If Compound A (C₄H₈) is treated with H₂O/H₂SO₄ and forms an optically inactive C₄H₁₀O, what is the structure of A?
1. | CH3CH2CH=CH2 | 2. | CH3CH=CHCH3 |
3. | (CH3)2C=CH2 | 4. | ![]() |
Compound A is:
1. | 2. | ||
3. | 4. |
The major product in the above-mentioned reaction is:
1. | |
2. | |
3. | |
4. |
The increasing order of the reactivity of the following compounds towards electrophilic aromatic substitution reaction is:
1. | III < I < II | 2. | III < II < I |
3. | II < I < III | 4. | II < III < I |
In the following reaction,
\(\mathrm{ CH_{3}C\equiv CH\xrightarrow[Red \ hot \ iron \ tube]{873 K} \ A}\)
The number of () bonds present in the product (A) is:
1. | 21 | 2. | 9 |
3. | 24 | 4. | 18 |
3-Phenylpropene on reaction with HBr gives (as a major product)-
1.
2.
3.
4.
1,2-dibromopropane on treatment with X moles of followed by treatment with ethyl bromine gave a pent-2-yne. The value of X is -
1. 1
2. 2
3. 3
4. 4
The product X in the above mentioned reaction is:
1. | ![]() |
2. | ![]() |
3. | ![]() |
4. | ![]() |
The reaction among the following that proceeds through an electrophilic substitution reaction is:
1. | |
2. | |
3. | |
4. |
The most suitable reagent for the following conversion is-
1. | Hg2+/ H+, H2O | 2. | Na/liquid NH3 |
3. | H2, Pd/C, quinoline | 4. | Zn/HCl |