TOPIC 17 - Organic chemistry II Flashcards

1
Q

What are optical isomers?

A

Mirror images of each other that have a chiral carbon.

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2
Q

What is a chiral molecule?

A

Molecule that has 4 different groups attached to a carbon atom. These groups can be arranged in two different ways (enantiomers).

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3
Q

What are enantiomers?

A

Isomers that are non-superimposable images of each other.

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4
Q

Draw the two enantiomers of this molecule

A
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5
Q

What is plane polarised light?

A

Light that only oscillates in one plane.

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6
Q

One enantiomer rotates plane polarised light 10º clockwise. What effect does the other enantiomer have?

A

Rotates plane polarised light 10º anticlockwise.

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7
Q

What are racemates?

A

Racemic mixtures, which are mixtures that are made from a equal amount of enantiomer.

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8
Q

Do racemates rotate plane polarised light?

A

No. The 2 enantiomers have opposite effects and so cancel out.

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9
Q

How can SN1 reactions produce racemic mixtures?

A
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10
Q

How can SN2 reactions produce only 1 enantiomer?

A
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11
Q

What is the boiling point for aldehydes + ketones in comarison to alcohols?

A

Lower bpts than alcohols.

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12
Q

Can aldehydes+ketones hydrogen bond with water?

A

Yes

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13
Q

Can aldehydes+ketones dissolve in water? Why?

A

Yes. But only the small ones since with bigger ones, London forces between the hydrocarbon chains become stronger than the H-bonding with water and so they don’t dissolve.

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14
Q

How can we distinguish between aldehydes and ketones using K2Cr2O7 ?

A

Aldehydes are oxidised by K2Cr2O7, while ketones aren’t.

If aldehyde is present solution turns from orange (Cr2O7 2-) to green (Cr3+). If ketone is present, there’s no change.

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15
Q

How can we use Tollen’s reagent to distinguish between aldehydes and ketones?

A
  • Place aldehyde/ketone in hot water bath with Tollen’s reagent.
  • No bunsen burner because aldehydes/ketones are flammable.
  • If aldehydes are present, a silver coating is seen.
  • If ketones present, no change.
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16
Q

How is Tollen’s reagent made?

A

Reacting silver nitrate with aqueous ammonia.

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17
Q

What is the general equation for the reaction of Tollen’s reagent with an aldehyde?

A
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18
Q

How can we use Fehling’s or Benedict’s slution to distinguish between aldehydes and ketones?

A

Add both solutions to warm water bath.

If aldehyde present, solution turns from blue to a brick red precipitate (Cu2O).

If ketones are present, there’s no change.

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19
Q

What is the difference between Fehling’s and Benedict’s solution?

A
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20
Q

What is the equation for the reaction of Fehling’s / Benedict’s solution with aldehyde?

A
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21
Q

What are the conditions for the reduction of aldehydes and ketones into alcohols?

A

NaBH4 dissolved in methanol and water.

22
Q

What is the mechanism for the reaction between carbonyl compounds and potassium cyanide?

A
23
Q

What type of mechanism is the reaction between carbonyl compounds and potassium cyanide to form hydroxynitriles?

A

Nucleophilic addition.

24
Q

Can hydrogen cyanide (instead of potassium cyanide) react with a carbonyl group to give a hydroxynitrile?

A

Yes. But no acid is needed.

25
Q

What are the risks when using potassium cyanide? What precautions must be taken?

A
26
Q

How can 2,4-dinitrophenylhydrazine (Brandy’s reagent) be used to identify a carbonyl group?

A
27
Q

Which type of carbonyl groups react with iodine?

A

Only the ones that have a methyl group (CH3) attached.

28
Q

How can iodine be used to identify a carbonyl group that’s attached to a CH3?

A
29
Q

What is the equation for the reaction between iodine and a carbonyl attached to a CH3?

A
30
Q

Are carboxylic acids soluble in water?

A

Only the smaller ones.

31
Q

What are carboxylic acid dimers?

A
32
Q

What is the equation for the hydrolysis of nitriles to give a carboxylic acid?

A
33
Q

What is the equation for the reaction of ethanoic acid and sodium carbonate?

A
34
Q

What is the equation for the reaction of ethanoic acid and sodium hydrogencarbonate?

A
35
Q

What are the conditions for the reduction of carboxylic acids into alcohols?

A

LiAlH4 in a dry ether solvent.

36
Q

What are the conditions for turning carboxylic acids into acyl chlorides?

A

React with phosphorous (V) chloride.

37
Q

What is the equation for the reaction of carboxylic acids with phosphorous (V) chloride?

A
38
Q

What is the catalyst used for the reaction between carboxylic acid and alcohol to give an ester and water?

A

Sulfuric acid.

39
Q

In esterification, how is the ester purified?

A
40
Q

What is the name of this ester?

A
41
Q

What is the name of this ester?

A
42
Q

What are the uses of ester?

A
43
Q

What is the equation for ester acid hydrolysis?

A
44
Q

What is the equation for ester base hydrolysis?

A
45
Q

Draw one repeating unit of this polyester

A
46
Q

What is the equation for the reaction that makes 1 repeating unit of the polyester Terylene?

A
47
Q

What is the equation for the reaction between ethanoyl chloride and H2O?

A
48
Q

What is the equation for the reaction between ethanoyl chloride and Ammonia?

A
49
Q

What is the equation for the reaction between ethanoyl chloride and alcohols?

A
50
Q

What is the equation for the reaction between ethanoyl chloride and primary amines?

A