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JEE • CHEMISTRY • ALDEHYDES & KETONES & CARBOXYLIC ACIDS

Aldehydes & ketones & carboxylic acids practice · Mixed difficulty

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These sets use single-correct-answer MCQs. They do not cover every JEE Main or JEE Advanced question format and are not full-length mock papers.

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Showing 151-180 of 255 questions

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151 Medium
151 of 255
Analyzing +4 | -1
Among the following, the most acidic is
View answer and explanation
Correct option: C
Cl2CHCOOH\mathrm{C}{\mathrm{l}_2}\mathrm{CHCOOH}
Option C (Cl2CHCOOH) is correct because the presence of more electron-withdrawing chlorine atoms closer to the carboxylic acid group increases acidity.
152 Easy
152 of 255
Understanding +4 | -1
Benzaldehyde, when heated with concentrated KOH\mathrm{KOH} solution, gives:
View answer and explanation
Correct option: D
Mixture of C6H5COOK   and    C6H5CH2OH{\mathrm{C}_6}{\mathrm{H}_5}\mathrm{COOK}\,\mathrm{\;and\;}\,\,{\mathrm{C}_6}{\mathrm{H}_5}\mathrm{C}{\mathrm{H}_2}\mathrm{OH}
Option D is correct because benzaldehyde undergoes Cannizzaro reaction in the presence of concentrated KOH, yielding a mixture of potassium benzoate and benzyl alcohol.
153 Medium
153 of 255
Remembering +4 | -1
Acetone is used:
View answer and explanation
Correct option: D
All are correct
Option D (All are correct) is correct because acetone is used as a solvent, in nail polishes, and for storing acetylene under pressure.
154 Medium
154 of 255
Understanding +4 | -1
In which of the following reactions, both oxidized and reduced forms of the same compound are obtained?
View answer and explanation
Correct option: B
Cannizzaro reaction
Option B (Cannizzaro reaction) is correct because it involves the self-oxidation and reduction of an aldehyde without alpha-hydrogens.
155 Medium
155 of 255
Understanding +4 | -1
Identify A and B in the following reaction
CH3−CH3←BCH3COOH→ACH3CH2OH                                  A                                                      B\begin{array}{l} \mathrm{C}{\mathrm{H}_3} - \mathrm{C}{\mathrm{H}_3}\xleftarrow{B}\mathrm{C}{\mathrm{H}_3}\mathrm{COOH}\xrightarrow{A}\mathrm{C}{\mathrm{H}_3}\mathrm{C}{\mathrm{H}_2}\mathrm{OH}\\ \;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\mathrm{A}\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\;\mathrm{B} \end{array}
View answer and explanation
Correct option: C
LiAlH4HI+red  P\mathrm{LiAl}{\mathrm{H}_4}\mathrm{HI} + \mathrm{red}\;\mathrm{ P}
Option C (LiAlH4HI+red  P\mathrm{LiAl}{\mathrm{H}_4}\mathrm{HI} + \mathrm{red}\;\mathrm{ P}) is correct because LiAlH4LiAlH_4 reduces carboxylic acid to alcohol, and HI/red P reduces it to alkane.
156 Easy
156 of 255
Understanding +4 | -1
Reaction of a carbonyl compound with one of the following reagents involves nucleophilic addition followed by elimination of water. The reagent is:
View answer and explanation
Correct option: D
Hydrazine in presence of feebly acidic solution
Option D (Hydrazine in presence of feebly acidic solution) is correct because hydrazine reacts with carbonyl compounds via nucleophilic addition followed by water elimination to form hydrazones.
157 Medium
157 of 255
Analyzing +4 | -1
Through which of the following reactions number of carbon atoms can be increased in the chain?

(i) Grignard reaction

(ii) Cannizzaro's reaction

(iii) Aldol condensation

(iv) HVZ reaction

Choose the correct option.
View answer and explanation
Correct option: A
Only (iii) and (i)
Option A is correct because Grignard reaction and Aldol condensation are carbon-carbon bond forming reactions, thus increasing the number of carbon atoms in the chain.
158 Medium
158 of 255
Analyzing +4 | -1
Assertion (A): Benzaldehyde is more reactive than ethanal towards nucleophilic attack.

