Alcohols Flashcards

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

A

Reflux

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
Q

What prefixes are used for alcohols with more than one -OH group?

A

Use the prefixes di, tri, tetra.

26
Q

What should you consider when naming alcohols?

A

Look at the name of the -OH and what carbon they are bonded to, and look for any branches.

27
Q

What type of bond do alcohols have due to electronegativity differences?

A

Alcohols have a polar O-H bond.

28
Q

What type of intermolecular forces are present in alcohols?

A

Stronger intermolecular forces due to hydrogen bonding, but London forces are weak like in alkanes.

29
Q

How can alcohols be classified?

A

Alcohols can be classified as primary, secondary, or tertiary.

30
Q

What defines a primary alcohol?

A

A primary alcohol has 2 hydrogens attached to the carbon atom with the functional group (except methanol).

31
Q

What defines a secondary alcohol?

A

A secondary alcohol has 1 hydrogen attached to the carbon atom with the functional group.