OCR AS Chemistry

Topic Questions

4.6 Organic Synthesis

11 mark

The preparation of organic liquids, such as some esters, can involve heating under reflux.

Which statement about heating under reflus is correct?

  • Organic liquids can be heated without evaporation taking place.

  • Organic liquids can be maintained at their boiling point for extended periods.

  • Heating is carried out using a water bath.

  • The apparatus is closed to prevent the loss of any materials.

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21 mark

Which of the following can be done with the aid of a separating funnel?

  Neutralise acidic impurities Dry organic liquids Separate miscible liquids
A
B X
C X
D X X

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31 mark

What reaction could the following equipment be used for?

distillation

  • Preparing a carboxylic acid.

  • Cracking an alkane.

  • Oxidising an alcohol.

  • Halogenation of an alkene.

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41 mark

What is the purpose of the part labelled X in the diagram?

distillation---thermometer-labelled-x

  • To check the boiling point of the reaction mixture.

  • To separate the distillate from the reaction mixture.

  • To check the purity of the distillate.

  • To prevent gases from escaping.

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51 mark

Which type of reaction has the greatest atom economy?

  • Substitution

  • Hydrolysis

  • Elimination

  • Addition

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61 mark

Which reaction occurs when ethane and chlorine are mixed in the presence of sunlight?

  • A free-radical substitution with hydrogen produced

  • A free-radical substitution with hydrogen chloride produced

  • A free-radical substitution with no gas produced

  • A nucleophilic substitution with hydrogen chloride produced

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71 mark

This molecule is responsible for the flavour of spearmint chewing gum.

functional-group-mechanisms

What is a true statement about the functional groups 1 or 2?

  • 1 will undergo electrophilic addition

  • 1 will undergo electrophilic substitution

  • 2 will undergo nucleophilic substitution

  • 2 will undergo electrophilic substitution

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81 mark

The addition of hydrogen bromide, HBr, to pent-2-ene, CH3CH2CH2CH=CH2 , produces

  • 1-bromopentane

  • 2-bromopentane

  • 1,2-dibromopentane

  • A mixture of 1-bromopentane and 2-bromopentane

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91 mark

A reaction scheme is shown below. 

major-and-minor-product

Which of the following statements is correct?

  • Product 1 is the major product

  • Product 2 is the major product

  •  A 50:50 mixture of the two products is formed

  • The bromine acts as an electrophile

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101 mark

A reaction sequence is shown below. 

reaction-sequence

Identify reaction 1 and 2. 

  Reaction 1  Reaction 2 
A Nucleophilic Addition Oxidation
B Nucleophilic Substitution Oxidation
C Nucleophilic Addition Reduction
D Nucleophilic Substitution Reduction

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11 mark

Which statements about the preparation and purification of an organic liquid is/are correct?

  1. Reflux is used for the condensation reaction between an alcohol and a carboxylic acid.
  2. In a separating funnel, adding water will identify the organic layer as it will decrease in volume.
  3. A bunsen burner must be used in reflux because it requires more vigorous heating.
  • 1, 2 and 3

  • Only 1 and 2

  • Only 2 and 3

  • Only 1

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21 mark

Alcohol is produced by the following 2-step process.

Methylbutane rightwards arrow with bold Step bold space bold 1 on top Intermediate X begin mathsize 16px style rightwards arrow with bold Step bold space bold 2 on top end style Alcohol

Upon addition of acidified potassium dichromate(VI), the alcohol produces an orange solution.

Which row correctly identifies intermediate X and the reagents/conditions of step 2 in this process?

 

 

Intermediate X

Reagents/conditions of step 2

A

2-chloro-2-methylbutane

NaOH (aq) / reflux

B

2-methylbut-1-ene

NaOH (aq) / reflux

C

3-methylbut-1-ene

Steam and H2SO4 / heat

D

2-chloro-3-methylbutane

Steam and H2SO4 / heat

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31 mark

1-chlorobutane can be made by the following multistep process.

Which of the following reagents is not suitable for the indicated step?

vuqMYbi5_ocr-as-4-6h-mcq-q3-reaction-sequence

  • Step 1 hot K2Cr2O7/H2SO4

  • Step 2 hot Al2O3

  • Step 3 H2 and Ni catalyst

  • Step 4 Cl2 and UV light

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41 mark

Which of the following types of reaction is not involved in the sequence below?

rJyXzIce_ocr-as-4-6h-mcq-q4-reaction-sequence

  • Electrophilic addition

  • Elimination

  • Nucleophilic substitution

  • Free radical substitution 

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51 mark

Which of the following statements is/are correct?

