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This section includes 84 Mcqs, each offering curated multiple-choice questions to sharpen your Chemistry knowledge and support exam preparation. Choose a topic below to get started.
1. |
Butanone is a four-carbon compound with the functional group |
A. | carboxylic acid |
B. | aldehyde |
C. | ketone |
D. | alcohol |
Answer» D. alcohol | |
2. |
Organic compounds will always contain |
A. | carbon |
B. | hydrogen |
C. | nitrogen |
D. | sulphur |
Answer» B. hydrogen | |
3. |
Which is a general formula of alkenes? |
A. | \[{{C}_{n}}{{H}_{2n+2}}\] |
B. | \[{{C}_{n}}{{H}_{2n}}\], |
C. | \[{{C}_{n}}{{H}_{2n-2}}\] |
D. | None of these |
Answer» C. \[{{C}_{n}}{{H}_{2n-2}}\] | |
4. |
\[0.0833\,mol\] of carbohydrate of empirical formula \[C{{H}_{2}}O\] contain \[1g\] of hydrogen. The molecular formula of the carbohydrate is [DCE 2003; BVP 2004] |
A. | \[{{C}_{5}}{{H}_{10}}{{O}_{5}}\] |
B. | \[{{C}_{3}}{{H}_{4}}{{O}_{3}}\] |
C. | \[{{C}_{12}}{{H}_{22}}{{O}_{11}}\] |
D. | \[{{C}_{6}}{{H}_{12}}{{O}_{6}}\] |
Answer» E. | |
5. |
If 0.228 g of silver salt of dibasic acid gave a residue of 0.162g of silver on ignition then molecular weight of the acid is [AIIMS 2000] |
A. | 70 |
B. | 80 |
C. | 90 |
D. | 100 |
Answer» D. 100 | |
6. |
An organic compound contains 49.3% carbon 6.84% hydrogen and its vapour density is 73. Molecular formula of the compound is [MP PET 2000; Kerala PMT 2004; Pb. CET 2004] |
A. | \[{{C}_{3}}{{H}_{5}}{{O}_{2}}\] |
B. | \[{{C}_{6}}{{H}_{10}}{{O}_{4}}\] |
C. | \[{{C}_{3}}{{H}_{10}}{{O}_{2}}\] |
D. | \[{{C}_{4}}{{H}_{10}}{{O}_{2}}\] |
Answer» C. \[{{C}_{3}}{{H}_{10}}{{O}_{2}}\] | |
7. |
IUPAC name of the compound \[C{{H}_{3}}-C{{H}_{2}}-\overset{C{{H}_{3}}}{\mathop{\overset{|\,\,\,\,}{\mathop{CH}}\,}}\,-C{{H}_{2}}-\underset{\underset{\underset{\overset{\underset{\begin{matrix} C{{H}_{3}} & C{{H}_{3}}\,\,\,\\ \end{matrix}}{\mathop{\hat{\ }}}\,}{\mathop{{}}}\,}{\mathop{CH\,\,\,\,\,\,\,\,}}\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}{\mathop{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}}\,}{\mathop{CH\,\,\,-\,\,C{{H}_{2}}-C{{H}_{2}}C{{H}_{3}}}}\,\] [Orissa JEE 2003] |
A. | 4-isopropyl 1-6-methyl octane |
B. | 3- methyl-5-(1?-methylethyl) octane |
C. | 3-methyl-5-isopropyl octane |
D. | 6-methyl-4-(1?methylethyl) octane |
Answer» C. 3-methyl-5-isopropyl octane | |
8. |
A hydrocarbon contains 10.5 gm carbon and 1gm hydrogen. Its 2.4 gm has 1 litre volume at 1 atm and \[{{127}^{o}}C\], hydrocarbon is [UPSEAT 2003] |
A. | \[{{C}_{6}}{{H}_{7}}\] |
B. | \[{{C}_{6}}{{H}_{8}}\] |
C. | \[{{C}_{5}}{{H}_{6}}\] |
D. | None of these |
Answer» B. \[{{C}_{6}}{{H}_{8}}\] | |
9. |
How many H-atoms are present in 0.046 g of ethanol [DCE 2003] |
A. | \[6\times {{10}^{20}}\] |
