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Which of the following alcohols will sho...

Which of the following alcohols will show positive iodoform test?

A

`CH_(3)-overset(OH)overset(|)(CH)-CH_(2)-NO_(2)`

B

`CH_(3)-overset(OH)overset(|)(CH)-CH_(2)-overset(O)overset(||)(C)-OH`

C

`ICH_(2)-overset(OH)overset(|)(CH)-CH_(2)CH_(3)`

D

None of these

Text Solution

AI Generated Solution

The correct Answer is:
To determine which alcohols will show a positive iodoform test, we need to understand the requirements for this test. The iodoform test is used to identify the presence of a methyl ketone (RCOCH3) or a secondary alcohol that can be oxidized to a methyl ketone. The test involves the reaction of the alcohol with iodine and sodium hydroxide (NaOH), resulting in the formation of a yellow precipitate of iodoform (CHI3) if the test is positive. ### Step-by-Step Solution: 1. **Understand the Iodoform Test**: - The iodoform test is a qualitative test used to identify methyl ketones (RCOCH3) or secondary alcohols that can be oxidized to methyl ketones. - The reaction involves iodine (I2) and sodium hydroxide (NaOH), which leads to the formation of a yellow precipitate of iodoform (CHI3) if the test is positive. 2. **Identify the Structure of Alcohols**: - Analyze the structures of the given alcohols (let's assume we have five options: A, B, C, D, and E). - Look for the presence of the functional groups that can lead to a positive iodoform test, specifically the methyl ketone structure or secondary alcohols that can be oxidized to a methyl ketone. 3. **Evaluate Each Alcohol**: - For each alcohol, check if it has: - A methyl group adjacent to the hydroxyl group (for secondary alcohols). - A structure that can be oxidized to a methyl ketone. - Alcohol A: Check if it has the required structure. - Alcohol B: Check if it has the required structure. - Alcohol C: Check if it has the required structure. - Alcohol D: Check if it has the required structure. - Alcohol E: Check if it has the required structure. 4. **Determine Positive or Negative Test**: - If an alcohol has the required structure, it will give a positive iodoform test, resulting in a yellow precipitate. - If it does not have the required structure, it will give a negative test. 5. **Conclusion**: - After evaluating all options, identify which alcohol(s) showed a positive iodoform test based on the presence of the methyl ketone or secondary alcohol structure. ### Final Answer: - The correct alcohol that shows a positive iodoform test is **Option C**.

To determine which alcohols will show a positive iodoform test, we need to understand the requirements for this test. The iodoform test is used to identify the presence of a methyl ketone (RCOCH3) or a secondary alcohol that can be oxidized to a methyl ketone. The test involves the reaction of the alcohol with iodine and sodium hydroxide (NaOH), resulting in the formation of a yellow precipitate of iodoform (CHI3) if the test is positive. ### Step-by-Step Solution: 1. **Understand the Iodoform Test**: - The iodoform test is a qualitative test used to identify methyl ketones (RCOCH3) or secondary alcohols that can be oxidized to methyl ketones. - The reaction involves iodine (I2) and sodium hydroxide (NaOH), which leads to the formation of a yellow precipitate of iodoform (CHI3) if the test is positive. ...
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Knowledge Check

  • Which of the following alcohols will not give iodoform test ?

    A
    B
    `CH_3-CH_2-OH`
    C
    D
  • Which of the following compounds will give positive Tollen's test?

    A
    `CH_(3)-overset(O)overset(||)(C)-H`
    B
    C
    D
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