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This section includes 11242 Mcqs, each offering curated multiple-choice questions to sharpen your Joint Entrance Exam - Main (JEE Main) knowledge and support exam preparation. Choose a topic below to get started.
| 2101. |
On prolonged heating of ammonium cyanate or urea, we get [DPMT 1982; CPMT 1979; MP PMT 1996] |
| A. | \[{{N}_{2}}\] |
| B. | \[C{{O}_{2}}\] |
| C. | Biurette |
| D. | Ammonium carbonate |
| Answer» D. Ammonium carbonate | |
| 2102. |
Which of the following is the strongest acid [NCERT 1984] |
| A. | \[C{{H}_{3}}COOH\] |
| B. | \[BrC{{H}_{2}}COOH\] |
| C. | \[ClC{{H}_{2}}COOH\] |
| D. | \[FC{{H}_{2}}COOH\] |
| Answer» E. | |
| 2103. |
Hydrolysis of an ester gives a carboxylic acid which on Kolbe's electrolysis yields ethane. The ester is [EAMCET 1997; Manipal PMT 2001] |
| A. | Ethyl methonoate |
| B. | Methyl ethanoate |
| C. | Propylamine |
| D. | Ethylamine |
| Answer» C. Propylamine | |
| 2104. |
When propanamide reacts with \[B{{r}_{2}}\] and \[NaOH\] then which of the following compound is formed [Manipal 2001] |
| A. | Ethyl alcohol |
| B. | Propyl alcohol |
| C. | Propyl amine |
| D. | Ethylamine |
| Answer» E. | |
| 2105. |
If the enolate ion combines with carbonyl group of ester, we get [DPMT 2005] |
| A. | Aldol |
| B. | \[\alpha ,\,\beta \]-unsaturated ester |
| C. | \[\beta \]-keto aldehyde |
| D. | Acid |
| Answer» D. Acid | |
| 2106. |
Which of the following compounds will react with \[NaHC{{O}_{3}}\] solution to give sodium salt and carbon dioxide [DPMT 2005] |
| A. | Acetic acid |
| B. | \[n\]-hexanol |
| C. | Phenol |
| D. | Both A and C |
| Answer» B. \[n\]-hexanol | |
| 2107. |
A carboxylic acid is converted into its anhydride using [J & K 2005] |
| A. | Thionyl chloride |
| B. | Sulphur chloride |
| C. | Sulphuric acid |
| D. | Phosphorus pent oxide |
| Answer» E. | |
| 2108. |
Order of hydrolysis for the following (I) \[RCOCl\] (II) \[RCOOR\] (III) \[RCON{{H}_{2}}\] (IV) \[{{(RCO)}_{2}}O\] [DPMT 2005] |
| A. | I>IV>II>III |
| B. | I>II>III>IV |
| C. | I>III>II>IV |
| D. | IV>III>II>I |
| Answer» B. I>II>III>IV | |
| 2109. |
Colouration of \[B{{r}_{2}}/CC{{l}_{4}}\] will be discharged by [Orissa JEE 2005] |
| A. | Cinnamic acid |
| B. | Benzoic acid |
| C. | o-phthalic acid |
| D. | Acetophenone |
| Answer» B. Benzoic acid | |
| 2110. |
Which of the following is an amphoteric acid [KCET 2005] |
| A. | Glycine |
| B. | Salicylic acid |
| C. | Benzoic acid |
| D. | Citric acid |
| Answer» B. Salicylic acid | |
| 2111. |
