The IUPAC name of
1. 3,3-Diethylphenol
2. 2,2-Diethylphenol
3. 1,3-Diethylphenol
4. 2,3-Diethylphenol
The IUPAC name of the above compound is:
| 1. | 4 – Ethoxypropane | 2. | 3 – Ethoxypropane |
| 3. | 1 – Ethoxypropane | 4. | 2 – Ethoxypropane |
The IUPAC name of the following compound is:
1. 1-Ethoxy-3-methylpentane
2. 3-Ethoxy-1-methylpentane
3. 2-Ethoxy-3-methylpentane
4. 3-Ethoxy-2-methylpentane
The IUPAC name of the following compound is -
1. Cyclohexane ethanol
2. Cyclohexane methanol
3. Cyclohexyl ethanol
4. Cyclohexyl methanol
The structure and name of intermediate compound is -
| 1. |  Cumene hydroperoxide |
| 2. |  Cumene hydroperoxide |
| 3. |  Cumene hydroperoxide |
| 4. | None of these |
The IUPAC name of the following compound is:
1. Cyclopent-1-en-3-ol
2. Cyclopent-3-en-1-ol
3. Cyclopent-2-en-1-ol
4. Cyclopent-1-en-2-ol
"A" in the reaction below is:
| 1. | Chlorobenzene | 2. | 1,2-Dichlorobenzene |
| 3. | 1,3-dichlorobenzene | 4. | None of these |
The IUPAC name of above mentioned compound is:
1. 1-Chloro-3-ethylbutan-3-ol
2. 1-Chloro-3-ethylbutan-1-ol
3. 3-Chloro-3-ethylbutan-1-ol
4. 3-(Chloromethyl)pentan-1-ol
The proposed mechanism for hydration of ethene to yield ethanol is as follows:
The wrong step in the above mechanism is:
| 1. | Step 1 | 2. | Step 2 |
| 3. | Step 3 | 4. | Both steps 2 and 3 |
The reaction of 3-methylbutan-2-ol with HBr gives:
| 1. | 2-Bromo-3-methyl butane | 2. | 2-Bromo-2-methyl butane |
| 3. | 3-Bromo-2-methyl butane | 4. | 3-Bromo-3-methyl butane |
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