CbD - Organic reactions Flashcards

1
Q

What 7 types can organic chemistry reactions be classified into?

A
addition
elimination
substitution
condensation
hydrolysis
oxidation
reduction
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2
Q

Addition

A

2 molecules join together to form a single product. Involves breaking a double bond.

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3
Q

Elimination

A

Involves removing a functional group which is released as a part of a small molecule. Often a double bond is formed.

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4
Q

Substitution

A

A functional group on a molecule is swapped for a new one.

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5
Q

Condensation

A

2 molecules get joined together with the loss of a small molecule, e.g. water. The opposite of hydrolysis.

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6
Q

Hydrolysis

A

Water is used to split apart a molecule creating two smaller ones. Opposite of condensation.

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7
Q

Oxidation

A

Oxidation is loss of electrons. In organic chemistry it usually means gaining an oxygen atom or losing a hydrogen atom.

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8
Q

Reduction

A

Reduction is gain of electrons. In organic chemistry it usually means gaining a hydrogen atom or losing an oxygen atom.

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9
Q

What does bromine water test for?

A

Alkenes

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10
Q

What is used to test for alkenes?

A

Bromine water

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11
Q

What are you actually testing for when testing whether something is an alkene using bromine water?

A

The presence of double bonds.

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12
Q

Explain how bromine water is used to test for alkenes

A

1) Add 2cm3 of the solution that you want to test to a test tube.
2) Add 2cm3 of bromine water to the test tube.
3) Shake the test tube.

Alkene = the solution will decolourise (go from orange to colourless).
Not alkene = nothing happens.

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13
Q

What colour is bromine water?

A

Orange

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14
Q

Positive test with bromine water

A

Alkene = the solution will decolourise (go from orange to colourless).

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15
Q

Explain how you test whether an alcohol is a primary, secondary or tertiary alcohol?

A

1) Add 10 drops of the alcohol to 2cm3 of acidified potassium dichromate solution in a test tube.
2) Warm the mixture gently in a hot water bath.
3) Then watch for a colour change.

Primary = the orange solution slowly turns green as an aldehyde forms. (If you carry on heating, the aldehyde will be oxidised further to give a carboxylic acid.)

Secondary = the orange solution slowly turns green as a ketone forms.

Tertiary = nothing happens.

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16
Q

What happens when you mix acidified potassium dichromate(VI) solution with a primary alcohol?

A

Primary = the orange solution slowly turns green as an aldehyde forms. (If you carry on heating, the aldehyde will be oxidised further to give a carboxylic acid.)

17
Q

What happens when you mix acidified potassium dichromate(VI) solution with a secondary alcohol?

A

Secondary = the orange solution slowly turns green as a ketone forms.

18
Q

What happens when you mix acidified potassium dichromate(VI) solution with a tertiary alcohol?

A

Tertiary = nothing happens.

19
Q

What causes the colour change when alcohols (primary and secondary) are mixed with acidified potassium dichromate(VI) solution?

A

The colour change is the orange dichromate(VI) ions (Cr2O7^2-) being reduced to the green chromium(III) ion (Cr^3+).

20
Q

What is the downside to testing for which sort of alcohol you have using acidified potassium dichromate(VI) solution?

A

The result for primary and secondary alcohol is the same.

21
Q

How do you test whether something is a primary or secondary alcohol?

A

1) Add excess alcohol to 2cm3 of acidified potassium dichromate(VI) solution in a round bottomed flask.
2) Set up the flask as part of distillation apparatus.
3) Gently heat the flask. The alcohol will be oxidised and the product will be distilled off immediately so you can collect it.
4) Once you have collected the product, you need to test it to find out if it is an aldehyde or a ketone using Tollens reagent or Fehling’s solution. If it is an aldehyde, you started with a primary alcohol. If it is a ketone, you started with a secondary alcohol.

22
Q

What do you use to oxidise alcohols?

A

Acidified potassium dichromate(VI).