Which class of compounds shows H-bonding even more than in alcohols |
| A. | Phenols |
| B. | Carboxylic acids |
| C. | Ethers |
| D. | Aldehydes |
| Answer» C. Ethers | |
| 2112. |
X is heated with soda lime and gives ethane. X is [AFMC 2005] |
| A. | Ethanoic acid |
| B. | Methanoic acid |
| C. | Propanoic acid |
| D. | Either A or C |
| Answer» D. Either A or C | |
| 2113. |
Among the following acids which has the lowest \[pKa\] value [AIEEE 2005] |
| A. | \[C{{H}_{3}}COOH\] |
| B. | \[HCOOH\] |
| C. | \[{{(C{{H}_{3}})}_{2}}CH-COOH\] |
| D. | \[C{{H}_{3}}C{{H}_{2}}COOH\] |
| Answer» C. \[{{(C{{H}_{3}})}_{2}}CH-COOH\] | |
| 2114. |
\[{{C}_{6}}{{H}_{5}}CONHC{{H}_{3}}\] can be converted into \[{{C}_{6}}{{H}_{5}}C{{H}_{2}}NHC{{H}_{3}}\] by [AIIMS 2005] |
| A. | \[NaB{{H}_{4}}\] |
| B. | \[{{H}_{2}}-Pd/C\] |
| C. | \[LiAl{{H}_{4}}\] |
| D. | \[Zn-Hg/HCl\] |
| Answer» E. | |
| 2115. |
What happens when 2-hydroxy benzoic acid is distilled with zinc dust, it gives [MP PET/PMT 1998] |
| A. | Phenol |
| B. | Benzoic acid |
| C. | Benzaldehyde |
| D. | A polymeric compound |
| Answer» C. Benzaldehyde | |
| 2116. |
\[C{{H}_{3}}C{{O}_{2}}{{C}_{2}}{{H}_{5}}\] on reaction with sodium ethoxide in ethanol gives A, which on heating in the presence of acid gives B compound B is [AIIMS 2005] |
| A. | \[C{{H}_{3}}COC{{H}_{2}}COOH\] |
| B. | \[C{{H}_{3}}COC{{H}_{3}}\] |
| C. | |
| D. | \[C{{H}_{2}}=C\ <\begin{matrix} O{{C}_{2}}{{H}_{5}} \\ O{{C}_{2}}{{H}_{5}} \\ \end{matrix}\] |
| Answer» D. \[C{{H}_{2}}=C\ <\begin{matrix} O{{C}_{2}}{{H}_{5}} \\ O{{C}_{2}}{{H}_{5}} \\ \end{matrix}\] | |
| 2117. |
In a set reactions acid yielded a product D \[C{{H}_{3}}COOH\xrightarrow{SOC{{l}_{2}}}A\underset{Anhr.\,AlC{{l}_{3}}}{\mathop{\xrightarrow{Benzene}}}\,B\xrightarrow{HCN}C\xrightarrow{HOH}D.\] [CBSE PMT 2005] |
| A. | |
| B. | |
| C. | |
| D. | |
| Answer» B. | |
| 2118. |
4-methyl benzene sulphonic acid reacts with sodium acetate to give [IIT-JEE (Screening) 2005] |
| A. | |
| B. | |
| C. | |
| D. | |
| Answer» B. | |
| 2119. |
Lactic acid molecule has [MH CET 2004] |
| A. | One chiral carbon atom |
| B. | Two chiral carbon atoms |
| C. | No chiral carbon atom |
| D. | As asymetric molecule |
| Answer» B. Two chiral carbon atoms | |
| 2120. |
Fruity smell is given by [MH CET 2004] |
| A. | Esters |
| B. | Alcohols |
| C. | Chloroform |
| D. | Acid anhydrides |
| Answer» B. Alcohols | |
| 2121. |
When \[C{{H}_{3}}COOH\] reacts with \[C{{H}_{3}}-Mg-X\] [BVP 2003] |
| A. | \[C{{H}_{3}}COX\]is formed |
| B. | Hydrocarbon is formed |
