Alcohols Flashcards

(31 cards)

1
Q

Name the two industrial methods of making alcohols

A

Hydration of ethene, Fermenting glucose

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2
Q

What are the 3 conditions needed for the hydration of ethene

A

A phosphoric catalyst (H₃PO₄), 300°C, 60 atm

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3
Q

What are the two conditions needed for fermenting glucose

A

Yeast, 37°C.

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4
Q

How do you turn alkanes to alkenes to hydrate them

A

You have to crack the alkanes to get alkenes

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5
Q

Outline the method for fermenting glucose to make alcohol

A

All oxygen is used aerobically, then anaerobic respiration kicks in creating bubbles of CO₂.
Ethanol is toxic therefore killing all the yeast cells.

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6
Q

What is the percentage yield of fermenting glucose

A

10%

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7
Q

How do you improve the yield of fermenting glucose

A

Before all the glucose is used you distil the ethanol then add excess glucose to continue the reaction

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8
Q

What are the advantages of the hydration of ethene

A

100% atom economy, It’s a continuous process

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9
Q

What are the disadvantages of the hydration of ethene

A

-Hard to reach 300°C and 60 atm
-Burning crude oil (greenhouse gas CO₂)
-Not sustainable, non-renewable

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10
Q

What are the advantages of the fermentation of glucose

A

-Sustainable, renewable
-Carbon neutral (to a point)

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11
Q

What are the disadvantages of the fermentation of glucose

A

-lower atom economy
-Expensive
-batch process
-ethanol is toxic therefore breaking

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12
Q

what do you need to oxidise an alcohol

A

an oxidising agent [O] known as acified potassium dichromate (VI). also written as H⁺/K₂Cr₂O₇

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13
Q

What colour is acified potassium dichromate (VI)

A

It starts as orange is goes green when reduced

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14
Q

What are the products when oxidising a primary alcohol

A

You get an aldehyde, and when you oxidise the aldehyde you get a carboxylic acid, and H₂O

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15
Q

What are the products when a secondary alcohol is oxidised

A

a Ketone + H₂O

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16
Q

What are the products when oxidising a tertiary alcohol

A

Nothing, they cannot be oxidised

17
Q

What is a tertiary alcohol

A

an alcohol where the carbon that’s connected to the (OH) functional group is also attached to 3 other carbons

18
Q

If you want to get an aldehyde from a primary alcohol what practical do you have to carry out

A

A Distillation

19
Q

What practical do you have to carry out to oxidise an aldehyde to a carboxylic acid

20
Q

What is the functional group present in alcohols?

A

-OH functional group known as the hydroxyl group.

21
Q

What is the simplest alcohol and its uses?

A

Methanol is the simplest alcohol, used as a fuel and an important chemical feedstock.

22
Q

What are some products that use methanol as a starting material?

A

Methanol is used in polymers, paints, solvents, insulation, adhesives, and many other useful products.

23
Q

What is the second member of the alcohol homologous series?

A

Ethanol, primarily used in alcoholic drinks.

24
Q

What is the first step in naming alcohols?

A

Count the number of carbons and name accordingly.

25
What prefixes are used for alcohols with more than one -OH group?
Use the prefixes di, tri, tetra.
26
What should you consider when naming alcohols?
Look at the name of the -OH and what carbon they are bonded to, and look for any branches.
27
What type of bond do alcohols have due to electronegativity differences?
Alcohols have a polar O-H bond.
28
What type of intermolecular forces are present in alcohols?
Stronger intermolecular forces due to hydrogen bonding, but London forces are weak like in alkanes.
29
How can alcohols be classified?
Alcohols can be classified as primary, secondary, or tertiary.
30
What defines a primary alcohol?
A primary alcohol has 2 hydrogens attached to the carbon atom with the functional group (except methanol).
31
What defines a secondary alcohol?
A secondary alcohol has 1 hydrogen attached to the carbon atom with the functional group.