B. | \[1.2\times {{10}^{21}}\] |
C. | \[3\times {{10}^{21}}\] |
D. | \[3.6\times {{10}^{21}}\] |
Answer» E. | |
10. |
The IUPAC name of the compound \[C{{H}_{3}}-CH({{C}_{2}}{{H}_{5}})-CH=CH-C{{H}_{3}}\]is [BHU 2002] |
A. | 4-ethyl-2-pentene |
B. | 4-methyl 2-hexene |
C. | 3-ethyl-2-pentene |
D. | 2-ethyl-3-pentene |
Answer» C. 3-ethyl-2-pentene | |
11. |
The IUPAC name of \[C{{H}_{3}}-\overset{OH}{\mathop{\overset{|\,\,\,\,\,}{\mathop{CH}}\,}}\,-C{{H}_{2}}-\overset{\overset{C{{H}_{3}}\,\,\,\,\,\,\,\,}{\mathop{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}}\,}{\mathop{CHCHO}}\,\] is [JIPMER 2002] |
A. | 4 Hydroxy-2-methylpentanal |
B. | 2-hydroxy-4 methyl pentanal |
C. | 2-methyl pent-4-ol-1-al |
D. | None of these |
Answer» B. 2-hydroxy-4 methyl pentanal | |
12. |
The IUPAC name of thecompound \[C{{H}_{2}}=CH-C{{H}_{2}}-C{{H}_{2}}-C\equiv CH\]is [CBSE PMT 2002; MP PMT 2003] |
A. | 1, 5-hexenyne |
B. | 1-hexyne-5-ene |
C. | 1, 5-hexynene |
D. | 1-hexene-5-yne |
Answer» E. | |
13. |
IUPAC name of compound is \[C{{H}_{3}}-C{{H}_{2}}-CH(C{{H}_{3}})-C{{H}_{2}}-COCl\] [RPMT 2002] |
A. | 3-methyl pentanoyl chloride |
B. | 3-methyl butanoyl chloride |
C. | 1-chloro-3-methyl pentanol |
D. | None of these |
Answer» B. 3-methyl butanoyl chloride | |
14. |
The IUPAC name of picric acid is [KCET 2002] |
A. | 2,4,6-trinitrophenol |
B. | 2,4,6-trinitrobenzoic acid |
C. | 4-nitrophenol |
D. | None of these |
Answer» B. 2,4,6-trinitrobenzoic acid | |
15. |
General formula of paraffin is [RPMT 2002] |
A. | \[{{C}_{n}}{{H}_{2n}}\] |
B. | \[{{C}_{n}}{{H}_{2n-2}}\] |
C. | \[{{C}_{n}}{{H}_{2n+2}}\] |
D. | \[{{C}_{2n}}{{H}_{2n}}\] |
Answer» D. \[{{C}_{2n}}{{H}_{2n}}\] | |
16. |
The IUPAC name of \[C{{H}_{3}}C\equiv CCH\,{{(C{{H}_{3}})}_{2}}\]is [UPSEAT 2001] |
A. | 4 methyl-2 pentyne |
B. | 4, 4-dimethyl-2-butyne |
C. | Methyl isopropyl acetylene |
D. | 2-methyl-4-pentyne |
Answer» B. 4, 4-dimethyl-2-butyne | |
17. |
The IUPAC name of the compound \[C{{H}_{3}}-\underset{C{{H}_{3}}}{\mathop{\underset{|\,\,\,\,}{\mathop{C\,}}\,=}}\,C{{H}_{2}}C{{H}_{2}}OH\] is [BHU 2001] |
A. | 2-methyl-2-butenol |
B. | 2-methyl-3-butenol |
C. | 3-methyl-2-butenol |
D. | 3-methyl- but-2-ene-1-ol |
Answer» E. | |
18. |
IUPAC name of the following compound is [AIIMS 2003] |
A. | 3-methyl cyclohexene |
B. | 1-methyl cyclohex-2-ene |
C. | 6-methyl cyclohexene |
D. | 1-methyl cyclohex-5-ene |
Answer» B. 1-methyl cyclohex-2-ene | |
19. |
The IUPAC name of compound \[C{{H}_{3}}-C{{(C{{H}_{3}})}_{2}}-C{{H}_{2}}-CH=C{{H}_{2}}\] is [CPMT 2001] |
A. | 2, 2-dimethyl pent-4-ene |
B. | 2, 2 dimethyl-2-pentene |
C. | 1, 1, 1-trimethyl but-3-ene |
D. | 4, 4-dimethyl pent-1-ene |
Answer» E. | |
20. |
