Alcohols react with oxygen in the air when ignited and undergo complete combustion to form _______.
carbon dioxide and water
50
True or False: The combustion of alcohols produces heat.
True
51
What happens to alcohols during oxidation?
They can be oxidised to other products depending upon the type of the alcohol.
52
What is an oxidising agent?
A substance that oxidises another.
53
How is oxidation shown in an equation?
By using [O].
54
What is a common oxidising agent used in oxidation reactions?
Acidified dichromate (VI) ions, H+/Cr2O7^2-.
55
What is the typical form in which acidified dichromate (VI) ions are provided?
In the form of sulphuric acid mixed with potassium dichromate solution.
56
What color are potassium dichromate (VI) ions?
Orange.
57
To what color are dichromate (VI) ions reduced?
Green chromium (III) ions (Cr3+).
58
What does the reduction of dichromate (VI) ions indicate?
They are acting as oxidising agents.
59
What is the color of acidified potassium manganate(VII)?
Purple.
60
What is required for the reduction of potassium manganate(VII) to take place?
An acidic medium.
61
What happens to the purple manganate ions during alcohol oxidation?
They are reduced to colourless Mn^2+ ions.
62
What can primary alcohols be oxidised to form?
Aldehydes ## Footnote Aldehydes can undergo further oxidation to form carboxylic acids.
63
What do secondary alcohols oxidise to form?
Ketones only
64
Do tertiary alcohols undergo oxidation?
No
65
What is the first step in the oxidation of primary alcohols?
The primary alcohol is added to the oxidising agent and warmed
66
What happens to the boiling points of aldehydes compared to primary alcohols?
The aldehyde product has a lower boiling point than the alcohol reactant
67
What occurs if the aldehyde is not distilled off during oxidation?
Further refluxing with excess oxidising agent will oxidise it to a carboxylic acid
68
What must be done with the ketone product after it has been formed?
It does not need to be distilled off straight away
69
Fill in the blank: Tertiary alcohols do not undergo _______.
Oxidation
70
True or False: Aldehydes can be further oxidised to form carboxylic acids.
True
71
True or False: Secondary alcohols can be oxidised to form carboxylic acids directly.
False