Please refer to the MCQ Questions for Class 12 Chemistry Chapter 12 Aldehydes, Ketones and Carboxylic Acids with Answers. The following Aldehydes, Ketones and Carboxylic Acids Class 12 Chemistry MCQ Questions have been designed based on the latest syllabus and examination pattern for Class 12. Our experts have designed MCQ Questions for Class 12 Chemistry with Answers for all chapters in your NCERT Class 12 Chemistry book.
Aldehydes, Ketones and Carboxylic Acids Class 12 MCQ Questions with Answers
See below Aldehydes, Ketones and Carboxylic Acids Class 12 Chemistry MCQ Questions, solve the questions and compare your answers with the solutions provided below.
Question. The –OH group of an alcohol or the – COOH group
of a carboxylic acid can be replaced by – Cl using
(a) phosphorus pentachloride
(b) hypochlorous acid
(c) chlorine
(d) hydrochloric acid.
Answer
A
Question. Which one of the following orders of acid strength is correct?
(a) RCOOH > ROH > HOH > HC≡CH
(b) RCOOH > HOH > ROH > HC≡ CH
(c) RCOOH > HOH > HC≡ CH > ROH
(d) RCOOH > HC≡ CH > HOH > ROH
Answer
B
Question. Ethyl benzoate can be prepared from benzoic acid by using
(a) ethyl alcohol
(b) ethyl alcohol and dry HCl
(c) ethyl chloride
(d) sodium ethoxide.
Answer
B
Question. Reduction by LiAlH4 of hydrolysed product of an ester gives
(a) two alcohols
(b) two aldehydes
(c) one acid and one alcohol
(d) two acids.
Answer
A
Question. Which one of the following compounds will react with NaHCO3 solution to give sodium salt and carbon dioxide?
(a) Acetic acid
(b) n-Hexanol
(c) Phenol
(d) Both (b) and (c)
Answer
A
Question. An acyl halide is formed when PCl5 reacts with an
(a) amide
(b) ester
(c) acid
(d) alcohol.
Answer
c
Question. Benzoic acid gives benzene on being heated with X and phenol gives benzene on being heated with Y. Therefore, X and Y are respectively
(a) soda-lime and copper
(b) Zn dust and NaOH
(c) Zn dust and soda-lime
(d) soda-lime and zinc dust.
Answer
D
Question. A is a lighter phenol and B is an aromatic carboxylic acid. Separation of a mixture of A and B can be carried out easily by using a solution of
(a) sodium hydroxide
(b) sodium sulphate
(c) calcium chloride
(d) sodium bicarbonate.
Answer
D
Question. The compound formed when malonic acid is heated with urea is
(a) cinnamic acid
(b) butyric acid
(c) barbituric acid
(d) crotonic acid.
Answer
C
Question. Among the following the strongest acid is
(a) CH3COOH
(b) CH2ClCH2COOH
(c) CH2ClCOOH
(d) CH3CH2COOH
Answer
C
Question. Which of the following is the correct decreasing order of acidic strength of (i) methanoic acid (ii) ethanoic acid (iii) propanoic acid (iv) butanoic acid
(a) (i) > (ii) > (iii) > (iv)
(b) (ii) > (iii) > (iv) > (i)
(c) (i) > (iv) > (iii) > (ii)
(d) (iv) > (i) > (iii) > (ii)
Answer
A
Question. Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is
(a) CH3COOCH3
(b) CH3CONH2
(c) CH3COOCOCH3
(d) CH3COCl
Answer
D
Question. The relative reactivities of acyl compounds towards nucleophilic substitution are in the order of
(a) acid anhydride > amide > ester > acyl chloride
(b) acyl chloride > ester > acid anhydride > amide
(c) acyl chloride > acid anhydride > ester > amide
(d) ester > acyl chloride > amide > acid anhydride.
Answer
C
Question. Benzoic acid gives benzene on being heated with X and phenol gives benzene on being heated with Y. Therefore, X and Y are respectively
(a) soda-lime and copper
(b) Zn dust and NaOH
(c) Zn dust and soda-lime
(d) soda-lime and zinc dust.
Answer
D
Question. Consider the acidity of the carboxylic acids
I. PhCOOH
II. o-NO2C6H4COOH
III. p-NO2C6H4COOH
IV. m-NO2C6H4COOH
Which of the following order is correct?
(a) I > II > III > IV
(b) II > IV > III > I
(c) Il > IV > I > III
(d) II > III> IV > I
Answer
D
Question. Which of the following is a better reducing agent for the following reduction?
RCOOH → RCH2OH
(a) SnCL2/HCl
(b) NaBH4 /ether
(c) H2 /Pd
(d) N2H4 / C2H5ONa
(e) B2H6 /ether
Answer
E
Question. Identify the organic compound which, on beating with strong solution of NaOH , partly converted into an, acid salt and partly into alcohol.
(a) Benzyl alcohol
(b) Acetaldehyde
(c) Acetone
(d) Benzaldehyde
Answer
D
Question. An important reaction of acetone is auto condensation in the presence of concentrated sulphuric acid to give the aromatic compund
(a) mesitylene
(b) mesityl oxide
(c) trioxan
(d) phorone
Answer
A
Question. End product of the following reaction is