Which C-atoms is the most electronegative in this structure \[\overset{\text{III}}{\mathop{C{{H}_{3}}}}\,-\overset{\text{II}}{\mathop{C{{H}_{2}}}}\,-C\equiv \overset{\text{I}}{\mathop{CH}}\,\] [CPMT 2001] |
A. | I |
B. | II |
C. | III |
D. | All are equal electronegative |
Answer» B. II | |
21. |
The IUPAC name of \[{{(C{{H}_{3}})}_{2}}CH-C{{H}_{2}}-C{{H}_{2}}Br\] is [MH CET 2001; CBSE PMT 2001; Pb. PMT 2004] |
A. | 1-bromo pentane |
B. | 2-methyl and 4 bromo butane |
C. | 1-bromo and 3-methyl butane |
D. | 2-methyl and 3 bromo propane |
Answer» D. 2-methyl and 3 bromo propane | |
22. |
IUPAC name of the compoundis \[C{{H}_{3}}-\underset{C{{H}_{3}}}{\mathop{\underset{|\,\,\,\,\,\,}{\mathop{\underset{C{{H}_{2}}}{\mathop{\underset{|\,\,\,\,\,}{\mathop{CH}}\,}}\,}}\,}}\,-C{{H}_{2}}-CH(OH)-C{{H}_{3}}\] is [DPMT 1985; MP PMT 1987; AFMC 1997] |
A. | 4-ethyl-2-pentanol |
B. | 4-methyl-2-hexanol |
C. | 2-ethyl-2-pentanol |
D. | 3-methyl-2-hexanol |
Answer» C. 2-ethyl-2-pentanol | |
23. |
IUPAC name of the \[{{(C{{H}_{3}})}_{2}}CHCH{{(C{{H}_{3}})}_{2}}\] is [MP PMT 1986] |
A. | 1, 1, 2, 3-tetramethylethane |
B. | 1, 2-di-isopropylethane |
C. | 2, 3-dimethylbutane |
D. | 2, 3, 3-trimethylbutane |
Answer» D. 2, 3, 3-trimethylbutane | |
24. |
Which of the following compound has the functional group \[-\text{ }OH\] |
A. | 1, 2-ethandiol |
B. | 2-butanone |
C. | Nitrobenzene |
D. | Ethanal |
Answer» B. 2-butanone | |
25. |
The IUPAC name of the compound \[CHO-{{(C{{H}_{2}})}_{4}}-COOH\] [DCE 1999] |
A. | Heaxan-1-al-6-oic acid |
B. | Formyl-hexanoic acid |
C. | Hexanal-1-carboxylic acid |
D. | Hexanoic acid 5-al-1 |
Answer» C. Hexanal-1-carboxylic acid | |
26. |
Which is the IUPAC name of \[C{{H}_{3}}\underset{{{C}_{2}}{{H}_{5}}\,\,\,\,\,\,\,\,\,\,}{\overset{{{C}_{2}}{{H}_{5}}\,\,\,\,\,\,\,\,\,\,}{\mathop{\underset{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}{\overset{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}{\mathop{C-C{{H}_{2}}Cl}}}\,}}}\,\] [KCET (Engg./Med.) 1999] |
A. | 1-chloro-2, 2-diethylpropane |
B. | 3-chloro-2, 2-diethylpropane |
C. | 1-chloro-2-ethyl-2 methylbutane |
D. | 1-chloro-2, 2-diethyl-2 methylethane |
Answer» D. 1-chloro-2, 2-diethyl-2 methylethane | |
27. |
The IUPAC name of the compound \[C{{H}_{3}}-\underset{OH\,\,\,\,\,\,\,}{\mathop{\underset{|\,\,\,\,\,\,\,\,\,\,\,\,\,}{\mathop{C=CH}}\,}}\,-C{{H}_{2}}-COOH\] is [AIIMS 1998] |
A. | Hydroxypentenoic acid |
B. | 4-hydroxy-3-pentenoic acid |
C. | 4-hydroxy-4-pentenoic acid |
D. | 4-hydroxy-4-methyl-3-butenoic acid |
Answer» C. 4-hydroxy-4-pentenoic acid | |
28. |
IUPAC name of \[C{{H}_{3}}-\underset{{{C}_{2}}{{H}_{5}}\,\,}{\mathop{\underset{|\,\,\,\,\,\,}{\mathop{\overset{H\,\,\,}{\mathop{\overset{|\,\,\,\,\,}{\mathop{C-}}\,}}\,}}\,}}\,\underset{C{{H}_{3}}\,\,\,\,\,\,\,\,\,}{\mathop{\underset{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}{\mathop{\overset{{{C}_{4}}{{H}_{9}}\,\,\,\,\,}{\mathop{\overset{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}{\mathop{C-C{{H}_{3}}}}\,}}\,}}\,}}\,\] is [BHU 1998; KCET (Engg./Med) 2000] |
