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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.
1801. |
The compound A with following sequence of reaction gave benzoic acid \[A\xrightarrow{NaN{{O}_{2}}/HCl}B\xrightarrow{KCN}C\xrightarrow{{{H}_{3}}{{O}^{+}}}\] benzoic acid. The compound A is [AMU 2001] |
A. | Nitrobenzene |
B. | Aniline |
C. | Benzaldehyde |
D. | Amides |
Answer» C. Benzaldehyde | |
1802. |
Which of the following chemicals are used to manufacture methyl isocyanate that caused ?Bhopal Tragedy? (i) Methylamine (ii) Phosgene (iii) Phosphine (iv) Dimethylamine [AIIMS 2005] |
A. | (i) and (iii) |
B. | (iii) and (iv) |
C. | (i) and (ii) |
D. | (ii) and (iv) |
Answer» D. (ii) and (iv) | |
1803. |
Alkyl cyanides when react with Grignard reagent, the product on hydrolysis found, is [MP PMT 1980] |
A. | Aldehyde |
B. | Ketone |
C. | Alcohol |
D. | Acid |
Answer» C. Alcohol | |
1804. |
Nitrobenzene on further excessive nitration gives [AFMC 2001] |
A. | Trinitrobenzene |
B. | m-dinitrobenzene |
C. | p-dinitrobenzene |
D. | All of these |
Answer» C. p-dinitrobenzene | |
1805. |
Among the following, the strongest base is [UPSEAT 2000; IIT-JEE (Screening) 2000] |
A. | \[{{C}_{6}}{{H}_{5}}N{{H}_{2}}\] |
B. | \[p-N{{O}_{2}}{{C}_{6}}{{H}_{4}}N{{H}_{2}}\] |
C. | \[m-N{{O}_{2}}-{{C}_{6}}{{H}_{4}}N{{H}_{2}}\] |
D. | \[{{C}_{6}}{{H}_{5}}C{{H}_{2}}N{{H}_{2}}\] |
Answer» E. | |
1806. |
Aniline and methyl amine can be differentiated by [DPMT 2000] |
A. | Reaction with chloroform and aqueous solution of KOH |
B. | Diazotisation followed by coupling with phenol |
C. | Reaction with \[HN{{O}_{2}}\] |
D. | None of these |
Answer» C. Reaction with \[HN{{O}_{2}}\] | |
1807. |
Decreasing order of basicity is [RPET 2000] (1) \[C{{H}_{3}}CON{{H}_{2}}\] (2) \[C{{H}_{3}}C{{H}_{2}}N{{H}_{2}}\] (3) Ph?\[C{{H}_{2}}CON{{H}_{2}}\] |
A. | 1 > 2 > 3 |
B. | 2 > 1 > 3 |
C. | 3 > 2 > 1 |
D. | None of these |
Answer» C. 3 > 2 > 1 | |
1808. |
\[RCOCl+2M{{e}_{2}}NH\to A+M{{e}_{2}}\overset{+\,\,\,\,\,\,\,\,\,\,\,\,\,\,}{\mathop{N{{H}_{2}}C{{l}^{-}}}}\,\]Here A is [RPET 2000] |
A. | |
B. | \[RCON{{H}_{2}}\] |
C. | \[RCONHMe\] |
D. | \[{{(RCO)}_{2}}NH\] |
Answer» B. \[RCON{{H}_{2}}\] | |
1809. |
\[C{{H}_{3}}CN\] is known as acetonitrile because [AMU 1999] |
A. | It contains an aceto group |
B. | On hydrolysis it gives acetic acid |
C. | Both A and B |
D. | None of these |
Answer» C. Both A and B | |
1810. |
In the reaction \[C{{H}_{3}}CN+C{{H}_{3}}MgI\to A\xrightarrow{{{H}_{2}}O/{{H}^{+}}}B\] The compound B is [KCET 1999] |
A. | Acetic acid |
B. | Acetone |
