Compound `'X'` give positive test with `2,4` - DNP and with
`I_(2)//NaOH` compound (X) may be :

Options

A.
B.
C.
D. all of these

Explanation

To identify compound 'X' that gives positive tests with both 2,4-DNP and I2/NaOH, we can follow these steps:

### Step 1: Understand the Tests
- **2,4-DNP Test**: This test is used to identify carbonyl compounds (aldehydes and ketones). A positive test results in the formation of a colored precipitate (usually orange or yellow).
- **I2/NaOH Test**: This is known as the Iodoform test, which is positive for methyl ketones (compounds with the structure RCOCH3) and for ethanol (ethyl alcohol). A positive test results in the formation of iodoform (CHI3), which is a yellow precipitate.

### Step 2: Identify Possible Structures
- Since compound 'X' gives positive results for both tests, it must contain a carbonyl group (C=O).
- The possible structures that can give positive results for both tests include:
1. Acetone (CH3COCH3)
2. Acetaldehyde (CH3CHO)
3. Benzyl methyl ketone (C6H5COCH3)

### Step 3: Analyze Each Compound
1. **Acetone (CH3COCH3)**:
- Positive for 2,4-DNP test (forms a yellow/orange precipitate).
- Positive for Iodoform test (forms iodoform).

2. **Acetaldehyde (CH3CHO)**:
- Positive for 2,4-DNP test (forms a yellow/orange precipitate).
- Negative for Iodoform test (does not have a methyl ketone structure).

3. **Benzyl methyl ketone (C6H5COCH3)**:
- Positive for 2,4-DNP test (forms a yellow/orange precipitate).
- Positive for Iodoform test (forms iodoform).

### Step 4: Conclusion
- The compounds that can be identified as 'X' are **Acetone (CH3COCH3)** and **Benzyl methyl ketone (C6H5COCH3)**, as both give positive results for the tests mentioned.

### Final Answer
Compound 'X' may be **Acetone (CH3COCH3)** or **Benzyl methyl ketone (C6H5COCH3)**.

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