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Among the following the one that gives p...

Among the following the one that gives positive iodoform test upon reaction with ` I _ 2 and NaOH ` is \

A

` CH_ 3 CH_2 CH (OH ) CH _ 2 CH _ 3 `

B

`CH_3 - CH (CH _ 3) CH _2 - OH `

C

`C_6 H _ 5 - CH_ 2 - CH _ 2 OH `

D

`PhCH (OH ) CH _ 3 `

Text Solution

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The correct Answer is:
To determine which compound gives a positive iodoform test upon reaction with I2 and NaOH, we need to identify the presence of a methyl ketone or a specific type of alcohol that can yield a methyl ketone upon oxidation. Here’s a step-by-step solution: ### Step 1: Understand the Iodoform Test The iodoform test is used to identify methyl ketones or certain alcohols. The general reaction involves the reaction of a carbonyl compound (specifically a methyl ketone or ethanol) with iodine (I2) in the presence of sodium hydroxide (NaOH), resulting in the formation of iodoform (CHI3), which is a yellow precipitate. ### Step 2: Identify the Requirements for a Positive Test 1. **Methyl Ketones**: Compounds of the form CH3C(=O)R, where R can be any alkyl group. 2. **Ethanol**: The only primary alcohol that gives a positive iodoform test. 3. **Specific Secondary Alcohols**: Alcohols that can be oxidized to form a methyl ketone. ### Step 3: Analyze Each Option Now, let's analyze the provided options: 1. **Option A**: CH3CH2CHOHCH2CH3 (2-degree alcohol) - This is a secondary alcohol but does not have the required structure to give a positive iodoform test. **Negative test**. 2. **Option B**: CH3CH(OH)CH3 (1-degree alcohol) - This is a primary alcohol. Only ethanol gives a positive test among primary alcohols. **Negative test**. 3. **Option C**: C6H5CH2CH2OH (1-degree alcohol) - This is also a primary alcohol and does not meet the criteria for a positive test. **Negative test**. 4. **Option D**: C6H5CHOHCH3 (2-degree alcohol) - This compound can be oxidized to form a methyl ketone (specifically, it has the structure CH3C(=O)R). Thus, it can give a positive iodoform test. **Positive test**. ### Conclusion The compound that gives a positive iodoform test is **Option D**: C6H5CHOHCH3. ---

To determine which compound gives a positive iodoform test upon reaction with I2 and NaOH, we need to identify the presence of a methyl ketone or a specific type of alcohol that can yield a methyl ketone upon oxidation. Here’s a step-by-step solution: ### Step 1: Understand the Iodoform Test The iodoform test is used to identify methyl ketones or certain alcohols. The general reaction involves the reaction of a carbonyl compound (specifically a methyl ketone or ethanol) with iodine (I2) in the presence of sodium hydroxide (NaOH), resulting in the formation of iodoform (CHI3), which is a yellow precipitate. ### Step 2: Identify the Requirements for a Positive Test 1. **Methyl Ketones**: Compounds of the form CH3C(=O)R, where R can be any alkyl group. 2. **Ethanol**: The only primary alcohol that gives a positive iodoform test. ...
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Knowledge Check

  • A compound that gives positive iodoform test is

    A
    1-pentanol
    B
    2-pentanone
    C
    3-pentanone
    D
    pentanal
  • A compound that gives positive iodoform test is

    A
    1-pentanol
    B
    2-pentanone
    C
    3-pentanone
    D
    pentanal
  • A compound that gives positive iodoform test is

    A
    1-pentanol
    B
    2-pentanone
    C
    3-pentanone
    D
    pentanal
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