C. | Acetaldehyde |
D. | Ethyl alcohol |
Answer» C. Acetaldehyde | |
1811. |
Nitrosobenzene can be isolated from nitrobenzene under [DPMT 1982] |
A. | Metal and acid |
B. | Zn dust and \[N{{H}_{4}}Cl\] |
C. | Alkaline sodium arsenite |
D. | Cannot be isolated |
Answer» E. | |
1812. |
A primary amine can be converted to an alcohol by the action of [CET Pune 1998] |
A. | Alkali |
B. | Nitrous acid |
C. | Reducing agent |
D. | Oxidizing agent |
Answer» C. Reducing agent | |
1813. |
In the diazotisation of aniline with sodium nitrite and hydrochloric acid, an excess of hydrochloric acid is used primarily to [Pb. PMT 1998] |
A. | Suppress the concentration of free aniline available for coupling |
B. | Suppress hydrolysis of phenol |
C. | Insure a stoichiometric amount of nitrous acid |
D. | Neutralize the base liberated |
Answer» B. Suppress hydrolysis of phenol | |
1814. |
Which one is less alkaline [CPMT 1997] |
A. | |
B. | |
C. | |
D. | All of these |
Answer» B. | |
1815. |
The major product (70% to 80%) of the reaction between m-dinitrobenzene with \[N{{H}_{4}}HS\] is [AIIMS 1997] |
A. | |
B. | |
C. | |
D. | |
Answer» C. | |
1816. |
If methyl is alkyl group, then which order of basicity is correct [RPMT 1997] |
A. | \[{{R}_{2}}NH>RN{{H}_{2}}>{{R}_{3}}N>N{{H}_{3}}\] |
B. | \[{{R}_{2}}NH>{{R}_{3}}N>RN{{H}_{2}}>N{{H}_{3}}\] |
C. | \[RN{{H}_{2}}>N{{H}_{3}}>{{R}_{2}}NH>{{R}_{3}}N\] |
D. | \[N{{H}_{3}}>RN{{H}_{2}}>{{R}_{2}}NH>{{R}_{3}}N\] |
Answer» B. \[{{R}_{2}}NH>{{R}_{3}}N>RN{{H}_{2}}>N{{H}_{3}}\] | |
1817. |
p-Nitrobromobenzene can be converted to p-nitroaniline by using \[NaN{{H}_{2}}\]. The reaction proceeds through the intermediate named [Orissa JEE 2005] |
A. | Carbocation |
B. | Carbanion |
C. | Benzyne |
D. | Dianion |
Answer» D. Dianion | |
1818. |
Which one of the following is not a base [EAMCET 1997] |
A. | \[{{N}_{2}}{{H}_{4}}\] |
B. | \[N{{H}_{2}}OH\] |
C. | \[{{(C{{H}_{3}})}_{3}}N\] |
D. | \[H{{N}_{3}}\] |
Answer» E. | |
1819. |
Aniline when treated with conc. \[HN{{O}_{3}}\] gives [KCET 1996] |
A. | |
B. | |
C. | |
D. | |
Answer» D. | |
1820. |
Aniline when treated with \[HN{{O}_{2}}\] and HCl at \[{{0}^{o}}C\] gives [CPMT 1982, 89; RPMT 2000] |
A. | Phenol |
B. | Nitrobenzene |
C. | A diazo compound |
D. | None of these |
Answer» D. None of these | |
1821. |
In the reduction of nitrobenzene, which of the following is the intermediate [CPMT 1999] |
A. | \[{{C}_{6}}{{H}_{5}}N=O\] |
B. | \[{{C}_{6}}{{H}_{5}}NH-NH-{{C}_{6}}{{H}_{5}}\] |
C. | \[{{C}_{6}}{{H}_{5}}-N=N-{{C}_{6}}{{H}_{5}}\] |
