Match the structures given in Column I with the names in Column II.

Column I Column II
A.   1. 4-Bromopent-2-ene
B.   2. 4-Bromo-3-methylpent-2-ene
C.   3. 1-Bromobut-2-ene
D.   4. 1-Bromo-2-methylpent-2-ene

Codes:

A B C D
1. 2 3 4 1
2. 1 2 3 4
3. 1 4 3 2
4. 4 1 3 2
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The correct IUPAC name for the following structure is:
 
1. 2-Chloro-3-methylbutane

2. 3-Chloro-2-methylbutane

3. 2-Chloro-1-methylbutane

4. 3-Chloro-1-methylbutane

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p-Dichlorobenzene has a higher melting point than those of o- and m-isomers because :

1. More energy is required to break the crystal lattice of m-dichlorobenzene
2. More energy is required to break the crystal lattice of p-dichlorobenzene
3. More energy is required to break the crystal lattice of o-dichlorobenzene
4. None of the above
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Match the structures of compounds given in Column I with the classes of compounds given in Column II.

Column I Column II
A.   1. Aryl halide
B.   2. Alkyl halide
C.   3. Vinyl halide
D. 4. Allylic halide

Codes:

A B C D
1. 2 4 1 3
2. 3 4 1 2
3. 1 4 3 2
4. 4 1 3 2
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Which of the following molecules has the highest melting point?

1. Chlorobenzene

2. o-Dichlorobenzene

3. m-Dichlorobenzene

4. p-Dichlorobenzene

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The C-Cl bond of chlorobenzene in comparison to the C-Cl bond in methyl chloride is:

1. Shorter and weaker

2. Shorter and stronger

3. Longer and weaker

4. Longer and stronger

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What is the correct IUPAC name of the below mentioned compound?

  

1. 1−Chloro−4−(1−iodophenyl)−3, 3−dimethylbut−1−ene
2. 1−Chloro−1−(4−iodophenyl)−3, 3−dimethylbut−1−ene
3. 1−Chloro−2−(3−iodophenyl)−3, 3−dimethylbut−1−en
4. 4−Chloro−1−(1−iodophenyl)−1, 1−dimethylbut−3−ene
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Which of the following C-X bonds is the strongest?

1. \(\mathrm{CH}_3 \mathrm{Br} \) 2. \(\mathrm{CH}_3 \mathrm{Cl} \)
3. \(\mathrm{CH}_3 \mathrm{I} \) 4. \(\mathrm{CH}_3 \mathrm{~F}\)
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Which of the following compounds has the lowest boiling point?

1. Pentyl chloride

2. tertiary-Butyl chloride

3. Isobutyl chloride

4. n-Butyl chloride

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What is the correct order of boiling points for alkyl halides?

1. C2H5Cl > C2H5Br > C2H5I

2. C2H5I > C2H5Br > C2H5Cl  

3. C2H5I > C2H5Cl > C2H5Br

4. C2H5Br > C2H5I > C2H5Cl

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