Answer
C
Question. Which of the following represents the correct order of the activity in the given compounds?
(a) CH3COOH> BrCH2COOH> CICH2COOH
>FCH2COOH
(b) FCH2COOH> CH3COOH> BrCH2COOH
> CICH2COOH
(c) BrCHH2COOH> CICH2COOH> FCH2COOH
>CH3COOH
(d) FCH2COOH> CICH2COOH> BrCH2COOH
>CH3COOH
Answer
D
Question.

Answer
C
Question. In the reaction sequence,
A →CH3CH2MgBr B →H3O⊕ →C5H12O compound A is
(a) 1-propanol
(b) propanol-3
(c) ethanal
(d) 2-propanol
Answer
B
Question. Tollen’s reagent is
(a) [Ag(NH3)2 ]NO3
(b) [Ag(NH3)2 ]Br
(c) Both (a) and (b)
(d) None of these
Answer
A
Question. A compound A has a molecular fommla C2Cl3OH. It reduces Fehling’s solution and on oxidation, gives a monocarboxylic acidB. A can be obtained by the action of chlorine on ethyl alcohol. A is
(a) chloroform
(b) chloral
(c) methyl chloride
(d) monochloroacetic acid
Answer
B
Question. An organic compound A upon reacting with NH3 gives B. On heating, B gives C. C in the presence of KOH reacts with Br2 to give CH3CH2NH2 . A is
(a) CH3COOH
(b) CH3CH2CH2COOH
(c) CH3—CH—COOH
l
CH3
(d) CH3CH2COOH
Answer
D
Question. The acetophenone can be converted to etbylbenzene by reaction with
(a) LiAIH4
(b) H2NOH
(c) Pd / BaSO4-H2
(d) Zn-Hg / HCI
Answer
D
Question. The correct order of acidic strengths of the carboxylic acids is
(a) formic acid < benzoic acid < acetic acid
(b) formic acid < acetic acid < benzoic acid
(c) acetic acid < formic acid < benzoic acid
(d) acetic acid < benzoic acid < formic acid
Answer
D
Question. The compound K is

Answer
C
Question. Which of the following reagent is used to distinguish between methanoic acid and ethanoic acid
(a) Tollen’s reagent
(b) FeCl3 solution
(c) NaOH solution
(d) Na2CO3 solution
Answer
A
Question. 3-hydroxybutanal is formed when (X) reacts with (Y) in dilute ( Z) solution. What are X, Y and Z?
X Y Z
(a) CH3CHO, (CH3)2CO, NaOH
(b) CH3CHO, CH3CHO, NaCl
(c) (CH3)2CO, (CH3)2 CO, HCl
(d) CH3CHO, CH3CHO, NaOH
Answer
D
Question. Oxidation of which compound is not possible?
(a) CH3—COOH
(b) CH3—CO—CH3
(c) CH3—CHO
(d) CH3—CH2—OH
Answer
A
Question. Carboxylic acids readily dissolve in aqueous sodium bicarbonate, liberating carbon dioxide. Which one of the following is correct?
(a) Free carboxylic acid and its conjugate base are of comparable stability
(b) The free carboxylic acid is more stable than its conjugate base
(c) The conjugate base of the carboxylic acid is more stable than the free carboxylic acid
(d) The conjugate acid of the carboxylic acid is more stable than the free carboxylic acid
Answer
C
Question. Which of the following acid reduces Tollen’ reagent?
(a) Formic acid
(b) Acetic acid
(c) Lactic acid
(d) Oxalic acid
Answer
A
Question. What will be the end product (B) in the following sequence of reactions?

(a) 1, 2-dibromobenzene
(b) 1, 2-dibromobenzaldehyde
(c) 1, 3-dibromobenzene
(d) 1, 4-dibromobenzene
Answer
C
Question. The compound that does not liberate CO2 on treatment with aqueous sodium bicarbonate solution is
(a) benzoic acid
(b) benzenesulphonic acid
(c) salicylic acid
(d) carbolic acid (Phenol)
Answer
D
Question. The gas evolved on heating alkali formate with sodaiime is
(a) CO
(b) CO2
(c) hydrogen
(d) water vapour
Answer
C
Question.