Reason (R): Both benzaldehyde and acetaldehyde have alpha hydrogens.
View answer and explanation
Correct option: D
Both (A) and (R) are false
Option D is correct. Benzaldehyde is less reactive than ethanal towards nucleophilic attack due to steric hindrance, and benzaldehyde does not have alpha hydrogens.
159 Medium
159 of 255
Remembering +4 | -1
Benzaldehyde can be prepared from benzene by passing vapours of ____ and ____ in its solution in presence of catalyst mixture of aluminium chloride and cuprous chloride. The reaction is known is _____
View answer and explanation
Correct option: B
CO,HCl{CO}, {HCl}, Gattermann-Koch reaction
Option B (CO,HCl{CO}, {HCl}, Gattermann-Koch reaction) is correct because the Gattermann-Koch reaction uses carbon monoxide and hydrochloric acid in the presence of a catalyst to convert benzene to benzaldehyde.
160 Medium
160 of 255
Remembering +4 | -1
Salol (phenyl salicylate ) is used as an:
View answer and explanation
Correct option: D
Intestinal antiseptic
Option D (Intestinal antiseptic) is correct because Salol (phenyl salicylate) is used as an intestinal antiseptic due to its ability to break down into salicylic acid and phenol in the intestines.
161 Medium
161 of 255
Analyzing +4 | -1
Statement I: Acetaldehyde cannot be prepared by the Rosenmund reduction.

Statement II: Formyl chloride is unstable at room temperature.
View answer and explanation
Correct option: D
Statement II is correct, Statement I is incorrect.
Statement II is correct, Statement I is incorrect because Rosenmund reduction cannot be used to prepare formaldehyde, not acetaldehyde, due to the instability of formyl chloride.
162 Medium
162 of 255
Understanding +4 | -1
Which of the following compound is least reactive towards hydrolysis?
View answer and explanation
Correct option: A
Acetamide
Option A (Acetamide) is correct because amides are generally less reactive towards hydrolysis compared to acid chlorides, anhydrides, and esters due to resonance stabilization.
163 Medium
163 of 255
Analyzing +4 | -1
2-pentanone and 3-petanone can be distinguished by
View answer and explanation
Correct option: C
Iodoform reaction
Option C (Iodoform reaction) is correct because 2-pentanone has a methyl ketone group (CH₃CO) that reacts with I₂/NaOH to give a positive iodoform test, while 3-pentanone does not.
164 Medium
164 of 255
Understanding +4 | -1
Which will not give acetamide (no heating) on reaction with ammonia?
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Correct option: A
Acetic acid
Option A (Acetic acid) is correct because acetic acid reacts with ammonia to form ammonium acetate, which requires heating to form acetamide.
165 Hard
165 of 255
Understanding +4 | -1
Benzaldehyde reacts with excess of anhydrous ethyl alcohol in the presence of HClHCl, gives:
View answer and explanation
Correct option: C
C6H5CH(OC2H5)2{C_6}{H_5}CH{\left( {O{C_2}{H_5}} \right)_2}
Option C (C6H5CH(OC2H5)2{C_6}{H_5}CH{\left( {O{C_2}{H_5}} \right)_2}) is correct because benzaldehyde reacts with excess ethanol in the presence of HCl to form an acetal.
166 Medium
166 of 255
Remembering +4 | -1
Rosenmund’s reduction is used for the preparation of
View answer and explanation
Correct option: B
Aldehyde
Option B (Aldehyde) is correct because Rosenmund's reduction is used for the preparation of aldehydes from acyl chlorides.
167 Medium
167 of 255
Understanding +4 | -1
The number of aldehyde isomers for C4H8O{C_4}{H_8}O will be
View answer and explanation
Correct option: C
2
Option C (2) is correct because there are two aldehyde isomers for C4H8O: butanal and 2-methylpropanal.
168 Medium
168 of 255
Remembering +4 | -1
The elimination of CO2\mathrm{C}{\mathrm{O}_2} from a carboxylic acid is known as:
View answer and explanation
Correct option: C
Decarboxylation
Option C (Decarboxylation) is correct because decarboxylation is the process of removing a carboxyl group (COOH) from a molecule, releasing carbon dioxide.
169 Medium
169 of 255
Analyzing +4 | -1
Formaldehyde and formic acid can be distinguished by:
View answer and explanation
Correct option: D
NaHCO3\mathrm{NaHC}{\mathrm{O}_3}
Option D (NaHCO3\mathrm{NaHC}{\mathrm{O}_3}) is correct because formic acid reacts with sodium bicarbonate to produce carbon dioxide gas, while formaldehyde does not.
170 Hard
170 of 255
Understanding +4 | -1
Chlorobenzene →XReaction      Phenol  →YReaction    \xrightarrow[X]{{\mathrm{Reaction\;\;}}}\mathrm{\;Phenol\;}\xrightarrow[Y]{{\mathrm{Reaction\;\;}}} Salicyladehyde X  and  YX\;and\;Y reactions are respectively……….
View answer and explanation
Correct option: C
Dow and Reimer-Tiemann
Option C is correct. Chlorobenzene is converted to phenol by Dow's process, and phenol is converted to salicylaldehyde by the Reimer-Tiemann reaction.
171 Medium
171 of 255
Application +4 | -1
0.759 g of a silver salt of a dibasic organic acid on ignition left 0.463 g metallic silver. The equivalent weight of acid is:
View answer and explanation
Correct option: A
70
Option A (70) is correct because the equivalent weight of the acid is calculated using the equivalent weights of the silver salt and silver.
172 Medium
172 of 255
Remembering +4 | -1
Ketones can be converted to alkanes directly on reaction with
View answer and explanation
Correct option: C
HI/P4/Δ{HI} / {P}_4 / \Delta
Option C (HI/P4/Δ{HI} / {P}_4 / \Delta) is correct because ketones can be directly converted to alkanes using HI and red phosphorus under heating conditions.
173 Medium
173 of 255
Analyzing +4 | -1
An organic compound is boiled with alcoholic potash. The product is cooled and acidified with HCl. A white solid separates out. The starting compound may be
View answer and explanation
Correct option: A
Ethyl benzoate
Option A (Ethyl benzoate) is correct because it undergoes saponification with alcoholic potash to form potassium benzoate, which upon acidification yields benzoic acid (a white solid).
174 Easy
174 of 255
Understanding +4 | -1
Ethane can be obtained from ethanal in one step by:
View answer and explanation
Correct option: B
Zn-Hg + conc. HCl
Option B (Zn-Hg + conc. HCl) is correct because Clemmensen reduction uses zinc amalgam and concentrated hydrochloric acid to reduce carbonyl groups (C=O) to methylene groups (CH2).
175 Medium
175 of 255
Understanding +4 | -1
Assertion (A): A bright silver mirror is produced during the warming of an aldehyde with freshly prepared ammoniacal silver nitrate solution.

