Lesson 6.1.2
6.1.2 Carbonyl compounds Quiz: OCR Chemistry, Unit 5
20 questions
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Lesson 6.1.2, Carbonyl compounds: 20 multiple choice questions for the OCR Chemistry (H432), Unit 5: Organic chemistry and analysis, written with Revision Ninja.
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The 20 questions
-
What is the product when an aldehyde is oxidised by acidified potassium dichromate(VI)?
- A primary alcohol
- A carboxylic acid
- An ester
- A ketone
-
What is the product of the reaction of a carbonyl compound with HCN, through NaCN(aq) and H+(aq)?
- A carboxylic acid
- An amine
- An alkene
- A hydroxynitrile
-
Which species acts as the initial nucleophile in the addition of HCN to an aldehyde?
- Hydride ion
- Hydrogen ion
- Nitrogen atom
- Cyanide ion
-
An orange precipitate with 2,4-dinitrophenylhydrazine indicates the presence of which functional group?
- Carbonyl group
- Carboxyl group
- Ester group
- Hydroxyl group
-
How can a purified 2,4-DNP derivative be used to identify a specific aldehyde or ketone?
- Measure melting point
- Measure boiling point
- Determine molar mass
- Measure optical rotation
-
What visual observation occurs when an aldehyde is warmed with Tollens' reagent?
- Orange precipitate
- Blue solution
- Effervescence
- Silver mirror
-
What is observed when a ketone is heated with Tollens' reagent?
- Red precipitate
- No reaction
- Silver mirror
- Gas evolution
-
What is the product when propanal reacts with NaBH4 and then water?
- Propanoic acid
- Propan-2-ol
- Propan-1-ol
- Propanone
-
What is the product when propanone reacts with NaBH4 and then water?
- Propan-1-ol
- Propan-2-ol
- Propanoic acid
- Propanal
-
What is the product when ethanal reacts with HCN and then the nitrile is considered?
- Ethanoic acid, CH3COOH
- 2-hydroxypropanenitrile, CH3CH(OH)CN
- Propanenitrile, CH3CH2CN
- Ethylamine, CH3CH2NH2
-
Ethanal is oxidised with acidified dichromate. What colour change is seen?
- Orange to green
- Green to orange
- Yellow to purple
- Colourless to blue
-
Which type of reaction occurs when HCN reacts with an aldehyde?
- Nucleophilic substitution
- Free radical substitution
- Nucleophilic addition
- Electrophilic addition
-
What product mixture is formed when HCN adds to ethanal?
- Geometric isomers
- Racemic mixture
- Structural isomers
- Single enantiomer
-
What is the product of propanone reacting with HCN, followed by acid hydrolysis of the nitrile?
- 2-methylpropanoic acid
- 2-hydroxy-2-methylpropanoic acid
- Propan-2-ol
- Propan-2-amine
-
An unknown compound forms an orange precipitate with 2,4-DNP but no mirror with Tollens' reagent. What is it?
- An aldehyde
- An alcohol
- A ketone
- A carboxylic acid
-
Which species acts as the nucleophile in the reduction of aldehydes using NaBH4?
- Hydroxide ion
- Hydronium ion
- Sodium ion
- Hydride ion
-
What is the product of reducing butanone with NaBH4 followed by water?
- Butan-2-one
- Butan-2-ol
- Butan-1-ol
- Butanoic acid
-
What is the product of reducing phenylethanone (acetophenone) with NaBH4 followed by water?
- 1-phenylethanol
- Phenylethanoic acid
- Ethylbenzene
- 2-phenylethanol
-
Which organic ion is formed when benzaldehyde is oxidised by Tollens' reagent before acidification?
- Phenoxide ion
- Benzoate ion
- Benzyl ion
- Benzoyl ion
-
Which intermediate ion is formed immediately after nucleophilic attack on a carbonyl compound by CN⁻?
- Carbocation
- Carbanion
- Hydroxide ion
- Alkoxide ion
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