Iodoform reaction is given by (a) 2 -pentanone (b) 3-pentanone (c) 2 -propanol (d) Both (a) and (c)

Short Answer

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(a) 2-Pentanone (b) 3-Pentanone (c) 2-Propanol (d) Both (a) and (c) Answer: (d) Both (a) and (c)

Step by step solution

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1. Identify Methyl Ketone Group

Before we start the analysis, let's recall the structure of a methyl ketone group. A methyl ketone has the general structure CH3CO-R, with one carbonyl group and a methyl group directly bonded to the carbonyl carbon.
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2. 2-Pentanone

The structure of 2-pentanone is: CH3CH2COCH2CH3. Here, we can observe that it contains a methyl ketone group (CH3CO-), thus 2-pentanone will undergo iodoform reaction.
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3. 3-Pentanone

The structure of 3-pentanone is: CH3CH2COCH(CH3)CH3. In this case, there is no CH3CO- group present as the carbonyl carbon is not bonded to a methyl group. Thus, 3-pentanone will not undergo iodoform reaction.
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4. 2-Propanol

The structure of 2-propanol is: CH3CH(OH)CH3. Even though it isn't a ketone, it can be easily oxidized to a methyl ketone (acetone: CH3COCH3) under basic conditions, which is a condition for iodoform reaction. Therefore, 2-propanol can undergo iodoform reaction.
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5. Answer

According to the analysis above, (a) 2-pentanone and (c) 2-propanol can undergo iodoform reaction. Thus, the correct answer is (d) Both (a) and (c).

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