| C. | Acetone is formed |
| D. | Alcohol is formed |
| Answer» C. Acetone is formed | |
| 2122. |
\[C{{H}_{3}}CHO\xrightarrow{HCN}A\xrightarrow{HOH}B.\] The product B is [Pb. CET 2003] |
| A. | Malonic acid |
| B. | Glycolic acid |
| C. | Lactic acid |
| D. | Malic acid |
| Answer» D. Malic acid | |
| 2123. |
Urea upon hydrolysis yields [Pb. CET 2001] |
| A. | Acetamide |
| B. | Carbonic acid |
| C. | Ammonium hydroxide |
| D. | \[N{{O}_{2}}\] |
| Answer» C. Ammonium hydroxide | |
| 2124. |
Acetic acid reacts with \[PC{{l}_{5}}\]to form [Pb. CET 2001] |
| A. | \[C{{H}_{3}}COCl\] |
| B. | \[CHC{{l}_{2}}COOH\] |
| C. | \[C{{H}_{2}}ClCOOH\] |
| D. | \[C{{H}_{3}}COOCl\] |
| Answer» B. \[CHC{{l}_{2}}COOH\] | |
| 2125. |
Benedict's solution is not reduced by [CPMT 2004] |
| A. | Formaldehyde |
| B. | Acetaldehyde |
| C. | Glucose |
| D. | Acetic anhydride |
| Answer» E. | |
| 2126. |
\[C{{H}_{3}}COOH\] is reacted with \[CH\equiv CH\] in presence of \[H{{g}^{++}},\] the product is [DPMT 2004; BHU 1998] |
| A. | \[\underset{\underset{C{{H}_{2}}(OOC{{H}_{3}})\,\,\,\,}{\mathop{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}}\,}{\mathop{C{{H}_{3}}(OOCC{{H}_{3}})}}\,\] |
| B. | \[\underset{\begin{smallmatrix} \,\,| \\ C{{H}_{2}}-(OOC-C{{H}_{3}})\,\, \end{smallmatrix}}{\mathop{C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}}\,\] |
| C. | \[\underset{\begin{smallmatrix} \,\,| \\ CH{{(OOC-C{{H}_{3}})}_{2}} \end{smallmatrix}}{\mathop{C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}}\,\] |
| D. | None of these |
| Answer» D. None of these | |
| 2127. |
Which of the following is most acidic [MP PET 2004] |
| A. | Picric acid |
| B. | p-nitrophenol |
| C. | m-nitrophenol |
| D. | o-p dinitrophenol |
| Answer» B. p-nitrophenol | |
| 2128. |
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 [KCET 2004] |
| A. | Ethyl benzoate |
| B. | Ethyl formate |
| C. | Ethyl acetate |
| D. | Methyl acetate |
| Answer» B. Ethyl formate | |
| 2129. |
The reagent which does not give acid chloride on treating with a carboxylic acid is [KCET 2004] |
| A. | \[PC{{l}_{5}}\] |
| B. | \[C{{l}_{2}}\] |
| C. | \[SOC{{l}_{2}}\] |
| D. | \[PC{{l}_{3}}\] |
| Answer» C. \[SOC{{l}_{2}}\] | |
| 2130. |
When anisole is heated with HI, the product is [CET Pune 1998] |
| A. | Phenyl iodide and methyl iodide |
| B. | Phenol and methanol |
| C. | Phenyl iodide and methanol |
| D. | Methyl iodide and phenol |
| Answer» E. | |
| 2131. |
The reaction of an ester \[RCOO{R}'\] with an alcohol \[{R}''OH\] in the presence of an acid gives [Kerala PMT 2004] |