A. | 2-butyl-2-methyl-3-ethylbutane |
B. | 2-ethyl-3, 3-dimethylheptane |
C. | 3, 4, 4-trimethylheptane |
D. | 3, 4, 4-trimethyloctane |
Answer» E. | |
29. |
The IUPAC name for the formula \[C{{H}_{3}}-\underset{C{{H}_{3}}\,\,\,}{\mathop{\underset{|\,\,\,\,\,\,\,\,\,}{\mathop{C=\overset{H}{\mathop{\overset{|}{\mathop{C}}\,}}\,}}\,}}\,-COOH\] [Pb. PMT 1998] |
A. | 2-methyl-2-butenoic acid |
B. | 3-methyl-3-butenoic acid |
C. | 3-methyl-2-butenoic acid |
D. | 2-methyl-3-butenoic acid |
Answer» D. 2-methyl-3-butenoic acid | |
30. |
IUPAC name of \[C{{H}_{3}}-CH=CH-C\equiv CH\] is [CPMT 1997] |
A. | Pent-2-en-4-yne |
B. | Pent-3-en-1-yne |
C. | Pent-3-yne-1-en |
D. | Pent-2-yne-1-en |
Answer» C. Pent-3-yne-1-en | |
31. |
The IUPAC name for \[C{{H}_{3}}CH=CHC{{H}_{2}}\underset{N{{H}_{2}}\,\,\,\,\,\,\,}{\mathop{\underset{|\,\,\,\,\,\,\,\,\,\,\,\,}{\mathop{CHC{{H}_{2}}}}\,}}\,COOH\] is [CBSE PMT 1995] |
A. | 5-aminohex-2-ene carboxylic acid |
B. | 5-amino-2-heptenoic acid |
C. | 3-amino-5-heptenoic acid |
D. | \[\beta -\] amino-\[\delta -\]heptenoic acid |
Answer» D. \[\beta -\] amino-\[\delta -\]heptenoic acid | |
32. |
IUPAC name of \[{{(C{{H}_{3}})}_{2}}CH-C{{H}_{2}}-C{{H}_{2}}Br\] is [CBSE PMT 1996] |
A. | 1-bromopentane |
B. | 2-methyl-4-bromobutane |
C. | 1-bromo-3-methylbutane |
D. | 2-methyl-3-romopropane |
Answer» D. 2-methyl-3-romopropane | |
33. |
The IUPAC name of succinic acid is [IIT-JEE 1994] |
A. | 1, 4-butanedioic acid |
B. | Dimethyl-2-acid |
C. | 1, 2-dimethyldioic acid |
D. | None of these |
Answer» B. Dimethyl-2-acid | |
34. |
The structure of 4-methyl pentene-2 is [BHU 1988] |
A. | \[{{(C{{H}_{3}})}_{2}}CH-C{{H}_{2}}CH=C{{H}_{2}}\] |
B. | \[{{(C{{H}_{3}})}_{2}}CH-CH=CH-C{{H}_{3}}\] |
C. | \[{{(C{{H}_{3}})}_{2}}CH-C{{H}_{2}}CH=CH-C{{H}_{3}}\] |
D. | \[{{(C{{H}_{3}})}_{2}}C=CHC{{H}_{2}}C{{H}_{3}}\] |
Answer» C. \[{{(C{{H}_{3}})}_{2}}CH-C{{H}_{2}}CH=CH-C{{H}_{3}}\] | |
35. |
The IUPAC name of \[C{{H}_{3}}-C{{H}_{2}}CH=\underset{C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\,}{\mathop{\underset{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}{\mathop{CC{{H}_{2}}OH}}\,}}\,\] will be [MP PET/PMT 1988] |
A. | 2-methyl pentyl alcohol |
B. | 4-methyl-3-pentene-ol |
C. | 2-methyl pent-2-ene-1-ol |
D. | 4-methyl pentyl alcohol |
Answer» D. 4-methyl pentyl alcohol | |
36. |
What is the correct IUPAC name for \[C{{H}_{3}}-\underset{C{{H}_{3}}}{\mathop{\underset{|\,\,\,\,}{\mathop{\overset{H\,\,\,}{\mathop{\overset{|\,\,\,\,\,}{\mathop{C-}}\,}}\,}}\,}}\,CH=CH-C{{H}_{2}}-\overset{O\,\,\,\,}{\mathop{\overset{||\,\,\,\,}{\mathop{C-}}\,}}\,OH\] [MP PET 1995] |