D. | \[{{C}_{6}}{{H}_{5}}N=\overset{O}{\mathop{\overset{\uparrow }{\mathop{N}}\,}}\,-{{C}_{6}}{{H}_{5}}\] |
Answer» B. \[{{C}_{6}}{{H}_{5}}NH-NH-{{C}_{6}}{{H}_{5}}\] | |
1822. |
Which of the following compounds does not react with \[NaN{{O}_{2}}\] and HCl [KCET 1996] |
A. | \[{{C}_{6}}{{H}_{5}}OH\] |
B. | \[{{C}_{6}}{{H}_{5}}N{{H}_{2}}\] |
C. | \[{{(C{{H}_{3}})}_{3}}CN{{O}_{2}}\] |
D. | \[{{(C{{H}_{3}})}_{3}}CHN{{O}_{2}}\] |
Answer» D. \[{{(C{{H}_{3}})}_{3}}CHN{{O}_{2}}\] | |
1823. |
Which of the following is most basic [MP PMT 1999] |
A. | \[{{C}_{6}}{{H}_{5}}N{{H}_{2}}\] |
B. | \[{{(C{{H}_{3}})}_{2}}NH\] |
C. | \[{{(C{{H}_{3}})}_{3}}N\] |
D. | \[N{{H}_{3}}\] |
Answer» C. \[{{(C{{H}_{3}})}_{3}}N\] | |
1824. |
The following compound can be classified as N-N dimethyl propanamine, N-methyl aniline and aniline [Bihar MEE 1996] |
A. | Primary, secondary, tertiary |
B. | Primary, tertiary, secondary |
C. | Secondary, tertiary, primary |
D. | Tertiary, primary, secondary |
E. | None of these |
Answer» F. | |
1825. |
The fusion of sodium with amine gives mainly [MP PMT 1999; CPMT 2002] |
A. | NaCN |
B. | \[Na{{N}_{3}}\] |
C. | NaSCN |
D. | \[NaN{{O}_{2}}\] |
Answer» B. \[Na{{N}_{3}}\] | |
1826. |
The amine which does not react with acetyl chloride is or Which of the following cannot be acetylated [MP PET 1999; MP PMT 1999] |
A. | \[C{{H}_{3}}N{{H}_{2}}\] |
B. | \[{{(C{{H}_{3}})}_{2}}NH\] |
C. | \[{{(C{{H}_{3}})}_{3}}N\] |
D. | None of these |
Answer» D. None of these | |
1827. |
The alkyl cyanides when hydrolysed to the corresponding acid, the gas evolved is |
A. | \[{{N}_{2}}\] |
B. | \[{{O}_{2}}\] |
C. | \[N{{H}_{3}}\] |
D. | \[C{{O}_{2}}\] |
Answer» D. \[C{{O}_{2}}\] | |
1828. |
The reaction of \[HN{{O}_{2}}\] with 'A' gives quaternary ammonium salt. A is [MP PMT 1997] |
A. | Methyl amine |
B. | Dimethyl amine |
C. | Trimethyl amine |
D. | Aniline |
Answer» D. Aniline | |
1829. |
Which of the following has the smell of bitter almonds |
A. | Nitromethane |
B. | Nitroethane |
C. | Nitrobenzene |
D. | Aniline |
Answer» D. Aniline | |
1830. |
Which of the following is not used as an explosive [MP PET 1996] |
A. | Trinitrotoluene |
B. | Trinitrobenzene |
C. | Picric acid |
D. | Nitrobenzene |
Answer» E. | |
1831. |
Which statement is not correct [MP PMT 1995] |
A. | Amines form hydrogen bond |
B. | Ethyl amine has higher boiling point than propane |
C. | Methyl amine is more basic than ammonia |
D. | Dimethyl amine is less basic than methyl amine |
Answer» E. | |
1832. |
Aniline on treatment with conc. \[HN{{O}_{3}}+\] conc. \[{{H}_{2}}S{{O}_{4}}\] mixture yields [AIIMS 1992] |
