The IUPAC name of the below compound is:
1. 3,4-Dimethylhexane –1,3,5-triol
2. 3,5-Dimethylhexane –1,1,5-triol
3. 3,5-Dimethylhexane –1,3,5-triol
4. 3,1-Dimethylhexane –1,3,5-triol
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 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 |
The reaction of hydrogen iodide with methoxybenzene gives:
1. | Phenol | 2. | Iodomethane |
3. | Phenol and Iodomethane | 4. | None of the above |