A. | 5-methyl-3-hexenoic acid |
B. | 5-carboxyl-2-methylpentene |
C. | 4-isopropyl-3-butenoic acid |
D. | None of above |
Answer» B. 5-carboxyl-2-methylpentene | |
37. |
IUPAC name of tertiary butyl alcohol is [CPMT 1994] |
A. | Butan-1-ol |
B. | Butan-2-ol |
C. | 2-methyl propan-1-ol |
D. | 2-methyl propan-2-ol |
Answer» E. | |
38. |
The IUPAC name of \[C{{H}_{3}}-\underset{OH}{\mathop{\underset{|\,\,\,\,}{\mathop{CH}}\,}}\,-C{{H}_{2}}-\underset{C{{H}_{3}}}{\mathop{\underset{|\,\,\,\,}{\mathop{CH}}\,}}\,-CHO\] will be [CBSE PMT 1992; JIPMER (Med.) 2002] |
A. | 4-hydroxy-1-methylpentanal |
B. | 4-hydroxy-2-methylpentanal |
C. | 3-hydroxy-2-methylpentanal |
D. | 3-hydroxy-3-methylpentanal |
Answer» C. 3-hydroxy-2-methylpentanal | |
39. |
The IUPAC name of \[C{{H}_{3}}C\equiv CCH{{(C{{H}_{3}})}_{2}}\] is [MNR 1993; Pb CET 2004] |
A. | 4-methyl-2-pentyne |
B. | 4, 4-dimethyl-2-butyne |
C. | Methyl isopropyl acetylene |
D. | 2-methyl-4-pentyne |
Answer» B. 4, 4-dimethyl-2-butyne | |
40. |
The IUPAC name of the compound \[C{{H}_{3}}-\underset{C{{H}_{3}}}{\mathop{\underset{|\,\,\,\,}{\mathop{CH}}\,}}\,-C{{H}_{2}}-C{{H}_{2}}-OH\] is [KCET 1990] |
A. | 1-pentanol |
B. | Pentanol |
C. | 2-methyl-4-butanol |
D. | 3-methyl-1-butanol |
Answer» E. | |
41. |
The IUPAC name of \[C{{H}_{3}}-C{{H}_{2}}-\underset{C{{H}_{3}}}{\mathop{\underset{|\,\,\,\,\,\,}{\mathop{C=}}\,}}\,C{{H}_{2}}\] is [EAMCET 1992; Pb. PMT 99] |
A. | 2-methylbutene-1 |
B. | 3-methylbutene-1 |
C. | Vinyl methylethane |
D. | Propylethene-1 |
Answer» B. 3-methylbutene-1 | |
42. |
In the structure \[^{1}{{H}_{3}}C-\underset{C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}{\mathop{\underset{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}{\mathop{\overset{C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}{\mathop{\overset{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}{\mathop{^{2}C-{{\,}^{3}}C{{H}_{2}}-{{\,}^{4}}C{{H}_{3}}}}\,}}\,}}\,}}\,\] Which one is quarternary carbon atom |
A. | C - 1 |
B. | C - 2 |
C. | C - 3 |
D. | C - 5 |
Answer» C. C - 3 | |
43. |
Write the IUPAC name of \[C{{H}_{3}}C{{H}_{2}}COOH\] [AFMC 2004] |
A. | Ethyl formic acid |
B. | Ethyl carboxylic acid |
C. | Ethane methanoic acid |
D. | Propanoic acid |
Answer» E. | |
44. |
IUPAC name of \[C{{H}_{2}}=CH-CH(C{{H}_{3}}C{{H}_{2}})\underset{Br}{\mathop{\underset{|\,\,\,\,\,}{\mathop{C=}}\,}}\,C{{H}_{2}}\] is ?..[JEE Orissa 2004] |
A. | 4-bromo-3-ethyl-1, 4-pentadiene |
B. | 2-bromo-3-ethyl-1, 4-pentadiene |
C. | 2-bromo-3-ethyl-1, 5-pentadiene |
D. | None of these |
Answer» C. 2-bromo-3-ethyl-1, 5-pentadiene | |
45. |
Which of the following compounds is not chiral[AIEEE 2004] |
A. | 1-chloro-2-methyl pentane |
B. | 2-chloropentane |