| A. | \[RCOOH\] |
| B. | \[{R}'COOH\] |
| C. | \[{R}''COOR\] |
| D. | \[RCOO{R}''\] |
| E. | \[{R}'COO{R}''\] |
| Answer» E. \[{R}'COO{R}''\] | |
| 2132. |
o-Toluic acid on reaction with \[B{{r}_{2}}+Fe,\]gives [AIIMS 2004] |
| A. | |
| B. | |
| C. | |
| D. | |
| Answer» D. | |
| 2133. |
On mixing ethyl acetate with aqueous sodium chloride, the composition of the resultant solution is [AIEEE 2004] |
| A. | \[C{{H}_{3}}COCl+{{C}_{2}}{{H}_{5}}OH+NaOH\] |
| B. | \[C{{H}_{3}}COONa+{{C}_{2}}{{H}_{5}}OH\] |
| C. | \[C{{H}_{3}}COO{{C}_{2}}{{H}_{5}}+NaCl\] |
| D. | \[C{{H}_{3}}Cl+{{C}_{2}}{{H}_{5}}COONa\] |
| Answer» D. \[C{{H}_{3}}Cl+{{C}_{2}}{{H}_{5}}COONa\] | |
| 2134. |
Consider the acidity of the carboxylic acids \[PhCOOH\] \[o-N{{O}_{2}}{{C}_{6}}{{H}_{4}}COOH\] \[p-N{{O}_{2}}{{C}_{6}}{{H}_{4}}COOH\] \[m-N{{O}_{2}}{{C}_{6}}{{H}_{4}}COOH\] Which of the following order is correct? [AIEEE 2004] |
| A. | \[b>d>a>c\] |
| B. | \[b>d>c>a\] |
| C. | \[a>b>c>d\] |
| D. | \[b>c>d>a\] |
| Answer» E. | |
| 2135. |
Which of the following is the correct order of increasing strengths of carboxylic acids |
| A. | \[C{{H}_{2}}FCOOH<C{{H}_{3}}COOH\]\[<C{{H}_{2}}ClCOOH<CC{{l}_{3}}COOH\] |
| B. | \[C{{H}_{3}}COOH<C{{H}_{2}}ClCOOH\]\[<C{{H}_{2}}FCOOH<CC{{l}_{3}}COOH\] |
| C. | \[C{{H}_{2}}ClCOOH<C{{H}_{2}}FCOOH\]\[<CC{{l}_{3}}COOH<C{{H}_{3}}COOH\] |
| D. | \[CC{{l}_{3}}COOH<C{{H}_{2}}ClCOOH\]\[<C{{H}_{2}}FCOOH<C{{H}_{3}}COOH\] |
| Answer» C. \[C{{H}_{2}}ClCOOH<C{{H}_{2}}FCOOH\]\[<CC{{l}_{3}}COOH<C{{H}_{3}}COOH\] | |
| 2136. |
Treatment of benzoic acid with \[C{{l}_{2}}/FeC{{l}_{3}}\] will give [KCET 1998; CET Pune 1998] |
| A. | p-chlorobenzoic acid |
| B. | o-chlorobenzoic acid |
| C. | 2, 4-dichlorobenzoic acid |
| D. | m-chlorobenzoic aicd |
| Answer» E. | |
| 2137. |
Acetic anhydride reacts with diethyl ether in presence of anhydrous \[AlC{{l}_{3}}\] to form [MP PMT 1992] |
| A. | Ethyl acetate |
| B. | Methyl propionate |
| C. | Methyl acetate |
| D. | Propionic acid |
| Answer» B. Methyl propionate | |
| 2138. |
What will happen if \[LiAl{{H}_{4}}\] is added to an ester [CBSE PMT 2000] |
| A. | Two units of alcohol are obtained |
| B. | One unit of alcohol and one unit of acid is obtained |
| C. | Two units of acids are obtained |
| D. | None of these |
| Answer» B. One unit of alcohol and one unit of acid is obtained | |
| 2139. |
Silver benzoate reacts with bromine to form [KCET 1996] |
| A. | |
| B. | |
| C. | |
| D. | |
| Answer» E. | |
| 2140. |
Lactic acid on heating with conc. \[{{H}_{2}}S{{O}_{4}}\] gives [MP PET 1996] |
