You can get the Chemistry 2nd Year Aldehydes and Ketones MCQs with answers here. Aldehydes and Ketones are the organic compounds containing the carbonyl group. Both have different nomenclature. Aldehydes are manufactured in laboratories and Industries. There are various reactions to carbonyl compounds. The nucleophilic addition reactions take place in carbonyl compounds. The first one is Base-Catalysed Addition Reaction which includes Condensation reactions, Cannizzaro’s reaction, Haloform reaction. The second one is the Acid-Catalysed Addition reaction includes the Reaction of Addition of Alcohols and Ammonia Derivatives. Oxidation and Reduction Reactions are also very important to take place in Aldehydes and Ketones. Carbonyl compounds are identified using different tests. Aldehydes are used in the manufacture of different products. This chapter has a lot of importance with the entry test point of view. So, have a look at the important MCQs of this chapter.
Chemistry 2nd Year Aldehydes and Ketones MCQs

KEY POINTS
- Nomenclature of Aldehydes and Ketones
- Preparation of Aldehydes and Ketones
- Reactivity of Carbonyl Compounds
- Nucleophilic Addition reaction
- Reduction Reaction/Oxidation reaction
- Identification of Carbonyl Compounds
- Uses of Formaldehyde and Acetaldehyde
Question#1: Symmetrical structure of a ketone refers to:
- The uneven number of carbon atoms on either side of the carbonyl group
- The same number of carbon atoms on either side of the carbonyl group
- Just I carbon more on the right of the carbonyl group
- Just I carbon more on the left of the carbonyl group
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Question#2: Which of the following can be used for the oxidative preparation of aldehydes from alcohol?
- Pt-asbestos
- FeO and MO2O3
- Na2Cr2O7and h2SO4
- All of these
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Question#3: Ethylene is oxidized to acetaldehyde on a commercial scale by the use of the catalyst which is:
- PdCI2 and CuCI2
- FeO and Mo2O3
- Na2Cr2O7 and H2SO4
- All of these
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Question#4: The clear fact for the structural differences between aldehyde and ketone is:
- A ketone has one R group attached on the carbonyl group
- An aldehyde has two R groups attached on the carbonyl group
- An aldehyde has one R and a ketone has two R group attached to a carbonyl group
- Both A and C
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Question#5: Formation of yellow or orange /red precipitates with 2,4-DNPH refers to the identification of:
- Aldehydes
- Both A and C
- Ketones
- Pure alcohols only
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Question#6: An alcohol giving positive 2,4-DNPH test implies that:
- It is 100% pure
- It may contain some contents of aldehydes and ketones
- It is ethanol
- None of these
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Question#7: Reduction of an aldehyde using NaBH4gives:
- Primary alcohol
- Tertiary alcohol
- Secondary alcohol
- Phenol
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Question#8: Reduction of a ketone using NaBH4 gives:
- Primary alcohol
- Tertiary alcohol
- Secondary alcohol
- Phenol
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Question#9: HCN can be added to:
- Aldehydes
- Ketones
- Ethers
- Both A and C
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Question#10: Addition of HCN to acetaldehyde in the presence of dilute mineral acid and sodium cyanide forms:
- Formaldehyde cyanohydrins
- Acetone cyanohydrins
- Acetaldehyde cyanohydrin
- Butanone cyanohydrins
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Question#11: Acidified hydrolysis of cyanohydrins form.
- Carboxylic acids
- Hydroxyl-carboxylic acids
- Alcohols
- Aldols and ketols
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Question#12: Haloform test is given by:
- Acetaldehyde
- Propanone
- Melty group ketones
- All of these
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Question#13: CHX3 will be given by all the carbonyl compounds containing at least one:
- EthyI group
- IsopropyI group
- methyl group
- Both B and C are correct
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Question#14: In the oxidation of unsymmetrical ketones using strong oxidizing agents like conc.HNO3, which carbon atom is preferentially attacked:
- A carbon atom with the maximum number of hydrogen atoms
- A carbon atom with the least number of hydrogen atoms
- Alpha
- Beta carbon
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Question#15: Which of the following ketones will produce acid only after oxidation by acidified potassium dichromate?
- EthyI n-propyI ketone
- ethyl methyl ketone
- dimethyl ketone
- diethyl ketone
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Question#16: What will be the product in the following reaction?
CH3 CH=CHCH2 COCH3 ———?
- CH3CH2 CH2 CH2COCH3
- CH3 CH2 CH2 CH2CH(OH) CH3
- CH3 CH= CHCH2 CH(OH) CH3
- All of these
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Question#17: Which of the following will not form enolate ion?
- CH3COCH3
- CH3SwHO
- HCHO
- All of these
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Question#18: In this compound C1H2-C2CH3 the hybridization of carbon number 1 and carbon number 2.
- Sp3 ,Sp3
- Sp2 ,Sp2
- Sp2, Sp3
- Sp, Sp2
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Question#19: Which of the following has maximum steric hindrance?
- (C2H5)2CO
- CH3COCH3
- C3H7COCH3
- CH3COH
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Question#20: Which of the following has maximum reactivity in nucleophilic substitution reactions?
- Formaldehyde
- Acetaldehyde
- Propanone
- All of these
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Question#21: Formation of cyanohydrins form an aldehyde is an example of:
- Nucleophilic substitution
- Nucleophilic addition
- Electrophilic addition
- Electrophilic substitution
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Question#22: For which one of the following pairs of compounds can the members be distinguished by means of Tollen’s test.
- HCHO and CH3 CHO
- CH3CHO and CH3COCH3
- HCHO
- CH3 CH2 CH(CHO) CH3
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Question#23: All of the following react with Fehling solution except:
- CH3 CH2 Cho
- CH3 CH2COCH3
- HCHO
- CH3 CH2 CH(CHO) CH3
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Question#24:Which of the following will not give an iodoform test?
- Ethanol
- Ethanol
- 3-pentanone
- 2-pentanone
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Question#25: Which substance does not oxidize easily?
- CH3 CH2CHO
- CH3 CHO
- HCHO
- CH3COCH3
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Question#26: Which one of the following sets of compounds oxidizes aldehydes as well as ketones?
- CuSO4+NaOH+Citric acid
- CuSO4+ NaOH+Tartaric acid
- AgNO3+NH4OH
- K2Cr2O7+Cone.H2SO4
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Question#27:Acetaldehyde reacts normally with:
- Electrophiles only
- Nucleophiles only
- Electrophiles and nucleophiles
- Free radicals only
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Question#28: The structural formula of the compound which is an isomer of acetone is:
- CH3 CH2 CHO
- CH3 CH2 CH2CHO
- CH3 CH2OH
- CH3 CH2 CH2OH
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Question#29:2-Pentanone and 3-pentanone are:
- Metamers
- Functional group isomers
- Geometrical isomers
- Chain isomers
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Question#30: Ethylene is oxidized to acetaldehyde on a commercial scale by the use of the catalyst which is:
- PdCI2 and CuCI2
- FeO and Mo2O3
- Na2Cr2O7 and H2SO4
- All of these
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