A. | o- and p-nitroanilines |
B. | m-nitroanilines |
C. | A black tarry matter |
D. | No reaction |
Answer» D. No reaction | |
1833. |
Aniline reacts with alkyl halide to give [KCET 1984] |
A. | Amino compound |
B. | Tertiary compound |
C. | Quaternary ammonium compound |
D. | Azomethane |
Answer» D. Azomethane | |
1834. |
Unpleasant smelling carbylamines are formed by heating alkali and chloroform with [KCET 1987, 2000, 01] |
A. | Any amine |
B. | Any aliphatic amine |
C. | Any aromatic amine |
D. | Any primary amine |
Answer» E. | |
1835. |
Aniline on treatment with excess of bromine water gives [AFMC 1990; MP PMT 1991; RPMT 1997] |
A. | Aniline bromide |
B. | o-bromoaniline |
C. | p-bromoaniline |
D. | 2, 4, 6-tribromoaniline |
Answer» E. | |
1836. |
Among the following compounds nitrobenzene, benzene, aniline and phenol, the strongest basic behaviour in acid medium is exhibited by [KCET 1993] |
A. | Phenol |
B. | Aniline |
C. | Nitrobenzene |
D. | Benzene |
Answer» C. Nitrobenzene | |
1837. |
Correct order of increasing basicity is [CBSE PMT 1992] |
A. | \[N{{H}_{3}}<{{C}_{6}}{{H}_{5}}N{{H}_{2}}<{{({{C}_{2}}{{H}_{5}})}_{2}}NH<{{C}_{2}}{{H}_{5}}N{{H}_{2}}<{{({{C}_{2}}{{H}_{5}})}_{3}}N\] |
B. | \[{{C}_{6}}{{H}_{5}}N{{H}_{2}}<N{{H}_{3}}<{{({{C}_{2}}{{H}_{5}})}_{3}}N<{{({{C}_{2}}{{H}_{5}})}_{2}}NH<{{C}_{2}}{{H}_{5}}N{{H}_{2}}\] |
C. | \[{{C}_{6}}{{H}_{5}}N{{H}_{2}}<N{{H}_{3}}<{{C}_{2}}{{H}_{5}}N{{H}_{2}}<{{({{C}_{2}}{{H}_{5}})}_{3}}N<{{({{C}_{2}}{{H}_{5}})}_{2}}NH\] |
D. | \[{{C}_{6}}{{H}_{5}}N{{H}_{2}}<{{({{C}_{2}}{{H}_{5}})}_{3}}N<N{{H}_{3}}<{{C}_{2}}{{H}_{5}}N{{H}_{2}}<{{({{C}_{2}}{{H}_{5}})}_{2}}NH\] |
Answer» E. | |
1838. |
The alkyl cyanides are |
A. | Acidic |
B. | Basic |
C. | Neutral |
D. | Amphoteric |
Answer» B. Basic | |
1839. |
The decreasing order of the basic character of the three amines and ammonia is [MP PET/PMT 1988; KCET 1990] |
A. | \[N{{H}_{3}}>C{{H}_{3}}N{{H}_{2}}>{{C}_{2}}{{H}_{5}}N{{H}_{2}}>{{C}_{6}}{{H}_{5}}N{{H}_{2}}\] |
B. | \[{{C}_{2}}{{H}_{5}}N{{H}_{2}}>C{{H}_{3}}N{{H}_{2}}>N{{H}_{3}}>{{C}_{6}}{{H}_{5}}N{{H}_{2}}\] |
C. | \[{{C}_{6}}{{H}_{5}}N{{H}_{2}}>{{C}_{2}}{{H}_{5}}N{{H}_{2}}>C{{H}_{3}}N{{H}_{2}}>N{{H}_{3}}\] |
D. | \[C{{H}_{3}}N{{H}_{2}}>{{C}_{2}}{{H}_{5}}N{{H}_{2}}>{{C}_{6}}{{H}_{5}}N{{H}_{2}}>N{{H}_{3}}\] |
Answer» C. \[{{C}_{6}}{{H}_{5}}N{{H}_{2}}>{{C}_{2}}{{H}_{5}}N{{H}_{2}}>C{{H}_{3}}N{{H}_{2}}>N{{H}_{3}}\] | |
1840. |
Nitrobenzene on reduction by zinc and \[N{{H}_{4}}Cl\] gives [CPMT 1989, 94; BHU 1996; Pb. PMT 1999] |
A. | Aniline |
B. | Nitrosobenzene |
C. | Hydrazobenzene |