  1. The sequence alkene → alcohol → aldehyde has a higher yield than alkene → haloalkane → alcohol → aldehyde.
  2. A nucleophile will attack a haloalkane because the halogen atom is more electronegative than the hydrogen atoms.
  3. Polyethene is not degraded by NaOH because of the electron-rich carbon-carbon double bonds.
  • 1, 2 and 3

  • Only 1 and 2

  • Only 2 and 3

  • Only 1

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11 mark

Crotonaldehyde, CH3CH=CHCHO, occurs in soybean oils and can be formed from its alcohol.

What are the reagents and conditions required to form crotonaldehdye from its alcohol?

  Reflux Distillation K2Cr2O7  K2Cr2O7 / H+ 
A X X
B X X
C X X
D X X

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21 mark

Which of the following reagents can be used to dry a damp sample of ethyl ethanoate?

  • Saturated sodium carbonate solution.

  • Anhydrous sodium sulfate.

  • Concentrated sulfuric acid.

  • Aluminium oxide.

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31 mark

Which molecule contains an aldehyde functional group?

  • CH3CH2CH2COOCH3 

  • CH3CH2CH2COCH3 

  • CH3CH2OCH2CH3 

  • CH3CH2CH2CH2CHO

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41 mark

Which haloalkane contains a tertiary carbon atom?

  • CH3CH2CH2Cl

  • CH3CH2CH(CH3)Br

  • C(CH3)3Cl

  • CH3CHBrCH2CH3 

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51 mark

Butanoic acid can be synthesised using the following two-step reaction scheme.

straight C subscript 4 straight H subscript 9 Br rightwards arrow with Step space 1 on top straight C subscript 4 straight H subscript 9 OH rightwards arrow with Step space 2 on top straight C subscript 3 straight H subscript 7 COOH

What is the correct classification of the steps?

  Step 1 Step 2
A Substitution  Addition
B Oxidation Substitution
C Addition Oxidation
D Substitution Oxidation

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61 mark

What reagents and conditions are required for the following two-step synthesis of propanal?

1-chloropropane rightwards arrow with Step space 1 on top Propan-1-ol rightwards arrow with Step space 2 on top Propanal

  Step 1 Step 2
A Reflux with NaOH (aq) Distil with K2Cr2O7 
B Reflux with NaCN (aq) Reflux with K2Cr2O7 / H+ 
C Distil with K2Cr2O7 / H+  Reflux with NaCN (aq)
D Reflux with NaOH (aq) Distil with K2Cr2O7 / H+ 

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71 mark

Butanone can be produced from but-1-ene by the following two-step synthesis of propanal.

But-2-ene rightwards arrow with Step space 1 on top INTERMEDIATE rightwards arrow with Step space 2 on top Butanone

Step 1 uses a phosphoric acid catalyst and steam.

What is the intermediate?

  • Butan-1-ol

  • Butan-2-ol

  • Butan-2,3-diol

  • Butanoic acid

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81 mark

The structure of a compound used to treat attention deficit hyperactivity disorder is shown below.

ocr-4-6m-q8

Which functional group(s) is / are in a molecule of the compound?

  1. Amine
  2. Carboxylic acid
  3. Ketone
  • 1, 2 and 3

  • Only 1 and 2

  • Only 2 and 3

  • Only 1

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91 mark

Ethane-1,2-diol can be made from ethene using the following two-stage synthetic route.

H2C=CH2 rightwards arrow with Step space 1 on top BrCH2CH2Br rightwards arrow with Step space 2 on topCH2OHCH2OH

What reagents are required for each step?

  Step 1 Step 2
A Excess HBr (aq)  Ethanolic NaOH
B Br2 (aq) C2H5OH (l)
C H2 (g) with a Ni catalyst NaOH (aq)
D Br2 (aq)  NaOH (aq)

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101 mark

Ethane-1,2-diol can be made from ethene using the following two-stage synthetic route.

H2C=CH2 rightwards arrow with Step space 1 on top BrCH2CH2Br rightwards arrow with Step space 2 on topCH2OHCH2OH

What are the mechanisms involved in each step?

  Step 1 Step 2
A Electrophilic substitution  Electrophilic addition
B Electrophilic addition Nucleophilic substitution
C Electrophilic addition Nucleophilic addition
D Nucleophilic substitution Electrophilic addition

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