| A. | Acetic acid |
| B. | Propionic acid |
| C. | Acrylic acid |
| D. | Formic acid |
| Answer» D. Formic acid | |
| 2141. |
Acetamide is [MP PET 1990; RPMT 1999] |
| A. | Acidic |
| B. | Basic |
| C. | Neutral |
| D. | Amphoteric |
| Answer» E. | |
| 2142. |
Oxalic acid on being heated upto \[{{90}^{o}}C\] with conc. \[{{H}_{2}}S{{O}_{4}}\] forms [AFMC 1989; MP PET 1994; MP PMT 1989] |
| A. | \[HCOOH+C{{O}_{2}}\] |
| B. | \[C{{O}_{2}}+{{H}_{2}}O\] |
| C. | \[C{{O}_{2}}+CO+{{H}_{2}}O\] |
| D. | \[HCOOH+CO\] |
| Answer» D. \[HCOOH+CO\] | |
| 2143. |
When benzoic acid is treated with \[PC{{l}_{5}}\]at 100°C, it gives [Orissa JEE 2003] |
| A. | Benzoyl chloride |
| B. | o-chlorobenzoic acid |
| C. | p-chlorobenzoic acid |
| D. | Benzyl chloride |
| Answer» B. o-chlorobenzoic acid | |
| 2144. |
The reagent used for converting ethanoic acid to ethanol is [KCET 1996; EAMCET 1998] |
| A. | \[LiAl{{H}_{4}}\] |
| B. | \[KMn{{O}_{4}}\] |
| C. | \[PC{{l}_{3}}\] |
| D. | \[{{K}_{2}}C{{r}_{2}}{{O}_{7}}/{{H}^{+}}\] |
| Answer» B. \[KMn{{O}_{4}}\] | |
| 2145. |
Nitration of benzoic acid gives [MP PMT 1997] |
| A. | 3-nitrobenzoic acid |
| B. | 2-nitrobenzoic acid |
| C. | 2, 3-dinitrobenzoic acid |
| D. | 2, 4-dinitrobenzoic acid |
| Answer» B. 2-nitrobenzoic acid | |
| 2146. |
The above shown polymer is obtained when a carbon compound is allowed to stand. It is a white solid. The polymer is [CBSE PMT 1989] |
| A. | Trioxane |
| B. | Formose |
| C. | Paraformaldehyde |
| D. | Metaldehyde |
| Answer» B. Formose | |
| 2147. |
An aqueous solution of urea [CPMT 1983] |
| A. | Is neutral |
| B. | Is acidic |
| C. | Is basic |
| D. | Can act as an acid and a base |
| Answer» B. Is acidic | |
| 2148. |
Which of the following acids has the smallest dissociation constant [IIT-JEE (Screening) 2002] |
| A. | \[C{{H}_{3}}CHFCOOH\] |
| B. | \[FC{{H}_{2}}C{{H}_{2}}COOH\] |
| C. | \[BrC{{H}_{2}}C{{H}_{2}}COOH\] |
| D. | \[C{{H}_{3}}CHBrCOOH\] |
| Answer» D. \[C{{H}_{3}}CHBrCOOH\] | |
| 2149. |
When glycerol is heated with \[KHS{{O}_{4}}\] it gives [CPMT 1974, 85; MP PMT 1988, 90, 91, 92, 94; MP PET 1988, 92] |
| A. | \[C{{H}_{2}}=CH-C{{H}_{3}}\] |
| B. | \[C{{H}_{2}}=CH-C{{H}_{2}}OH\] |
| C. | \[C{{H}_{2}}=CH-CHO\] |
| D. | \[C{{H}_{2}}=C=C{{H}_{2}}\] |
| Answer» D. \[C{{H}_{2}}=C=C{{H}_{2}}\] | |
| 2150. |
Because of resonance the oxygen atom of \[-OH\] group of phenol |
| A. | Acquires positive charge |
| B. | Acquires negative charge |
| C. | Remains uneffected |
| D. | Liberates |
| Answer» B. Acquires negative charge | |