D. | Phenylhydroxyl amine |
Answer» E. | |
1841. |
Methyl amine reacts with \[HN{{O}_{2}}\] giving [RPMT 1997] |
A. | \[C{{H}_{3}}O-N=O\] |
B. | \[C{{H}_{3}}-O-C{{H}_{3}}\] |
C. | \[C{{H}_{3}}OH\] |
D. | A and B both |
Answer» E. | |
1842. |
Primary and secondary amines are distinguished by [AMU 1988; MP PMT 1996] |
A. | \[B{{r}_{2}}/KOH\] |
B. | \[HCl{{O}_{4}}\] |
C. | \[HN{{O}_{2}}\] |
D. | \[N{{H}_{3}}\] |
Answer» D. \[N{{H}_{3}}\] | |
1843. |
Which one of the following will give a primary amine on hydrolysis [BHU 1982] |
A. | Nitroparaffin |
B. | Alkyl cyanide |
C. | Oxime |
D. | Alkyl isocyanide |
Answer» E. | |
1844. |
The end product of the reactions is \[{{C}_{2}}{{H}_{5}}N{{H}_{2}}\xrightarrow{HN{{O}_{2}}}A\xrightarrow{PC{{l}_{5}}}B\xrightarrow{H.N{{H}_{2}}}C\] [CPMT 1988, 89, 93; DCE 1999; JIPMER 2000] |
A. | Ethyl cyanide |
B. | Ethyl amine |
C. | Methyl amine |
D. | Acetamide |
Answer» C. Methyl amine | |
1845. |
Identify the product Z in the series \[C{{H}_{3}}CN\xrightarrow{Na+{{C}_{2}}{{H}_{5}}OH}X\xrightarrow{HN{{O}_{2}}}Y\underset{{{H}_{2}}S{{O}_{4}}}{\mathop{\xrightarrow{{{K}_{2}}C{{r}_{2}}{{O}_{7}}}}}\,Z\] [AIIMS 1983; JIPMER 2001] |
A. | \[C{{H}_{3}}CHO\] |
B. | \[C{{H}_{3}}CON{{H}_{2}}\] |
C. | \[C{{H}_{3}}COOH\] |
D. | \[C{{H}_{3}}C{{H}_{2}}NHOH\] |
Answer» D. \[C{{H}_{3}}C{{H}_{2}}NHOH\] | |
1846. |
The compound which on reaction with aqueous nitrous acid on \[HN{{O}_{2}}\] at low temperature produces an oily nitrosoamine is [IIT 1981; CPMT 1989; MP PET/PMT 1998; Kurukshetra CEE 1998; MP PMT 2001] |
A. | Diethylamine |
B. | Ethylamine |
C. | Aniline |
D. | Methylamine |
Answer» B. Ethylamine | |
1847. |
Nitro group in nitrobenzene is a [MNR 1986] |
A. | Ortho director |
B. | Meta director |
C. | Para director |
D. | Ortho and para director |
Answer» C. Para director | |
1848. |
When methyl cyanide is hydrolysed in presence of alkali, the product is [MP PMT 1993; BCECE 2005] |
A. | Acetamide |
B. | Methane |
C. | \[C{{O}_{2}}+{{H}_{2}}O\] |
D. | Acetic acid |
Answer» E. | |
1849. |
When chloroform reacts with ethyl amine in presence of alcoholic KOH, the compound formed is [CPMT 1983; MP PMT 1993; CBSE PMT 1997; BHU 1999; AIEEE 2002] |
A. | Ethyl cyanide |
B. | Ethyl isocyanide |
C. | Formic acid |
D. | An amide |
Answer» C. Formic acid | |
1850. |
On heating acetamide in presence of \[{{P}_{2}}{{O}_{5}},\] which of the following is formed [MP PMT 1992; MP PET 1994; Kurukshetra CEE 1998] |
A. | Ammonium acetate |
B. | Acetonitrile |
C. | \[N{{H}_{3}}\] |
D. | Methylamines |
Answer» C. \[N{{H}_{3}}\] | |