Answer
A
Question. In the reaction, R—X →Alcoholic KCN A →Dilute HCI B The product B is
(a) alkyl chloride
(b) aldehyde
(c) carboxylic acid
(d) ketone
Answer
C
Question. The reaction, RCOOH + N3H →Conc.II2SO4
RNH2 + CO2 + N2 is called
(a) Lossen reaction
(c) Curtius reaction
(b) Schmidt reaction
(d) Ullmann reaction
Answer
B
Question. Which of the following acids has the smallest dissociation constant ?
(a) CH3CHFCOOH
(b) FCH2CH2COOH
(c) BrCH2CH2 COOH
(d) CH3CHBrCOOH
Answer
C
Question. A is a lighter phenol and B is an aromatic carboxylic acid. Separation of a mixture of A and B can be carried out easily by using a solution of
(a) sodium hydroxide
(b) sodium sulphate
(c) calcium chloride
(d) sodium bicarbonate.
Answer
D
Question. The compound formed when malonic acid is heated with urea is
(a) cinnamic acid
(b) butyric acid
(c) barbituric acid
(d) crotonic acid.
Answer
C
Question. Among the following the strongest acid is
(a) CH3COOH
(b) CH2ClCH2COOH
(c) CH2ClCOOH
(d) CH3CH2COOH
Answer
C
Question. Which of the following is the correct decreasing order of acidic strength of (i) methanoic acid (ii) ethanoic acid (iii) propanoic acid (iv) butanoic acid
(a) (i) > (ii) > (iii) > (iv)
(b) (ii) > (iii) > (iv) > (i)
(c) (i) > (iv) > (iii) > (ii)
(d) (iv) > (i) > (iii) > (ii)
Answer
A
Question. Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is
(a) CH3COOCH3
(b) CH3CONH2
(c) CH3COOCOCH3
(d) CH3COCl
Answer
D
Question. The relative reactivities of acyl compounds towards nucleophilic substitution are in the order of
(a) acid anhydride > amide > ester > acyl chloride
(b) acyl chloride > ester > acid anhydride > amide
(c) acyl chloride > acid anhydride > ester > amide
(d) ester > acyl chloride > amide > acid anhydride.
Answer
C
Question. Benzoic acid gives benzene on being heated with X and phenol gives benzene on being heated with Y. Therefore, X and Y are respectively
(a) soda-lime and copper
(b) Zn dust and NaOH
(c) Zn dust and soda-lime
(d) soda-lime and zinc dust.
Answer
D
Question. A is a lighter phenol and B is an aromatic carboxylic acid. Separation of a mixture of A and B can be carried out easily by using a solution of
(a) sodium hydroxide
(b) sodium sulphate
(c) calcium chloride
(d) sodium bicarbonate.
Answer
D
Question. The compound formed when malonic acid is heated with urea is
(a) cinnamic acid
(b) butyric acid
(c) barbituric acid
(d) crotonic acid.
Answer
C
Question. Among the following the strongest acid is
(a) CH3COOH
(b) CH2ClCH2COOH
(c) CH2ClCOOH
(d) CH3CH2COOH
Answer
C
Question. Which of the following is the correct decreasing order of acidic strength of (i) methanoic acid (ii) ethanoic acid (iii) propanoic acid (iv) butanoic acid
(a) (i) > (ii) > (iii) > (iv)
(b) (ii) > (iii) > (iv) > (i)
(c) (i) > (iv) > (iii) > (ii)
(d) (iv) > (i) > (iii) > (ii)
Answer
A
Question. Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is
(a) CH3COOCH3
(b) CH3CONH2
(c) CH3COOCOCH3
(d) CH3COCl
Answer
D
Question. The relative reactivities of acyl compounds towards nucleophilic substitution are in the order of
(a) acid anhydride > amide > ester > acyl chloride
(b) acyl chloride > ester > acid anhydride > amide
(c) acyl chloride > acid anhydride > ester > amide
(d) ester > acyl chloride > amide > acid anhydride.
Answer
C
Question. Self condensation of two moles of ethyl acetate in presence of sodium ethoxide yields
(a) ethyl propionate
(b) ethyl butyrate
(c) acetoacetic ester
(d) methyl acetoacetate
Answer
C
Question. Which one of the following esters cannot undergo Claisen self-condensation?
(a) C6H5CH2COOC2H5
(b) C6H5COOC2H5
(c) CH3CH2CH2CH2COOC2H5
(d) C6H11CH2COOC2H5
Answer
B
Question. Sodium formate on heating yields
(a) oxalic acid and H2
(b) sodium oxalate and H2
(c) CO2 and NaOH
(d) sodium oxalate.
Answer
B
