4.2 Alcohols, Haloalkanes and Analysis (started) Flashcards

4.2.1 Alcohols 4.2.2 Haloalkanes 4.2.3 Organic synthesis 4.2.4 Analytical techniques

1
Q

How do alcohols boiling points compare to similar sized alkanes?

A

Higher as alcohols have hydrogen bonds between molecules

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2
Q

What internolecular forces are present in alcohols?

A

Hydrogen bonds between formula groups

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3
Q

What is a primary, secondary and tertiary alcohol?

A

1° Primary - end of the carbon chain
2° Secondary - middle of the carbon chain
3° Tertiary - middle with another branch attached of the carbon chain

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4
Q

What are the products of a combustion of an alcohol?

A

Carbon dioxide and water

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5
Q

What is the general formula for an alcohol?

A

Cn H2n+1 OH

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6
Q

What is the oxidising agent used to oxidise primary and secondary alcohols?

A

Acidified potassium dichromate

H+/Cr2O7 2-

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7
Q

How are oxidising agents represented in chemical equations?

A

[O]

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8
Q

How do you produce an aldehyde?

A

Oxidise a primary alcohol by distillation
Produces water as well
Colour change from orange to green

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9
Q

How do you produce a carboxylic acid?

A

Further oxidise an aldehyde
Reflux a primary alcohol
Produces water as well (only from alcohol not from aldehyde)
Colour change from orange to green

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10
Q

How do you produce a ketone?

A

Oxidise a secondary alcohol by reflux
Produces water as well
Colour change from orange to green

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11
Q

What happens when you react tertiary alcohols with acidified potassium dichromate?

A

Nothing happens

Colour remains orange

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12
Q

What is reflux?

A

Continual boiling and condensing of a reaction mixture to ensure the reaction goes to completion without the mixture boiling dry

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13
Q

What is distillation?

A

The technique of heating a liquid to create vapour which is collected when cooled seperate from the original liquid

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14
Q

What is an elimination reaction?

A

Dehydration an alcohol to form an alkene and water
Conc sulphuric acid
Heat
Reflux

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15
Q

How do alcohols produce a haloalkane?

A

Substitution in the presence of an acid

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16
Q

Why do you use infra red for spectrometry instead of ultra violet?

A

Ultra violet will break the bonds

17
Q

What happens if you shine the right amount of energy on a bond with infra red energy?

A

You can kick it into a higher state of vibration

The amount of energy needed will change and each bond will absorb a different frequency

18
Q

What are applications of infra red spectroscopy?

A

Breathalysers

Monitoring air pollution

19
Q

How do breathalysers work?

A

Identifying ethanol by absorbance in C-O O-H bonds

Identifying amount of ethanol by amount if IR absorption

20
Q

What bonds do the common greenhouse gases contain that can be found in IR sprectroscopy?

A

Carbon Dioxide C=O bonds
Water vapour O-H bonds
Methan C-H bonds

21
Q

What is the moleculer ion peak?

A

Furthest right peak which is the Mr of the molecuke

22
Q

Why could there be smaller peak just to the right of the molecular ion peak?

A

Due to a Carbon 13 isotope which will increase the Mr

23
Q

What does each peak show on a mass spectrometer?

A

Positive ions from fragments of molecule

e.g. CH3OCH3 can have fragments at 31for [CH3O]+ and 15 [CH3]+

24
Q

How does the rate of hydrolysis of a haloalkane depend on the halogen present?

A

The weaker the bond the faster the rate of reaction

C-I is the weakest and therefore fastest, rate decreases up the group