6. Organic molecules (ALCOHOLS) Flashcards

1
Q

Give the 3 types of alcohols you can form

A

Primary - 1 carbon attached to the carbon adjoining the O-H
Secondary - 2 carbons attached to the carbon adjoining the O-H
Tertiary - 3 carbons attached to the adjoining the O-H

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2
Q

Give the oxidation agent used for oxidising alcohols

A

Potassium or Sodium dichromate

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3
Q

Give the symbol for an oxidising agent

A

[O]

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4
Q

What are primary alcohols oxidised to

A

Aldehydes (after immediate distillation) , then carboxylic acids (under reflux)
(remember to add H2O)

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5
Q

Give the colour change for the oxidation of primary alcohols

A

Orange to green

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6
Q

How many oxidising agents do you need for reflux for carboxylic acids

A

2 [O]

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7
Q

What are secondary alcohols oxidised to

A

Ketones

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8
Q

What are tertiary alcohols oxidised into

A

Nothing, they cannot be oxidised

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9
Q

Describe Fehling’s test in order to distinguish between a aldehyde ( O double bonded to C, single bonded to H) or a ketone (O double bonded to C in the middle of the chain)

A

1) add Fehlings solution to the test tube
2) needs to be warmed in alkaline conditions
3) if an aldehyde is present a brick red precipitate forms
4) ketones don’t give a positive result

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10
Q

What is the condition required and product of dehydrating an alcohol

A

Produces an alkene –> The alcohol is heated with hot concentrated phosphoric acid- H2SO4
(elimination reaction) and removes a molecule of water

Dehydration of primary alchol produces a single alkene
Dehydration of secondary alchol produces a mixture of alkenes

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11
Q

Describe the process of distillation

A

1) heat liquids in a pear shaped flask and lowest boiling point will evaporate first
2) rises out of flask and into a condenser
3) liquid condensed and is collected in a separate flask

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12
Q

Which way does the water come in from in a condenser

A

Top - out
Bottom - in
–> this ensures water fills up the condensor

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13
Q

Describe how to produce chloroalkanes from alcohols

A

React the alcohol with PCl5
- HCl and POCl3 are also formed

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14
Q

Describe how to produce bromoalkanes from alcohols

A

React the alcohol with HBr (formed by reacting 50% conc sulfuric acid with KBr)
- also forms H2O

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15
Q

Describe how to produce idoalkanes from alcohols

A

React alcohol with PI3 (formed by reacting red phosphorous with Iodine, I2)
- also forms H3PO3

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16
Q

Using the apparatus for distillation instead of reflux is not an efficient way to produce
ethanoic acid from ethanol. Explain why.

A

Because ethanol will be oxidised into ethanal as that has a lower boiling point than ethanoic acid

17
Q

Explain the purpose of anti bumping crystals in distillation or reflux

A

Prevents large bubbles from forming

18
Q

Describe important features of a diagram showing reflux or distillation

A

Have to show the separate apparatus being joined
Thermometer in distillation must be opposite the entrance of the lieburg condenser during distillation
Cant be a gap
Should not be a bung on reflux as pressure builds up

19
Q

What is reflux

A

continuous evaporating and condensation