Reason (R): A bright silver mirror is produced due to the formation of silver metal.
View answer and explanation
Correct option: A
Both A\mathrm{A} and R\mathrm{R} are correct; and R\mathrm{R} is the correct explanation of A\mathrm{A}.
The correct answer is Both A\mathrm{A} and R\mathrm{R} are correct; and R\mathrm{R} is the correct explanation of A\mathrm{A} because the formation of a silver mirror is due to the reduction of silver ions to silver metal by the aldehyde.
176 Medium
176 of 255
Analyzing +4 | -1
The most acidic of the following is
View answer and explanation
Correct option: A
ClCH2COOH\mathrm{ClC}{\mathrm{H}_2}\mathrm{COOH}
Option A (ClCH2COOH\mathrm{ClC}{\mathrm{H}_2}\mathrm{COOH}) is correct because the electron-withdrawing chlorine atom increases the acidity through the -I effect.
177 Medium
177 of 255
Application +4 | -1
Nitration of salicylic acid will give:
View answer and explanation
Correct option: A
2,4,6-trinitophenol
Option A (2,4,6-trinitrophenol) is correct because the -COOH group of salicylic acid is replaced during nitration, leading to the formation of picric acid (2,4,6-trinitrophenol).
178 Medium
178 of 255
Application +4 | -1
The products A and B are
(CH3)3C−CHO→ (ii) H+(i) con.NaOHA+B\left(\mathrm{CH}_3\right)_3 \mathrm{C}-\mathrm{CHO} \xrightarrow[\text { (ii) } \mathrm{H}^{+}]{\text {(i) } \mathrm{con.}{\mathrm{NaOH}}} \mathrm{A}+\mathrm{B}
View answer and explanation
Correct option: C
A=(CH3)3C−CH2−OH,B=(CH3)3C−COOH\mathrm{A}=\left(\mathrm{CH}_3\right)_3 \mathrm{C}-\mathrm{CH}_2-\mathrm{OH}, \mathrm{B}=\left(\mathrm{CH}_3\right)_3 \mathrm{C}-\mathrm{COOH}
Option C (A=(CH3)3C-CH2-OH, B=(CH3)3C-COOH) is correct because the reaction is a Cannizzaro reaction, which produces an alcohol and a carboxylic acid.
179 Easy
179 of 255
Remembering +4 | -1
Acetophenone is used in:
View answer and explanation
Correct option: C
Perfumery
Option C (Perfumery) is correct because acetophenone has a pleasant odor and is commonly used as a fragrance component in perfumes.
180 Easy
180 of 255
Understanding +4 | -1
The reaction of acetaldehyde with Tollen’s reagent gives
View answer and explanation
Correct option: D
Acetic acid
Option D (Acetic acid) is correct because acetaldehyde is oxidized to acetic acid when it reacts with Tollen's reagent, which is a mild oxidizing agent.
Revision notes and key takeaways

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