C. | 1-chloropentane |
D. | 3-chloro-2-methyl pentane |
Answer» B. 2-chloropentane | |
46. |
The IUPAC name of \[C{{H}_{3}}C{{H}_{2}}COC{{H}_{2}}C{{H}_{3}}\] is [EAMCET 1992] |
A. | 3-pentanone |
B. | 2-pentanone |
C. | Diethyl ketone |
D. | All the above |
Answer» B. 2-pentanone | |
47. |
Which compound is 2, 2, 3-trimethylhexane [IIT-JEE 1986] |
A. | \[\begin{matrix} C{{H}_{3}}\,\,C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\\ |\,\,\,\,\,\,\,\,\,\,|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\\ C{{H}_{3}}-C-CH-C{{H}_{2}}-C{{H}_{3}}\\ |\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\\ C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\\ \end{matrix}\] |
B. | \[\begin{matrix} \,\,\,C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\,\,C{{H}_{3}}\\ |\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,|\,\,\,\,\,\\ C{{H}_{3}}-C-C{{H}_{2}}-CH-C{{H}_{3}}\\ |\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\\ C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\\ \end{matrix}\] |
C. | \[\begin{matrix} C{{H}_{3}}\,C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\\ |\,\,\,\,\,\,\,\,|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\\ C{{H}_{3}}-C-CH-C{{H}_{2}}-C{{H}_{2}}-C{{H}_{3}}\\ |\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\\ C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\\ \end{matrix}\] |
D. | \[\begin{matrix} \,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,C{{H}_{3}}\\ \,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,|\\ C{{H}_{3}}-CH-C{{H}_{2}}-C{{H}_{2}}-C-C{{H}_{3}}\\ |\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,|\,\\ \,\,\,\,\,C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,C{{H}_{3}}\\ \end{matrix}\] |
Answer» D. \[\begin{matrix} \,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,C{{H}_{3}}\\ \,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,|\\ C{{H}_{3}}-CH-C{{H}_{2}}-C{{H}_{2}}-C-C{{H}_{3}}\\ |\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,|\,\\ \,\,\,\,\,C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,C{{H}_{3}}\\ \end{matrix}\] | |
48. |
The IUPAC name of \[C{{H}_{3}}C\equiv N\]is [CPMT 1990] |
A. | Acetonitrile |
B. | Ethanenitrile |
C. | Methyl cyanide |
D. | Cyanoethane |
Answer» C. Methyl cyanide | |
49. |
The compound formed in the positive test for nitrogen with the lassaigne solution of an organic compounds is [AIEEE 2004] |
A. | \[Fe{{(CN)}_{3}}\] |
B. | \[N{{a}_{3}}[Fe{{(CN)}_{6}}]\] |
C. | \[F{{e}_{4}}{{[Fe{{(CN)}_{6}}]}_{3}}\] |
D. | \[N{{a}_{4}}[Fe{{(CN)}_{5}}NOS]\] |
Answer» D. \[N{{a}_{4}}[Fe{{(CN)}_{5}}NOS]\] | |
50. |
The compound having only primary hydrogen atoms is [AIIMS 2004] |
A. | Isobutene |
B. | 2,3-Dimethylbutene |
C. | Cyclohexane |
D. | Propyne |
Answer» E. | |