The IUPAC name of the above compound is -
1. 2, 2, 2-Trimethylpentan-3-ol
2. 2, 2, 4-Trimethylpentan-3-ol
3. 2, 2, 3-Trimethylpentan-3-ol
4. 1, 1, 3-Trimethylpentan-3-ol
The IUPAC name of the above compound is:
1. 1-Phenylpropan-2-ol
2. 2-Phenylpropan-2-ol
3. 1-Phenylpropan-1-ol
4. 2-Phenylpropan-1-ol
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 -
The IUPAC name of
is -
1. Cyclopent-1-en-3-ol
2. Cyclopent-3-en-1-ol
3. Cyclopent-2-en-1-ol
4. Cyclopent-1-en-3-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